Item | Value |
---|---|
geneid | 2132 |
ensemblid | ENSG00000151348.16 |
hgncid | 3513 |
symbol | EXT2 |
name | exostosin glycosyltransferase 2 |
refseq_nuc | NM_207122.2 |
refseq_prot | NP_997005.1 |
ensembl_nuc | ENST00000533608.7 |
ensembl_prot | ENSP00000431173.2 |
mane_status | MANE Select |
chr | chr11 |
start | 44095678 |
end | 44251962 |
strand | + |
ver | v1.2 |
region | chr11:44095678-44251962 |
region5000 | chr11:44090678-44256962 |
regionname0 | EXT2_chr11_44095678_44251962 |
regionname5000 | EXT2_chr11_44090678_44256962 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 718 | 323 | 72 | 46 | 161 | 10 | 32 | 123 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
a0002 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
a0003 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
a0004 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
a0005 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
a0006 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | MCASV others(713): Show |
chr11 | 44090678 | 44256962 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2154 | 256 | 57 | 43 | 116 | 10 | 28 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0002 | 0/0 | 2154 | 44 | 0 | 1 | 41 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0003 | 0/0 | 2154 | 8 | 6 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0004 | 0/0 | 2154 | 6 | 3 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0007 | 0/0 | 2154 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0008 | 0/0 | 2154 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0009 | 0/0 | 2154 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0013 | 0/0 | 2154 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0001c0014 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0002c0005 | 0/0 | 2154 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0003c0006 | 0/0 | 2154 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0004c0012 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0005c0011 | 0/0 | 2154 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 | ||
a0006c0010 | 0/0 | 2154 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | ATGTG others(2149): Show |
chr11 | 44090678 | 44256962 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10036 | 57 | 5 | 10 | 33 | 1 | 8 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0002 | 0/1 | 10037 | 33 | 4 | 8 | 11 | 2 | 7 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0003 | 0/0 | 10036 | 28 | 12 | 2 | 11 | 0 | 3 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0004 | 0/0 | 10033 | 2 | 0 | 0 | 1 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0005 | 0/0 | 10038 | 19 | 2 | 5 | 9 | 2 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0006 | 0/0 | 10037 | 16 | 0 | 0 | 14 | 0 | 2 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0007 | 1/0 | 10037 | 12 | 7 | 2 | 0 | 2 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0008 | 0/0 | 10033 | 10 | 0 | 0 | 10 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0009 | 0/0 | 10036 | 12 | 0 | 0 | 12 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0010 | 0/0 | 10038 | 6 | 3 | 2 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0011 | 0/0 | 10036 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0012 | 0/0 | 10036 | 5 | 0 | 3 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0013 | 0/0 | 10038 | 4 | 1 | 2 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0014 | 0/0 | 10037 | 4 | 1 | 2 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0015 | 0/0 | 10033 | 4 | 4 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0018 | 0/0 | 10036 | 3 | 2 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0020 | 0/0 | 10035 | 2 | 1 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10030): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0021 | 0/0 | 10038 | 2 | 0 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0022 | 0/0 | 10037 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0023 | 0/0 | 10036 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0024 | 0/0 | 10037 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0025 | 0/0 | 10038 | 2 | 0 | 1 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0027 | 0/0 | 10036 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0028 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0030 | 0/0 | 10033 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0031 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0032 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0033 | 0/0 | 10034 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10029): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0034 | 0/0 | 10033 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0036 | 0/0 | 10036 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0037 | 0/0 | 10037 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0038 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0041 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0042 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0043 | 0/0 | 10037 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0044 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0046 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0049 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0050 | 0/0 | 10036 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0051 | 0/0 | 10036 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0052 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0053 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0056 | 0/0 | 10038 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0057 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0058 | 0/0 | 10037 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0001t0062 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0002 | 0/0 | 10037 | 11 | 0 | 1 | 10 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0004 | 0/0 | 10033 | 23 | 0 | 0 | 22 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0008 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0017 | 0/0 | 10034 | 3 | 0 | 0 | 2 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10029): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0035 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0040 | 0/0 | 10037 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0045 | 0/0 | 10023 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10018): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0047 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0048 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0002t0054 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0001c0003t0003 | 0/0 | 10036 | 8 | 6 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0004t0016 | 0/0 | 10038 | 3 | 1 | 0 | 1 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0004t0029 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0004t0039 | 0/0 | 10038 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0004t0059 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0007t0005 | 0/0 | 10038 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0001c0008t0001 | 0/0 | 10036 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0009t0026 | 0/0 | 10035 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10030): Show |
chr11 | 44090678 | 44256962 |
a0001c0013t0001 | 0/0 | 10036 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0001c0014t0061 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0002c0005t0019 | 0/0 | 10037 | 3 | 3 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0002c0005t0060 | 0/0 | 10034 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10029): Show |
chr11 | 44090678 | 44256962 |
a0003c0006t0003 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
a0003c0006t0007 | 0/0 | 10037 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0003c0006t0055 | 0/0 | 10038 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10033): Show |
chr11 | 44090678 | 44256962 |
a0004c0012t0002 | 0/0 | 10037 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10032): Show |
chr11 | 44090678 | 44256962 |
a0005c0011t0008 | 0/0 | 10033 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10028): Show |
chr11 | 44090678 | 44256962 |
a0006c0010t0011 | 0/0 | 10036 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | AGACG others(10031): Show |
chr11 | 44090678 | 44256962 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0008g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0010g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0012g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0012g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0014g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0014g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0018g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0018g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0018g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0020g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0021g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0021g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0022g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0022g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0023g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0023g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0024g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0024g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0025g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0025g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0027g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0027g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0028g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0030g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0031g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0032g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0033g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0034g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0036g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0037g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0038g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0041g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0042g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0043g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0044g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0046g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0049g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0050g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0051g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0052g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0053g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0056g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0057g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0058g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0001t0062g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0017g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0017g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0035g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0040g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0045g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0047g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0048g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0002t0054g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0016g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0029g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0039g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0004t0059g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0007t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0007t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0007t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0008t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0009t0026g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0009t0026g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0013t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0001c0014t0061g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0002c0005t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0002c0005t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0002c0005t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0002c0005t0060g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0003c0006t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0003c0006t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0003c0006t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0003c0006t0055g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0004c0012t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0005c0011t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
a0006c0010t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00099 | hp2 | a0001 | c0001 | t0056 | g0067 | EUR | GBR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0324 | EUR | FIN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0253 | EUR | FIN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00438 | hp2 | a0001 | c0008 | t0001 | g0162 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0262 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0057 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00621 | hp2 | a0001 | c0002 | t0047 | g0050 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00639 | hp2 | a0001 | c0001 | t0018 | g0312 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00673 | hp2 | a0001 | c0002 | t0048 | g0028 | EAS | CHS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00735 | hp1 | a0001 | c0001 | t0021 | g0061 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00738 | hp2 | a0001 | c0001 | t0010 | g0058 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG00741 | hp2 | a0001 | c0001 | t0021 | g0060 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01099 | hp2 | a0001 | c0001 | t0036 | g0166 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01109 | hp1 | a0001 | c0003 | t0003 | g0271 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0194 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0323 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01168 | hp2 | a0001 | c0001 | t0013 | g0084 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0066 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01243 | hp1 | a0001 | c0001 | t0020 | g0242 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01261 | hp1 | a0001 | c0001 | t0014 | g0081 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01346 | hp1 | a0001 | c0001 | t0025 | g0018 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01361 | hp1 | a0001 | c0001 | t0043 | g0191 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01496 | hp1 | a0001 | c0003 | t0003 | g0258 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01516 | hp1 | a0001 | c0001 | t0025 | g0083 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0064 | EUR | IBS | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01884 | hp1 | a0001 | c0001 | t0022 | g0327 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0269 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01891 | hp2 | a0002 | c0005 | t0019 | g0237 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01978 | hp1 | a0001 | c0001 | t0007 | g0322 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01978 | hp2 | a0001 | c0001 | t0012 | g0107 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01993 | hp1 | a0001 | c0001 | t0012 | g0108 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02027 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02056 | hp1 | a0001 | c0002 | t0054 | g0016 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02056 | hp2 | a0001 | c0001 | t0012 | g0161 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02074 | hp1 | a0001 | c0002 | t0035 | g0047 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02080 | hp2 | a0001 | c0002 | t0004 | g0048 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02083 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02135 | hp2 | a0001 | c0008 | t0001 | g0163 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0310 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02155 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0223 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0313 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02258 | hp1 | a0003 | c0006 | t0003 | g0317 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02300 | hp1 | a0001 | c0001 | t0012 | g0090 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0068 | AMR | PEL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02523 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | KHV | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0219 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0007 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02615 | hp2 | a0001 | c0001 | t0053 | g0256 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0195 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02622 | hp2 | a0001 | c0001 | t0062 | g0285 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02630 | hp2 | a0001 | c0001 | t0027 | g0283 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02647 | hp2 | a0001 | c0001 | t0018 | g0314 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0006 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02738 | hp1 | a0001 | c0001 | t0050 | g0103 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0308 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0131 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0306 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02818 | hp2 | a0001 | c0007 | t0005 | g0147 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02886 | hp1 | a0001 | c0001 | t0038 | g0071 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02886 | hp2 | a0003 | c0006 | t0007 | g0316 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02896 | hp1 | a0001 | c0009 | t0026 | g0304 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0319 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02922 | hp1 | a0001 | c0001 | t0028 | g0329 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02965 | hp2 | a0001 | c0003 | t0003 | g0259 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02970 | hp1 | a0001 | c0003 | t0003 | g0272 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02970 | hp2 | a0001 | c0009 | t0026 | g0305 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02976 | hp1 | a0001 | c0004 | t0016 | g0177 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03017 | hp1 | a0001 | c0001 | t0037 | g0212 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03017 | hp2 | a0001 | c0004 | t0016 | g0172 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03041 | hp1 | a0001 | c0001 | t0022 | g0328 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0309 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03130 | hp2 | a0001 | c0003 | t0003 | g0273 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03139 | hp1 | a0001 | c0001 | t0052 | g0252 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03139 | hp2 | a0003 | c0006 | t0007 | g0315 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03195 | hp1 | a0001 | c0001 | t0057 | g0171 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0270 | AFR | ESN | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0298 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0170 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0059 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03453 | hp2 | a0002 | c0005 | t0019 | g0236 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03486 | hp1 | a0004 | c0012 | t0002 | g0186 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03486 | hp2 | a0001 | c0014 | t0061 | g0238 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03540 | hp1 | a0001 | c0001 | t0027 | g0284 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03540 | hp2 | a0001 | c0001 | t0015 | g0222 | AFR | GWD | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03579 | hp1 | a0003 | c0006 | t0055 | g0318 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03831 | hp1 | a0001 | c0002 | t0017 | g0051 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0137 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0031 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0277 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04115 | hp2 | a0001 | c0001 | t0058 | g0130 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0011 | SAS | BEB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04199 | hp2 | a0001 | c0013 | t0001 | g0087 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04204 | hp2 | a0001 | c0001 | t0034 | g0248 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | STU | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18522 | hp1 | a0002 | c0005 | t0019 | g0239 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18522 | hp2 | a0001 | c0001 | t0020 | g0241 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18906 | hp2 | a0001 | c0007 | t0005 | g0232 | AFR | YRI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18941 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18942 | hp2 | a0001 | c0002 | t0040 | g0025 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18945 | hp1 | a0001 | c0001 | t0008 | g0246 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18945 | hp2 | a0001 | c0001 | t0009 | g0267 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18949 | hp1 | a0001 | c0002 | t0017 | g0046 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18953 | hp1 | a0001 | c0001 | t0023 | g0254 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18954 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18960 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18960 | hp2 | a0001 | c0001 | t0009 | g0282 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18962 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0117 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18969 | hp2 | a0001 | c0002 | t0004 | g0052 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18971 | hp1 | a0005 | c0011 | t0008 | g0250 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0245 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18973 | hp1 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18973 | hp2 | a0001 | c0001 | t0024 | g0143 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18974 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18977 | hp2 | a0001 | c0001 | t0049 | g0094 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18979 | hp1 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18981 | hp1 | a0001 | c0004 | t0016 | g0173 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0260 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18982 | hp2 | a0001 | c0001 | t0051 | g0148 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18986 | hp1 | a0001 | c0004 | t0039 | g0174 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18986 | hp2 | a0001 | c0001 | t0033 | g0216 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18987 | hp2 | a0001 | c0002 | t0017 | g0034 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18990 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18992 | hp1 | a0001 | c0001 | t0009 | g0278 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18992 | hp2 | a0001 | c0001 | t0008 | g0249 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18993 | hp1 | a0001 | c0002 | t0045 | g0056 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA18999 | hp2 | a0001 | c0001 | t0032 | g0202 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19000 | hp1 | a0001 | c0001 | t0009 | g0280 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19001 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19004 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19005 | hp2 | a0001 | c0001 | t0009 | g0264 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19057 | hp1 | a0001 | c0001 | t0042 | g0279 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19065 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19066 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19070 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0244 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19074 | hp2 | a0001 | c0001 | t0009 | g0266 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19075 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19077 | hp1 | a0001 | c0001 | t0009 | g0288 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19079 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19081 | hp1 | a0001 | c0001 | t0041 | g0261 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19082 | hp1 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19083 | hp1 | a0001 | c0001 | t0031 | g0217 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19083 | hp2 | a0001 | c0001 | t0044 | g0299 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19084 | hp2 | a0001 | c0001 | t0023 | g0255 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19088 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19088 | hp2 | a0001 | c0001 | t0024 | g0144 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA19090 | hp2 | a0001 | c0002 | t0008 | g0054 | EAS | JPT | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | ASW | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ASW | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20752 | hp1 | a0001 | c0001 | t0030 | g0287 | EUR | TSI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | TSI | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0325 | SAS | GIH | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | GIH | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG01123 | hp2 | a0001 | c0001 | t0013 | g0008 | AMR | CLM | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0263 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02559 | hp1 | a0002 | c0005 | t0060 | g0240 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03471 | hp1 | a0001 | c0001 | t0046 | g0311 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0276 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
HG06807 | hp2 | a0001 | c0004 | t0059 | g0286 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20300 | hp1 | a0001 | c0007 | t0005 | g0221 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA20300 | hp2 | a0006 | c0010 | t0011 | g0307 | AFR | USA | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
NA21309 | hp2 | a0001 | c0004 | t0029 | g0063 | AFR | LWK | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0183 | REF | REF | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0207 | REF | REF | EXT2_chr11_44090678_44256962 | EXT2 | chr11 | 44090678 | 44256962 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44107836 | A | G | 1 | a0003 | 4 | HG02258.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.124A>G | p.Met42Val | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 329/10037 | 124/2157 | 42/718 | chr11 | 44107836 | |||
chr11:44108124 | T | G | 1 | a0006 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.412T>G | p.Ser138Ala | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 617/10037 | 412/2157 | 138/718 | chr11 | 44108124 | |||
chr11:44124877 | G | A | 1 | a0005 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.832G>A | p.Glu278Lys | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/14 | 1037/10037 | 832/2157 | 278/718 | chr11 | 44124877 | |||
chr11:44130075 | G | T | 1 | a0002 | 4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1110G>T | p.Met370Ile | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/14 | 1315/10037 | 1110/2157 | 370/718 | chr11 | 44130075 | |||
chr11:44206916 | A | T | 1 | a0004 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1619A>T | p.Asp540Val | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/14 | 1824/10037 | 1619/2157 | 540/718 | chr11 | 44206916 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44107740 | C | A | 1 | a0001c0002 | 44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
synonymous_variant | LOW | c.28C>A | p.Arg10Arg | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 233/10037 | 28/2157 | 10/718 | chr11 | 44107740 | |||
chr11:44107976 | C | T | 3 | a0001c0009 a0001c0014 a0002c0005 |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.264C>T | p.His88His | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/14 | 469/10037 | 264/2157 | 88/718 | chr11 | 44107976 | |||
chr11:44124963 | C | T | 1 | a0001c0009 | 2 | HG02896.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.918C>T | p.Phe306Phe | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/14 | 1123/10037 | 918/2157 | 306/718 | chr11 | 44124963 | |||
chr11:44126875 | T | C | 1 | a0001c0004 | 6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
synonymous_variant | LOW | c.999T>C | p.Asp333Asp | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/14 | 1204/10037 | 999/2157 | 333/718 | chr11 | 44126875 | |||
chr11:44126893 | T | C | 1 | a0001c0007 | 3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1017T>C | p.Cys339Cys | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/14 | 1222/10037 | 1017/2157 | 339/718 | chr11 | 44126893 | |||
chr11:44197840 | C | T | 1 | a0001c0013 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1317C>T | p.Ser439Ser | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/14 | 1522/10037 | 1317/2157 | 439/718 | chr11 | 44197840 | |||
chr11:44206938 | C | T | 1 | a0001c0008 | 2 | HG00438.hp2 HG02135.hp2 |
synonymous_variant | LOW | c.1641C>T | p.Asp547Asp | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/14 | 1846/10037 | 1641/2157 | 547/718 | chr11 | 44206938 | |||
chr11:44232451 | G | A | 1 | a0001c0003 | 8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.1761G>A | p.Thr587Thr | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/14 | 1966/10037 | 1761/2157 | 587/718 | chr11 | 44232451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44095686 | C | G | 6 | a0001c0001t0027 a0001c0001t0062 a0001c0009t0026 others(3): Show |
10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-197C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 12027 | chr11 | 44095686 | ||||||
chr11:44095731 | C | G | 1 | a0001c0004t0059 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-152C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 11982 | chr11 | 44095731 | ||||||
chr11:44095735 | G | A | 1 | a0001c0001t0028 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | 11978 | chr11 | 44095735 | ||||||
chr11:44095822 | C | G | 1 | a0001c0001t0058 | 1 | HG04115.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/14 | chr11 | 44095822 | |||||||
chr11:44244297 | T | C | 1 | a0001c0004t0029 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 10 | chr11 | 44244297 | ||||||
chr11:44244343 | G | A | 9 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0031 others(6): Show |
18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 56 | chr11 | 44244343 | ||||||
chr11:44244388 | G | C | 1 | a0001c0001t0036 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 101 | chr11 | 44244388 | ||||||
chr11:44244759 | C | T | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*472C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 472 | chr11 | 44244759 | ||||||
chr11:44245082 | C | A | 1 | a0001c0009t0026 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*795C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 795 | chr11 | 44245082 | ||||||
chr11:44245158 | G | A | 1 | a0001c0001t0037 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 871 | chr11 | 44245158 | ||||||
chr11:44245456 | C | A | 1 | a0001c0001t0038 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1169 | chr11 | 44245456 | ||||||
chr11:44245484 | G | A | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1197 | chr11 | 44245484 | ||||||
chr11:44245506 | G | A | 8 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0031 others(5): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1219G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1219 | chr11 | 44245506 | ||||||
chr11:44245549 | T | G | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1262T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1262 | chr11 | 44245549 | ||||||
chr11:44245760 | C | G | 1 | a0001c0001t0012 | 5 | HG01978.hp2 HG01993.hp1 HG02056.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1473C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1473 | chr11 | 44245760 | ||||||
chr11:44245786 | T | G | 9 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0021 others(6): Show |
54 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1499T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1499 | chr11 | 44245786 | ||||||
chr11:44246011 | T | G | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1724T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1724 | chr11 | 44246011 | ||||||
chr11:44246079 | G | A | 1 | a0001c0001t0022 | 2 | HG01884.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1792G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1792 | chr11 | 44246079 | ||||||
chr11:44246107 | A | G | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
243 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*1820A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1820 | chr11 | 44246107 | ||||||
chr11:44246254 | T | G | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1967T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1967 | chr11 | 44246254 | ||||||
chr11:44246278 | T | C | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 1991 | chr11 | 44246278 | ||||||
chr11:44246322 | G | A | 1 | a0001c0002t0047 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2035 | chr11 | 44246322 | ||||||
chr11:44246511 | G | A | 1 | a0001c0001t0041 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2224G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2224 | chr11 | 44246511 | ||||||
chr11:44246729 | A | C | 1 | a0002c0005t0019 | 3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2442A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2442 | chr11 | 44246729 | ||||||
chr11:44246750 | T | A | 1 | a0001c0002t0048 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2463 | chr11 | 44246750 | ||||||
chr11:44246764 | A | G | 12 | a0001c0001t0008 a0001c0001t0018 a0001c0001t0027 others(9): Show |
24 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2477A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2477 | chr11 | 44246764 | ||||||
chr11:44246805 | GGTCAGGA others(6): Show |
G | 1 | a0001c0002t0045 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2522_*2534delAGGA others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2522 | INFO_REALIGN_3_PRIME | chr11 | 44246805 | |||||
chr11:44246948 | C | T | 1 | a0001c0001t0034 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2661C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2661 | chr11 | 44246948 | ||||||
chr11:44246965 | C | T | 1 | a0002c0005t0060 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2678C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2678 | chr11 | 44246965 | ||||||
chr11:44247154 | C | A | 1 | a0001c0001t0049 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2867C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2867 | chr11 | 44247154 | ||||||
chr11:44247243 | C | CT | 32 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(29): Show |
130 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2976dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2977 | INFO_REALIGN_3_PRIME | chr11 | 44247243 | |||||
chr11:44247243 | C | CTT | 8 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0028 others(5): Show |
33 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2975_*2976dupTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 2977 | INFO_REALIGN_3_PRIME | chr11 | 44247243 | |||||
chr11:44247300 | GCAA | G | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*3017_*3019delCAA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3017 | INFO_REALIGN_3_PRIME | chr11 | 44247300 | |||||
chr11:44247441 | A | AG | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
300 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*3157dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3158 | INFO_REALIGN_3_PRIME | chr11 | 44247441 | |||||
chr11:44247471 | C | G | 1 | a0001c0001t0051 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3184C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3184 | chr11 | 44247471 | ||||||
chr11:44247482 | C | T | 2 | a0001c0001t0062 a0002c0005t0060 |
2 | HG02559.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3195C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3195 | chr11 | 44247482 | ||||||
chr11:44247501 | C | T | 5 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0022 others(2): Show |
13 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3214C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3214 | chr11 | 44247501 | ||||||
chr11:44247528 | G | A | 1 | a0001c0001t0050 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3241G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3241 | chr11 | 44247528 | ||||||
chr11:44247716 | G | A | 1 | a0001c0001t0043 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3429G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3429 | chr11 | 44247716 | ||||||
chr11:44247851 | G | A | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*3564G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3564 | chr11 | 44247851 | ||||||
chr11:44247869 | T | C | 1 | a0001c0001t0020 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3582T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3582 | chr11 | 44247869 | ||||||
chr11:44247930 | T | C | 2 | a0001c0001t0052 a0001c0014t0061 |
2 | HG03139.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3643 | chr11 | 44247930 | ||||||
chr11:44247946 | T | C | 1 | a0001c0001t0030 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3659T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3659 | chr11 | 44247946 | ||||||
chr11:44247946 | T | G | 1 | a0001c0001t0024 | 2 | NA18973.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3659T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3659 | chr11 | 44247946 | ||||||
chr11:44247991 | G | A | 1 | a0001c0001t0042 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3704G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 3704 | chr11 | 44247991 | ||||||
chr11:44248512 | C | G | 1 | a0001c0001t0018 | 3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4225C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4225 | chr11 | 44248512 | ||||||
chr11:44248964 | G | GT | 8 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0025 others(5): Show |
17 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4684dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4685 | INFO_REALIGN_3_PRIME | chr11 | 44248964 | |||||
chr11:44248964 | GT | G | 9 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0031 others(6): Show |
18 | HG02559.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4684delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4684 | INFO_REALIGN_3_PRIME | chr11 | 44248964 | |||||
chr11:44248968 | TTTTG | T | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4701_*4704delGTTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4701 | INFO_REALIGN_3_PRIME | chr11 | 44248968 | |||||
chr11:44248972 | G | T | 3 | a0001c0001t0010 a0001c0001t0021 a0003c0006t0055 |
7 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4685G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4685 | chr11 | 44248972 | ||||||
chr11:44249051 | T | C | 1 | a0001c0009t0026 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4764T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4764 | chr11 | 44249051 | ||||||
chr11:44249070 | C | T | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4783C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4783 | chr11 | 44249070 | ||||||
chr11:44249093 | C | T | 1 | a0001c0001t0025 | 2 | HG01346.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4806C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4806 | chr11 | 44249093 | ||||||
chr11:44249125 | T | A | 1 | a0001c0001t0057 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4838T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 4838 | chr11 | 44249125 | ||||||
chr11:44249329 | CAGTT | C | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(3): Show |
31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5043_*5046delAGTT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5043 | chr11 | 44249329 | ||||||
chr11:44249413 | A | G | 6 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(3): Show |
31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5126A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5126 | chr11 | 44249413 | ||||||
chr11:44249443 | G | T | 1 | a0001c0001t0032 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5156G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5156 | chr11 | 44249443 | ||||||
chr11:44249451 | A | C | 1 | a0001c0009t0026 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5164A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5164 | chr11 | 44249451 | ||||||
chr11:44249611 | T | C | 1 | a0001c0001t0056 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5324T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5324 | chr11 | 44249611 | ||||||
chr11:44249623 | T | G | 1 | a0001c0004t0059 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5336 | chr11 | 44249623 | ||||||
chr11:44250024 | T | C | 1 | a0001c0009t0026 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5737T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5737 | chr11 | 44250024 | ||||||
chr11:44250115 | A | G | 1 | a0001c0001t0031 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5828A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5828 | chr11 | 44250115 | ||||||
chr11:44250116 | G | C | 1 | a0001c0001t0031 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 5829 | chr11 | 44250116 | ||||||
chr11:44250523 | C | T | 10 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(7): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6236C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6236 | chr11 | 44250523 | ||||||
chr11:44250529 | A | G | 1 | a0001c0001t0052 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6242A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6242 | chr11 | 44250529 | ||||||
chr11:44250600 | C | A | 1 | a0001c0002t0054 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6313C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6313 | chr11 | 44250600 | ||||||
chr11:44250724 | G | A | 1 | a0001c0001t0028 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6437G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6437 | chr11 | 44250724 | ||||||
chr11:44250823 | T | G | 1 | a0001c0001t0049 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6536T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6536 | chr11 | 44250823 | ||||||
chr11:44250972 | A | G | 10 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0021 others(7): Show |
55 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*6685A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6685 | chr11 | 44250972 | ||||||
chr11:44251194 | T | TC | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
295 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*6908dupC | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 6909 | INFO_REALIGN_3_PRIME | chr11 | 44251194 | |||||
chr11:44251408 | G | A | 1 | a0003c0006t0055 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7121G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7121 | chr11 | 44251408 | ||||||
chr11:44251411 | T | C | 1 | a0001c0001t0053 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7124T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7124 | chr11 | 44251411 | ||||||
chr11:44251516 | G | A | 1 | a0001c0009t0026 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7229G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7229 | chr11 | 44251516 | ||||||
chr11:44251593 | A | G | 1 | a0001c0001t0023 | 2 | NA18953.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7306A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7306 | chr11 | 44251593 | ||||||
chr11:44251874 | C | T | 6 | a0001c0001t0010 a0001c0001t0025 a0001c0004t0016 others(3): Show |
14 | HG00738.hp2 HG01109.hp2 HG01346.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7587C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7587 | chr11 | 44251874 | ||||||
chr11:44251892 | A | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
290 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*7605A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7605 | chr11 | 44251892 | ||||||
chr11:44251935 | T | C | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7648T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7648 | chr11 | 44251935 | ||||||
chr11:44251936 | G | A | 5 | a0001c0001t0009 a0001c0001t0023 a0001c0001t0041 others(2): Show |
17 | HG00544.hp2 HG02523.hp2 NA18945.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*7649G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 14/14 | 7649 | chr11 | 44251936 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:44095859 | G | T | 15 | a0001c0001t0001g0326 a0001c0001t0004g0325 a0001c0001t0007g0319 others(12): Show |
15 | HG00323.hp1 HG01168.hp1 HG01884.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-31+7G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095859 | |||||||
chr11:44095874 | G | A | 171 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-31+22G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095874 | |||||||
chr11:44095894 | A | G | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.-31+42A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095894 | |||||||
chr11:44095958 | C | T | 7 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(4): Show |
7 | HG02723.hp1 HG03017.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+106C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44095958 | |||||||
chr11:44096217 | C | T | 1 | a0001c0002t0002g0026 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-31+365C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096217 | |||||||
chr11:44096326 | G | A | 3 | a0001c0001t0013g0006 a0001c0001t0013g0007 a0001c0001t0013g0008 |
3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-31+474G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096326 | |||||||
chr11:44096348 | T | G | 259 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-31+496T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096348 | |||||||
chr11:44096365 | TCGGGGGC others(39): Show |
T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-31+543_-31+588del others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44096365 | ||||||
chr11:44096509 | G | A | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+657G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096509 | |||||||
chr11:44096817 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+965G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44096817 | |||||||
chr11:44097086 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG04184.hp2 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+1234G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097086 | |||||||
chr11:44097104 | G | A | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+1252G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097104 | |||||||
chr11:44097131 | T | C | 6 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(3): Show |
6 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+1279T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097131 | |||||||
chr11:44097201 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31+1349A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097201 | |||||||
chr11:44097213 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-31+1361A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097213 | |||||||
chr11:44097301 | T | C | 10 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+1449T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097301 | |||||||
chr11:44097380 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-31+1528A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097380 | |||||||
chr11:44097443 | A | G | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-31+1591A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097443 | |||||||
chr11:44097515 | C | T | 10 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+1663C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097515 | |||||||
chr11:44097517 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+1665C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097517 | |||||||
chr11:44097528 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-31+1676G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097528 | |||||||
chr11:44097578 | C | T | 15 | a0001c0001t0003g0289 a0001c0001t0003g0290 a0001c0001t0003g0291 others(12): Show |
15 | HG02027.hp2 HG02135.hp1 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+1726C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097578 | |||||||
chr11:44097761 | AAAAT | A | 15 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(12): Show |
15 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+1945_-31+1948d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097761 | ||||||
chr11:44097761 | AAAATAAA others(1): Show |
A | 146 | a0001c0001t0001g0085 a0001c0001t0001g0178 a0001c0001t0001g0275 others(143): Show |
149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-31+1941_-31+1948d others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097761 | ||||||
chr11:44097762 | AAATAAAT | A | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(119): Show |
123 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-31+1913_-31+1919d others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097762 | ||||||
chr11:44097763 | AATAAATA others(3): Show |
A | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+1913_-31+1922d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44097763 | ||||||
chr11:44097764 | ATAAATAA others(2): Show |
A | 12 | a0001c0001t0003g0302 a0001c0001t0008g0003 a0001c0001t0008g0243 others(9): Show |
13 | HG02896.hp2 HG04204.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+1913_-31+1921d others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097764 | |||||||
chr11:44097773 | T | A | 154 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(151): Show |
156 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-31+1921T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097773 | |||||||
chr11:44097777 | T | A | 149 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(146): Show |
152 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-31+1925T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097777 | |||||||
chr11:44097781 | T | A | 19 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0002g0089 others(16): Show |
20 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+1929T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097781 | |||||||
chr11:44097957 | G | A | 1 | a0001c0001t0012g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-31+2105G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44097957 | |||||||
chr11:44098220 | C | T | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-31+2368C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098220 | |||||||
chr11:44098221 | G | A | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+2369G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098221 | |||||||
chr11:44098254 | G | A | 1 | a0001c0001t0006g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-31+2402G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098254 | |||||||
chr11:44098477 | G | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+2625G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098477 | |||||||
chr11:44098626 | C | G | 10 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+2774C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098626 | |||||||
chr11:44098694 | C | CA | 35 | a0001c0001t0001g0010 a0001c0001t0001g0326 a0001c0001t0002g0192 others(32): Show |
36 | HG00323.hp1 HG01099.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-31+2860dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44098694 | ||||||
chr11:44098694 | CA | C | 38 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0003g0274 others(35): Show |
40 | HG00544.hp2 HG01109.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-31+2860delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44098694 | ||||||
chr11:44098699 | A | C | 1 | a0001c0001t0001g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+2847A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44098699 | |||||||
chr11:44099063 | G | A | 53 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(50): Show |
55 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-31+3211G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099063 | |||||||
chr11:44099074 | T | G | 50 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(47): Show |
51 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-31+3222T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099074 | |||||||
chr11:44099141 | G | A | 1 | a0001c0001t0006g0092 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-31+3289G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099141 | |||||||
chr11:44099176 | G | GT | 7 | a0001c0001t0002g0233 a0001c0001t0006g0157 a0001c0001t0006g0158 others(4): Show |
7 | HG00597.hp2 HG03834.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+3333dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44099176 | ||||||
chr11:44099177 | T | G | 9 | a0001c0001t0001g0093 a0001c0001t0010g0058 a0001c0001t0010g0059 others(6): Show |
9 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+3325T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099177 | |||||||
chr11:44099256 | G | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+3404G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099256 | |||||||
chr11:44099451 | C | T | 50 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(47): Show |
51 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-31+3599C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099451 | |||||||
chr11:44099518 | C | T | 116 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(113): Show |
117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-31+3666C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099518 | |||||||
chr11:44099890 | C | A | 2 | a0001c0001t0023g0254 a0001c0001t0023g0255 |
2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-31+4038C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099890 | |||||||
chr11:44099957 | G | A | 2 | a0001c0001t0052g0252 a0001c0001t0053g0256 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-31+4105G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099957 | |||||||
chr11:44099963 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+4111A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44099963 | |||||||
chr11:44100152 | A | G | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-31+4300A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100152 | |||||||
chr11:44100186 | A | T | 79 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(76): Show |
80 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-31+4334A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100186 | |||||||
chr11:44100525 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-31+4673G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100525 | |||||||
chr11:44100533 | G | T | 168 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0002g0251 others(165): Show |
172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.-31+4681G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44100533 | |||||||
chr11:44101005 | C | T | 29 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(26): Show |
29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-31+5153C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101005 | |||||||
chr11:44101070 | A | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-31+5218A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101070 | |||||||
chr11:44101129 | T | G | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-31+5277T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101129 | |||||||
chr11:44101151 | G | C | 1 | a0001c0002t0004g0020 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-31+5299G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101151 | |||||||
chr11:44101277 | G | A | 47 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0003g0274 others(44): Show |
49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-31+5425G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101277 | |||||||
chr11:44101300 | C | T | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-31+5448C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101300 | |||||||
chr11:44101442 | A | G | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-31+5590A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101442 | |||||||
chr11:44101446 | A | G | 6 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(3): Show |
6 | HG02559.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5594A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101446 | |||||||
chr11:44101534 | G | A | 2 | a0001c0001t0003g0297 a0001c0001t0003g0302 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+5682G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101534 | |||||||
chr11:44101694 | G | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31+5842G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101694 | |||||||
chr11:44101936 | A | G | 1 | a0001c0001t0022g0328 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-30-5747A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101936 | |||||||
chr11:44101944 | T | TA | 114 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(111): Show |
116 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-30-5718dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | ||||||
chr11:44101944 | T | TAA | 19 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
19 | HG00621.hp1 HG00735.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30-5719_-30-5718d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | ||||||
chr11:44101944 | TA | T | 96 | a0001c0001t0001g0218 a0001c0001t0003g0296 a0001c0001t0003g0301 others(93): Show |
97 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-30-5718delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44101944 | ||||||
chr11:44101953 | A | G | 78 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(75): Show |
79 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-30-5730A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101953 | |||||||
chr11:44101954 | A | G | 1 | a0001c0002t0002g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-30-5729A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101954 | |||||||
chr11:44101961 | A | G | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-30-5722A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44101961 | |||||||
chr11:44102029 | C | T | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-30-5654C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102029 | |||||||
chr11:44102065 | T | C | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-5618T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102065 | |||||||
chr11:44102100 | C | T | 1 | a0001c0001t0006g0092 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-30-5583C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102100 | |||||||
chr11:44102174 | T | C | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-30-5509T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102174 | |||||||
chr11:44102413 | G | T | 1 | a0001c0007t0005g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-30-5270G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102413 | |||||||
chr11:44102534 | C | CT | 12 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
12 | HG00597.hp1 HG01361.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-5128dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | ||||||
chr11:44102534 | CT | C | 92 | a0001c0001t0001g0093 a0001c0001t0001g0159 a0001c0001t0001g0275 others(89): Show |
95 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-30-5128delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | ||||||
chr11:44102534 | CTT | C | 88 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(85): Show |
89 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-30-5129_-30-5128d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 44102534 | ||||||
chr11:44102537 | T | C | 1 | a0001c0001t0008g0003 | 2 | NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-30-5146T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102537 | |||||||
chr11:44102565 | C | T | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-5118C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102565 | |||||||
chr11:44102616 | C | G | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-5067C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102616 | |||||||
chr11:44102628 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-30-5055A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102628 | |||||||
chr11:44102768 | T | C | 83 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(80): Show |
84 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-30-4915T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44102768 | |||||||
chr11:44103177 | G | A | 4 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-4506G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103177 | |||||||
chr11:44103319 | G | T | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-4364G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103319 | |||||||
chr11:44103442 | A | G | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-4241A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103442 | |||||||
chr11:44103799 | G | A | 47 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0003g0274 others(44): Show |
49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30-3884G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103799 | |||||||
chr11:44103990 | C | T | 169 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0002g0251 others(166): Show |
173 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-30-3693C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44103990 | |||||||
chr11:44104147 | G | A | 2 | a0001c0001t0025g0018 a0001c0001t0025g0083 |
2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-30-3536G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104147 | |||||||
chr11:44104690 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-30-2993C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104690 | |||||||
chr11:44104780 | T | C | 75 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0003g0268 others(72): Show |
77 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-30-2903T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104780 | |||||||
chr11:44104836 | G | A | 1 | a0001c0002t0004g0022 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-30-2847G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104836 | |||||||
chr11:44104955 | G | A | 1 | a0001c0001t0011g0308 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30-2728G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44104955 | |||||||
chr11:44105229 | A | G | 1 | a0001c0004t0039g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-30-2454A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105229 | |||||||
chr11:44105262 | G | A | 4 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(1): Show |
4 | HG02723.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-2421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105262 | |||||||
chr11:44105334 | C | T | 79 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(76): Show |
80 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-30-2349C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105334 | |||||||
chr11:44105438 | T | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0050g0103 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-30-2245T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105438 | |||||||
chr11:44105555 | G | C | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-2128G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105555 | |||||||
chr11:44105743 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-1940G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105743 | |||||||
chr11:44105760 | T | C | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-1923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44105760 | |||||||
chr11:44106011 | C | T | 1 | a0001c0001t0057g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30-1672C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106011 | |||||||
chr11:44106273 | A | G | 63 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0003g0268 others(60): Show |
65 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-30-1410A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106273 | |||||||
chr11:44106369 | T | A | 1 | a0001c0001t0012g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-30-1314T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106369 | |||||||
chr11:44106425 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-30-1258T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106425 | |||||||
chr11:44106495 | T | A | 96 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(93): Show |
96 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-30-1188T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106495 | |||||||
chr11:44106501 | T | C | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-1182T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106501 | |||||||
chr11:44106559 | C | A | 1 | a0001c0001t0005g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-30-1124C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106559 | |||||||
chr11:44106742 | G | C | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-941G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106742 | |||||||
chr11:44106777 | A | C | 7 | a0001c0001t0001g0176 a0001c0001t0010g0002 a0001c0001t0010g0194 others(4): Show |
8 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-906A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106777 | |||||||
chr11:44106793 | C | G | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-890C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44106793 | |||||||
chr11:44107140 | A | G | 47 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0003g0274 others(44): Show |
49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30-543A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107140 | |||||||
chr11:44107245 | G | A | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-30-438G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107245 | |||||||
chr11:44107269 | C | T | 1 | a0002c0005t0019g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-30-414C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107269 | |||||||
chr11:44107536 | A | T | 83 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(80): Show |
84 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-30-147A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107536 | |||||||
chr11:44107603 | A | C | 18 | a0001c0001t0006g0091 a0001c0001t0006g0092 a0001c0001t0006g0102 others(15): Show |
18 | HG00423.hp2 HG02622.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-80A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 1/13 | chr11 | 44107603 | |||||||
chr11:44108380 | G | C | 75 | a0001c0001t0001g0275 a0001c0001t0001g0326 a0001c0001t0003g0268 others(72): Show |
77 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.536+132G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44108380 | |||||||
chr11:44108429 | G | A | 1 | a0001c0001t0005g0062 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.536+181G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44108429 | |||||||
chr11:44109096 | T | G | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.537-98T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109096 | |||||||
chr11:44109110 | C | T | 1 | a0001c0001t0007g0324 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.537-84C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109110 | |||||||
chr11:44109115 | A | C | 47 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0003g0274 others(44): Show |
49 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.537-79A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 2/13 | chr11 | 44109115 | |||||||
chr11:44109411 | A | T | 2 | a0001c0001t0003g0297 a0001c0001t0003g0302 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.626+128A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109411 | |||||||
chr11:44109422 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.626+139C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109422 | |||||||
chr11:44109545 | C | G | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+262C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109545 | |||||||
chr11:44109587 | G | A | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+304G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109587 | |||||||
chr11:44109623 | G | A | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.626+340G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109623 | |||||||
chr11:44109641 | T | C | 1 | a0001c0001t0002g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.626+358T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109641 | |||||||
chr11:44109674 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.626+391G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109674 | |||||||
chr11:44109804 | C | T | 219 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.626+521C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109804 | |||||||
chr11:44109869 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.626+586A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44109869 | |||||||
chr11:44110014 | G | C | 1 | a0001c0003t0003g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.626+731G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110014 | |||||||
chr11:44110016 | C | T | 1 | a0001c0002t0008g0054 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.626+733C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110016 | |||||||
chr11:44110017 | G | A | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+734G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110017 | |||||||
chr11:44110030 | G | A | 2 | a0001c0001t0012g0107 a0001c0001t0012g0108 |
2 | HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.626+747G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110030 | |||||||
chr11:44110440 | G | A | 1 | a0001c0004t0029g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+1157G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110440 | |||||||
chr11:44110476 | G | A | 4 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+1193G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110476 | |||||||
chr11:44110779 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.626+1496C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44110779 | |||||||
chr11:44111083 | G | A | 7 | a0001c0001t0003g0289 a0001c0001t0003g0290 a0001c0001t0003g0291 others(4): Show |
7 | NA18949.hp2 NA18980.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+1800G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111083 | |||||||
chr11:44111330 | C | T | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.626+2047C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111330 | |||||||
chr11:44111354 | CCT | C | 4 | a0001c0001t0005g0077 a0001c0001t0005g0078 a0001c0001t0005g0079 others(1): Show |
4 | HG00609.hp1 NA18941.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+2074_626+2075d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr11 | 44111354 | ||||||
chr11:44111551 | C | T | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.626+2268C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111551 | |||||||
chr11:44111773 | C | T | 1 | a0001c0001t0034g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.627-2412C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111773 | |||||||
chr11:44111936 | A | G | 3 | a0001c0001t0005g0062 a0001c0001t0005g0076 a0001c0002t0004g0053 |
3 | NA18968.hp2 NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.627-2249A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44111936 | |||||||
chr11:44112033 | G | A | 44 | a0001c0001t0003g0289 a0001c0002t0002g0021 a0001c0002t0002g0023 others(41): Show |
45 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.627-2152G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112033 | |||||||
chr11:44112133 | C | T | 195 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.627-2052C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112133 | |||||||
chr11:44112166 | G | A | 2 | a0001c0007t0005g0221 a0001c0007t0005g0232 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.627-2019G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112166 | |||||||
chr11:44112166 | G | C | 1 | a0003c0006t0003g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.627-2019G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112166 | |||||||
chr11:44112322 | G | A | 16 | a0001c0001t0001g0326 a0001c0001t0004g0325 a0001c0001t0007g0169 others(13): Show |
16 | HG00323.hp1 HG01168.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.627-1863G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112322 | |||||||
chr11:44112591 | G | A | 193 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.627-1594G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112591 | |||||||
chr11:44112749 | C | T | 31 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(28): Show |
31 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.627-1436C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112749 | |||||||
chr11:44112889 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.627-1296C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44112889 | |||||||
chr11:44113057 | C | T | 44 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(41): Show |
45 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.627-1128C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113057 | |||||||
chr11:44113227 | A | G | 7 | a0001c0009t0026g0304 a0001c0009t0026g0305 a0001c0014t0061g0238 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-958A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113227 | |||||||
chr11:44113366 | G | A | 21 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(18): Show |
21 | HG00099.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.627-819G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113366 | |||||||
chr11:44113439 | T | G | 1 | a0001c0001t0018g0312 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.627-746T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113439 | |||||||
chr11:44113663 | G | A | 1 | a0001c0004t0039g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.627-522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113663 | |||||||
chr11:44113869 | G | A | 5 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(2): Show |
5 | NA18943.hp1 NA18947.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-316G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113869 | |||||||
chr11:44113875 | G | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.627-310G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113875 | |||||||
chr11:44113885 | A | T | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-300A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113885 | |||||||
chr11:44113962 | G | C | 1 | a0001c0014t0061g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.627-223G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113962 | |||||||
chr11:44113998 | T | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.627-187T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44113998 | |||||||
chr11:44114117 | C | T | 1 | a0001c0007t0005g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.627-68C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 3/13 | chr11 | 44114117 | |||||||
chr11:44114444 | C | T | 4 | a0001c0001t0013g0006 a0001c0001t0013g0007 a0001c0001t0013g0008 others(1): Show |
4 | HG01123.hp2 HG01168.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+143C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114444 | |||||||
chr11:44114510 | A | C | 1 | a0001c0002t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.743+209A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114510 | |||||||
chr11:44114574 | A | G | 1 | a0001c0001t0037g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.743+273A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114574 | |||||||
chr11:44114657 | C | T | 1 | a0001c0001t0006g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.743+356C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114657 | |||||||
chr11:44114692 | C | T | 1 | a0001c0001t0007g0323 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.743+391C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114692 | |||||||
chr11:44114788 | T | TA | 45 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(42): Show |
46 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.743+488dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44114788 | ||||||
chr11:44114808 | A | G | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.743+507A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44114808 | |||||||
chr11:44115036 | G | A | 2 | a0001c0001t0002g0197 a0001c0001t0002g0198 |
2 | HG00639.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.743+735G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115036 | |||||||
chr11:44115088 | C | G | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.743+787C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115088 | |||||||
chr11:44115095 | G | A | 1 | a0001c0003t0003g0259 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.743+794G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115095 | |||||||
chr11:44115185 | C | T | 53 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0003g0190 others(50): Show |
55 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.743+884C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115185 | |||||||
chr11:44115410 | T | A | 7 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(4): Show |
7 | HG01993.hp2 NA18942.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+1109T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115410 | |||||||
chr11:44115456 | A | G | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+1155A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115456 | |||||||
chr11:44115486 | A | G | 16 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(13): Show |
16 | HG01243.hp1 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.743+1185A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115486 | |||||||
chr11:44115670 | C | A | 269 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.743+1369C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115670 | |||||||
chr11:44115693 | T | G | 51 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(48): Show |
52 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.743+1392T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115693 | |||||||
chr11:44115872 | G | A | 1 | a0001c0001t0027g0283 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.743+1571G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44115872 | |||||||
chr11:44116067 | C | T | 2 | a0001c0001t0052g0252 a0001c0001t0053g0256 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.743+1766C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116067 | |||||||
chr11:44116219 | C | G | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(82): Show |
85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.743+1918C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116219 | |||||||
chr11:44116818 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.743+2517A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116818 | |||||||
chr11:44116899 | G | A | 14 | a0001c0001t0001g0326 a0001c0001t0004g0325 a0001c0001t0007g0169 others(11): Show |
14 | HG00323.hp1 HG01168.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.743+2598G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44116899 | |||||||
chr11:44116969 | C | CT | 7 | a0001c0001t0001g0012 a0001c0001t0002g0180 a0001c0001t0025g0018 others(4): Show |
7 | HG01081.hp2 HG01346.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+2685dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44116969 | ||||||
chr11:44116969 | CT | C | 13 | a0001c0001t0003g0290 a0001c0001t0005g0019 a0001c0001t0008g0003 others(10): Show |
14 | HG01515.hp2 HG01993.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+2685delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44116969 | ||||||
chr11:44117126 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.743+2825C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117126 | |||||||
chr11:44117152 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.743+2851A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117152 | |||||||
chr11:44117451 | C | A | 193 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0001g0326 others(190): Show |
198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.743+3150C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117451 | |||||||
chr11:44117511 | C | A | 5 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0001c0001t0005g0068 others(2): Show |
5 | HG00099.hp2 HG01192.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+3210C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117511 | |||||||
chr11:44117557 | T | C | 1 | a0001c0002t0048g0028 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.743+3256T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117557 | |||||||
chr11:44117653 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.743+3352C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117653 | |||||||
chr11:44117733 | A | C | 11 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(8): Show |
12 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+3432A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117733 | |||||||
chr11:44117809 | T | A | 29 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(26): Show |
29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.743+3508T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117809 | |||||||
chr11:44117908 | C | A | 1 | a0001c0001t0007g0324 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.743+3607C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44117908 | |||||||
chr11:44118121 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.743+3820G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118121 | |||||||
chr11:44118123 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.743+3822A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118123 | |||||||
chr11:44118339 | A | G | 1 | a0001c0004t0029g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.743+4038A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118339 | |||||||
chr11:44118587 | C | G | 10 | a0001c0001t0005g0062 a0001c0001t0005g0072 a0001c0001t0005g0074 others(7): Show |
10 | HG00609.hp1 NA18747.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4286C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118587 | |||||||
chr11:44118743 | G | A | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.743+4442G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118743 | |||||||
chr11:44118837 | G | A | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4536G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118837 | |||||||
chr11:44118841 | G | A | 12 | a0001c0001t0010g0002 a0001c0001t0010g0194 a0001c0001t0010g0195 others(9): Show |
13 | HG01109.hp2 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.743+4540G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118841 | |||||||
chr11:44118844 | A | G | 33 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(30): Show |
33 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.743+4543A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118844 | |||||||
chr11:44118907 | A | G | 10 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.743+4606A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44118907 | |||||||
chr11:44119122 | A | ATT | 6 | a0001c0001t0001g0126 a0001c0001t0001g0155 a0001c0001t0006g0142 others(3): Show |
6 | HG00673.hp1 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+4823_743+4824d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119122 | ||||||
chr11:44119124 | T | A | 1 | a0001c0002t0008g0054 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.743+4823T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | |||||||
chr11:44119124 | T | TA | 3 | a0001c0001t0002g0199 a0001c0002t0004g0029 a0001c0007t0005g0221 |
3 | HG02165.hp1 NA18966.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.743+4823_743+4824i others(3): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | |||||||
chr11:44119124 | T | TATATATA others(6): Show |
1 | a0001c0001t0009g0288 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(15): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | |||||||
chr11:44119124 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(19): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | |||||||
chr11:44119124 | T | TCATATAT others(3): Show |
1 | a0001c0001t0052g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.743+4823_743+4824i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119124 | |||||||
chr11:44119124 | T | TTA | 3 | a0001c0001t0007g0322 a0003c0006t0007g0315 a0003c0006t0007g0316 |
3 | HG01978.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.743+4868_743+4869d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTATA | 4 | a0001c0001t0004g0325 a0001c0001t0007g0175 a0001c0001t0007g0321 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4866_743+4869d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTATATA | 3 | a0001c0001t0001g0326 a0001c0001t0003g0229 a0001c0007t0005g0232 |
3 | NA18906.hp2 NA19001.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743+4864_743+4869d others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTATATAT others(3): Show |
1 | a0001c0001t0057g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.743+4860_743+4869d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTATATAT others(5): Show |
1 | a0001c0001t0007g0320 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.743+4858_743+4869d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTATATAT others(5): Show |
1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+4832_743+4833i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0127 others(8): Show |
11 | HG00099.hp1 HG00735.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+4824_743+4825i others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATA | 3 | a0001c0001t0001g0009 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG00609.hp2 HG02165.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(3): Show |
1 | a0001c0001t0001g0159 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(5): Show |
2 | a0001c0001t0001g0167 a0001c0001t0024g0143 |
2 | NA18950.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(7): Show |
1 | a0001c0001t0018g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(9): Show |
2 | a0001c0001t0018g0312 a0001c0001t0024g0144 |
2 | HG00639.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(11): Show |
1 | a0001c0001t0006g0102 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(19): Show |
1 | a0001c0001t0002g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.743+4824_743+4825i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(21): Show |
2 | a0002c0005t0019g0236 a0002c0005t0019g0239 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+4824_743+4825i others(30): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | T | TTTTATAT others(17): Show |
1 | a0002c0005t0019g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.743+4824_743+4825i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTA | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(19): Show |
22 | HG00423.hp2 HG01123.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.743+4868_743+4869d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATA | T | 14 | a0001c0001t0001g0119 a0001c0001t0003g0220 a0001c0001t0003g0224 others(11): Show |
14 | HG02257.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+4866_743+4869d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(5): Show |
T | 3 | a0001c0001t0010g0194 a0001c0014t0061g0238 a0002c0005t0060g0240 |
3 | HG01109.hp2 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.743+4858_743+4869d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(7): Show |
T | 6 | a0001c0001t0007g0253 a0001c0001t0010g0002 a0001c0001t0010g0195 others(3): Show |
7 | HG00323.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+4856_743+4869d others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(9): Show |
T | 6 | a0001c0001t0011g0308 a0001c0001t0020g0241 a0001c0001t0020g0242 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.743+4854_743+4869d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(11): Show |
T | 2 | a0001c0001t0011g0309 a0001c0001t0011g0310 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.743+4852_743+4869d others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(13): Show |
T | 4 | a0001c0001t0002g0201 a0001c0001t0027g0283 a0001c0001t0027g0284 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4850_743+4869d others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119124 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0042g0279 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.743+4844_743+4869d others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119124 | ||||||
chr11:44119126 | A | T | 80 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0088 others(77): Show |
81 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.743+4825A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119126 | |||||||
chr11:44119128 | A | T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
35 | HG00099.hp2 HG00423.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.743+4827A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119128 | |||||||
chr11:44119130 | A | T | 2 | a0001c0001t0001g0119 a0001c0001t0051g0148 |
2 | NA18982.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.743+4829A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119130 | |||||||
chr11:44119136 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.743+4835A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119136 | |||||||
chr11:44119137 | T | TATAATAT others(32): Show |
1 | a0001c0001t0002g0200 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.743+4839_743+4840i others(41): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | ||||||
chr11:44119137 | T | TATATATA others(7): Show |
1 | a0001c0002t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.743+4849_743+4850i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | ||||||
chr11:44119137 | T | TATATATA others(13): Show |
2 | a0001c0001t0002g0185 a0004c0012t0002g0186 |
2 | HG01515.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.743+4855_743+4856i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | ||||||
chr11:44119137 | T | TATATATA others(19): Show |
1 | a0001c0001t0002g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.743+4861_743+4862i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119137 | ||||||
chr11:44119138 | A | T | 2 | a0001c0014t0061g0238 a0002c0005t0060g0240 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.743+4837A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119138 | |||||||
chr11:44119139 | T | TATATATA others(9): Show |
1 | a0001c0001t0002g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.743+4853_743+4854i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | ||||||
chr11:44119139 | T | TATATATA others(11): Show |
4 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(1): Show |
4 | HG00738.hp1 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4855_743+4856i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | ||||||
chr11:44119139 | T | TATATATA others(15): Show |
2 | a0001c0001t0008g0234 a0001c0001t0033g0216 |
2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.743+4859_743+4860i others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | ||||||
chr11:44119139 | T | TATATATA others(17): Show |
5 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0008g0203 others(2): Show |
5 | NA18999.hp2 NA19004.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+4861_743+4862i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | ||||||
chr11:44119139 | T | TATATATA others(25): Show |
1 | a0001c0001t0002g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.743+4865_743+4866i others(34): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119139 | ||||||
chr11:44119140 | A | T | 1 | a0001c0001t0010g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.743+4839A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119140 | |||||||
chr11:44119143 | T | C | 2 | a0001c0001t0002g0251 a0001c0001t0030g0287 |
2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.743+4842T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119143 | |||||||
chr11:44119145 | T | C | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4844T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119145 | |||||||
chr11:44119151 | T | C | 34 | a0001c0001t0002g0251 a0001c0001t0003g0213 a0001c0001t0005g0019 others(31): Show |
34 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.743+4850T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119151 | |||||||
chr11:44119153 | T | C | 10 | a0001c0001t0005g0075 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+4852T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119153 | |||||||
chr11:44119153 | TATATATA others(11): Show |
T | 32 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(29): Show |
32 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.743+4854_743+4871d others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119153 | ||||||
chr11:44119153 | TATATATA others(17): Show |
T | 2 | a0001c0001t0002g0251 a0001c0001t0030g0287 |
2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.743+4854_743+4877d others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119153 | ||||||
chr11:44119155 | TATATATA others(9): Show |
T | 1 | a0001c0001t0005g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.743+4856_743+4871d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119155 | ||||||
chr11:44119155 | TATATATA others(15): Show |
T | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.743+4856_743+4877d others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119155 | ||||||
chr11:44119163 | TATATATA others(3): Show |
T | 2 | a0001c0001t0006g0164 a0001c0008t0001g0162 |
2 | HG00438.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.743+4866_743+4875d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119163 | ||||||
chr11:44119167 | T | C | 8 | a0001c0001t0007g0253 a0001c0001t0041g0261 a0001c0001t0042g0279 others(5): Show |
8 | HG00323.hp2 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4866T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119167 | |||||||
chr11:44119169 | T | C | 35 | a0001c0001t0001g0176 a0001c0001t0002g0179 a0001c0001t0002g0180 others(32): Show |
35 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.743+4868T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | |||||||
chr11:44119169 | T | G | 33 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(30): Show |
33 | HG00423.hp2 HG01123.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.743+4868T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | |||||||
chr11:44119169 | T | TATACATA others(81): Show |
1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(90): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATACA others(29): Show |
4 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(1): Show |
4 | NA18947.hp1 NA18971.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(38): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(1): Show |
6 | a0001c0001t0003g0190 a0001c0003t0003g0258 a0001c0003t0003g0272 others(3): Show |
6 | HG01496.hp1 HG02970.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(3): Show |
1 | a0001c0002t0045g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(31): Show |
1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(31): Show |
3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0233 |
3 | HG01167.hp2 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(3): Show |
5 | a0001c0001t0003g0230 a0001c0001t0003g0297 a0001c0001t0003g0302 others(2): Show |
5 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(5): Show |
1 | a0001c0002t0004g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(33): Show |
1 | a0001c0001t0002g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(42): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(5): Show |
4 | a0001c0001t0003g0290 a0001c0001t0003g0292 a0001c0001t0003g0296 others(1): Show |
4 | HG01361.hp1 NA18984.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(7): Show |
2 | a0001c0002t0002g0055 a0001c0002t0017g0051 |
2 | HG03831.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(9): Show |
2 | a0001c0002t0004g0053 a0001c0002t0054g0016 |
2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(35): Show |
1 | a0001c0001t0002g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(37): Show |
1 | a0001c0001t0002g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(7): Show |
8 | a0001c0001t0002g0196 a0001c0001t0003g0291 a0001c0001t0003g0293 others(5): Show |
8 | HG01109.hp1 HG02027.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(9): Show |
4 | a0001c0001t0004g0265 a0001c0002t0002g0027 a0001c0002t0002g0082 others(1): Show |
4 | NA18981.hp2 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(37): Show |
2 | a0001c0001t0002g0192 a0001c0001t0002g0198 |
2 | HG00639.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(46): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(9): Show |
2 | a0001c0001t0003g0303 a0001c0001t0037g0212 |
2 | HG03017.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(11): Show |
13 | a0001c0001t0001g0275 a0001c0001t0003g0268 a0001c0001t0009g0260 others(10): Show |
13 | HG00438.hp1 HG01175.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(13): Show |
1 | a0001c0002t0004g0020 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(11): Show |
4 | a0001c0001t0003g0289 a0001c0001t0003g0301 a0001c0001t0014g0298 others(1): Show |
4 | HG03209.hp1 NA18979.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(13): Show |
9 | a0001c0001t0005g0005 a0001c0001t0009g0262 a0001c0001t0023g0255 others(6): Show |
9 | HG00544.hp2 HG01258.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(15): Show |
9 | a0001c0001t0005g0005 a0001c0001t0009g0257 a0001c0001t0009g0264 others(6): Show |
9 | HG00597.hp2 HG01256.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(17): Show |
1 | a0001c0002t0004g0038 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(17): Show |
7 | a0001c0001t0009g0004 a0001c0001t0009g0278 a0001c0002t0002g0021 others(4): Show |
8 | HG00673.hp2 HG01993.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(19): Show |
1 | a0001c0001t0007g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(19): Show |
3 | a0001c0001t0003g0277 a0001c0002t0002g0026 a0001c0002t0004g0040 |
3 | HG04115.hp1 NA18612.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.743+4869_743+4870i others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(21): Show |
4 | a0001c0001t0005g0281 a0001c0002t0004g0039 a0001c0002t0017g0034 others(1): Show |
4 | HG01255.hp2 NA18942.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+4869_743+4870i others(30): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(23): Show |
1 | a0001c0002t0035g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.743+4869_743+4870i others(32): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(25): Show |
1 | a0001c0002t0047g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(34): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATATA others(35): Show |
1 | a0001c0001t0002g0208 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(44): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TATATTCA others(31): Show |
1 | a0001c0001t0002g0209 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.743+4869_743+4870i others(40): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119169 | ||||||
chr11:44119169 | T | TGTATATA others(11): Show |
1 | a0001c0001t0002g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.743+4868_743+4869i others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119169 | |||||||
chr11:44119171 | C | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0086 others(46): Show |
49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4870C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119171 | |||||||
chr11:44119173 | C | T | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4872C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119173 | |||||||
chr11:44119174 | A | G | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.743+4873A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119174 | |||||||
chr11:44119175 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0086 others(46): Show |
49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4874T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119175 | |||||||
chr11:44119175 | TAC | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
46 | HG00423.hp2 HG01109.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.743+4892_743+4893d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119175 | ||||||
chr11:44119177 | C | CAT | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.743+4877_743+4878i others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44119177 | ||||||
chr11:44119177 | C | G | 3 | a0001c0001t0006g0164 a0001c0008t0001g0162 a0001c0008t0001g0163 |
3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4876C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119177 | |||||||
chr11:44119177 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0086 others(46): Show |
49 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+4876C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119177 | |||||||
chr11:44119183 | C | T | 3 | a0001c0001t0006g0164 a0001c0008t0001g0162 a0001c0008t0001g0163 |
3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4882C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119183 | |||||||
chr11:44119191 | C | G | 55 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0003g0190 others(52): Show |
57 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.743+4890C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119191 | |||||||
chr11:44119192 | A | T | 3 | a0001c0001t0006g0164 a0001c0008t0001g0162 a0001c0008t0001g0163 |
3 | HG00438.hp2 HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.743+4891A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119192 | |||||||
chr11:44119235 | C | T | 1 | a0001c0001t0038g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.743+4934C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119235 | |||||||
chr11:44119337 | G | A | 10 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(7): Show |
11 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.743+5036G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119337 | |||||||
chr11:44119345 | A | C | 1 | a0001c0001t0052g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.743+5044A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119345 | |||||||
chr11:44119504 | T | G | 2 | a0001c0001t0023g0254 a0001c0001t0023g0255 |
2 | NA18953.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.743+5203T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119504 | |||||||
chr11:44119559 | G | A | 1 | a0001c0001t0005g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.744-5230G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119559 | |||||||
chr11:44119627 | T | C | 1 | a0001c0001t0014g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744-5162T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119627 | |||||||
chr11:44119683 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.744-5106C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119683 | |||||||
chr11:44119690 | T | C | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-5099T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119690 | |||||||
chr11:44119749 | C | A | 2 | a0001c0014t0061g0238 a0002c0005t0060g0240 |
2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-5040C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119749 | |||||||
chr11:44119827 | G | A | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.744-4962G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119827 | |||||||
chr11:44119854 | C | T | 11 | a0001c0001t0002g0251 a0001c0001t0008g0003 a0001c0001t0008g0243 others(8): Show |
12 | HG01099.hp1 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-4935C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44119854 | |||||||
chr11:44120300 | G | A | 29 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(26): Show |
29 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.744-4489G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120300 | |||||||
chr11:44120509 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.744-4280G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120509 | |||||||
chr11:44120559 | C | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0296 |
2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.744-4230C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120559 | |||||||
chr11:44120776 | C | T | 2 | a0001c0001t0005g0005 a0001c0001t0005g0281 |
3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.744-4013C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120776 | |||||||
chr11:44120912 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.744-3877C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44120912 | |||||||
chr11:44121045 | G | C | 10 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.744-3744G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121045 | |||||||
chr11:44121100 | T | C | 96 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(93): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.744-3689T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121100 | |||||||
chr11:44121146 | T | C | 1 | a0001c0001t0049g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.744-3643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121146 | |||||||
chr11:44121167 | A | C | 43 | a0001c0001t0005g0062 a0001c0001t0014g0298 a0001c0002t0002g0021 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.744-3622A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121167 | |||||||
chr11:44121187 | T | C | 7 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(4): Show |
7 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.744-3602T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121187 | |||||||
chr11:44121227 | G | A | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.744-3562G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121227 | |||||||
chr11:44121384 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.744-3405T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121384 | |||||||
chr11:44121480 | C | T | 6 | a0001c0001t0011g0309 a0001c0001t0011g0310 a0001c0001t0015g0131 others(3): Show |
6 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-3309C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121480 | |||||||
chr11:44121497 | G | A | 1 | a0001c0001t0009g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.744-3292G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121497 | |||||||
chr11:44121548 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.744-3241T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121548 | |||||||
chr11:44121951 | C | T | 8 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-2838C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44121951 | |||||||
chr11:44122056 | G | C | 1 | a0003c0006t0007g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744-2733G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122056 | |||||||
chr11:44122349 | GT | G | 3 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.744-2437delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44122349 | ||||||
chr11:44122425 | G | C | 109 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(106): Show |
110 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.744-2364G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122425 | |||||||
chr11:44122509 | A | G | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.744-2280A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122509 | |||||||
chr11:44122566 | A | G | 2 | a0001c0001t0003g0297 a0001c0001t0003g0302 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.744-2223A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122566 | |||||||
chr11:44122670 | C | T | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.744-2119C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122670 | |||||||
chr11:44122695 | T | G | 1 | a0001c0001t0008g0243 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.744-2094T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122695 | |||||||
chr11:44122927 | G | A | 3 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 |
3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.744-1862G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44122927 | |||||||
chr11:44123093 | G | A | 209 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.744-1696G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123093 | |||||||
chr11:44123148 | G | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-1641G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123148 | |||||||
chr11:44123228 | C | T | 8 | a0001c0002t0004g0030 a0001c0002t0004g0048 a0001c0002t0004g0049 others(5): Show |
8 | HG00621.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.744-1561C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123228 | |||||||
chr11:44123343 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.744-1446C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123343 | |||||||
chr11:44123484 | C | T | 1 | a0001c0001t0010g0002 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.744-1305C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123484 | |||||||
chr11:44123500 | C | A | 1 | a0001c0002t0004g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.744-1289C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44123500 | |||||||
chr11:44123773 | TCTCTGTC others(150): Show |
T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744-852_744-696del | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44123773 | ||||||
chr11:44124444 | T | TAC | 41 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(38): Show |
41 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.744-307_744-306dup others(2): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | T | TACAC | 15 | a0001c0001t0001g0012 a0001c0001t0002g0192 a0001c0001t0002g0208 others(12): Show |
15 | HG01261.hp2 HG01346.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.744-309_744-306dup others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | T | TACACAC | 35 | a0001c0001t0005g0062 a0001c0001t0005g0064 a0001c0001t0005g0065 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.744-311_744-306dup others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | T | TACACACA others(1): Show |
5 | a0001c0001t0002g0210 a0001c0001t0021g0060 a0001c0001t0021g0061 others(2): Show |
5 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.744-313_744-306dup others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | T | TACACACA others(3): Show |
11 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(8): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-315_744-306dup others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | T | TACACACA others(5): Show |
1 | a0001c0001t0014g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744-317_744-306dup others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | TAC | T | 165 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0086 others(162): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.744-307_744-306del others(2): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | TACAC | T | 9 | a0001c0001t0001g0095 a0001c0001t0006g0139 a0001c0001t0006g0157 others(6): Show |
9 | HG00621.hp1 HG02486.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.744-309_744-306del others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124444 | TACACAC | T | 12 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(9): Show |
13 | HG00639.hp2 HG02257.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.744-311_744-306del others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124444 | ||||||
chr11:44124459 | A | G | 3 | a0001c0001t0052g0252 a0001c0001t0053g0256 a0001c0014t0061g0238 |
3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.744-330A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124459 | |||||||
chr11:44124620 | TATA | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.744-165_744-163del others(3): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 44124620 | ||||||
chr11:44124706 | C | CG | 12 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(9): Show |
12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-83_744-82insG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124706 | |||||||
chr11:44124707 | A | G | 241 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.744-82A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124707 | |||||||
chr11:44124707 | A | T | 12 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(9): Show |
12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.744-82A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124707 | |||||||
chr11:44124744 | C | T | 2 | a0001c0004t0016g0172 a0001c0004t0016g0173 |
2 | HG03017.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.744-45C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 4/13 | chr11 | 44124744 | |||||||
chr11:44125007 | C | T | 8 | a0001c0003t0003g0258 a0001c0003t0003g0259 a0001c0003t0003g0269 others(5): Show |
8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+23C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125007 | |||||||
chr11:44125020 | G | T | 8 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+36G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125020 | |||||||
chr11:44125081 | A | G | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.939+97A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125081 | |||||||
chr11:44125300 | C | G | 42 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.939+316C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125300 | |||||||
chr11:44125421 | T | C | 3 | a0001c0001t0002g0179 a0001c0001t0002g0182 a0001c0001t0002g0185 |
3 | HG00741.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.939+437T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125421 | |||||||
chr11:44125451 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.939+467T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125451 | |||||||
chr11:44125513 | A | G | 46 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(43): Show |
46 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.939+529A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125513 | |||||||
chr11:44125680 | A | AT | 99 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(96): Show |
100 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.939+709dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 44125680 | ||||||
chr11:44125879 | A | G | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.939+895A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44125879 | |||||||
chr11:44126112 | T | C | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.940-704T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126112 | |||||||
chr11:44126367 | C | T | 2 | a0001c0001t0008g0246 a0001c0001t0008g0247 |
2 | NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.940-449C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126367 | |||||||
chr11:44126487 | A | C | 1 | a0001c0002t0004g0015 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.940-329A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126487 | |||||||
chr11:44126628 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.940-188A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126628 | |||||||
chr11:44126737 | A | C | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.940-79A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 5/13 | chr11 | 44126737 | |||||||
chr11:44127015 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1079+60T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127015 | |||||||
chr11:44127323 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1079+368G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127323 | |||||||
chr11:44127368 | G | A | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1079+413G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127368 | |||||||
chr11:44127779 | A | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1079+824A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127779 | |||||||
chr11:44127790 | A | AGAG | 60 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(57): Show |
60 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1079+835_1079+836i others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127790 | |||||||
chr11:44127791 | C | T | 60 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(57): Show |
60 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1079+836C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127791 | |||||||
chr11:44127796 | C | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1079+841C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44127796 | |||||||
chr11:44128050 | T | A | 1 | a0001c0001t0003g0274 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1079+1095T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128050 | |||||||
chr11:44128295 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1079+1340C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128295 | |||||||
chr11:44128547 | C | G | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080-1498C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128547 | |||||||
chr11:44128954 | G | A | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1080-1091G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128954 | |||||||
chr11:44128980 | A | T | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1080-1065A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128980 | |||||||
chr11:44128981 | G | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080-1064G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44128981 | |||||||
chr11:44129022 | C | T | 312 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1080-1023C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129022 | |||||||
chr11:44129185 | C | T | 150 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0003g0190 others(147): Show |
154 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1080-860C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129185 | |||||||
chr11:44129369 | T | C | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1080-676T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129369 | |||||||
chr11:44129431 | G | A | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1080-614G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129431 | |||||||
chr11:44129465 | C | T | 3 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-580C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129465 | |||||||
chr11:44129466 | T | C | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1080-579T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129466 | |||||||
chr11:44129531 | T | G | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1080-514T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129531 | |||||||
chr11:44129674 | C | T | 310 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(307): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.1080-371C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129674 | |||||||
chr11:44129907 | T | C | 312 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1080-138T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129907 | |||||||
chr11:44129912 | CT | C | 6 | a0001c0002t0004g0001 a0001c0002t0004g0029 a0001c0002t0004g0032 others(3): Show |
7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-131delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 44129912 | ||||||
chr11:44129930 | G | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(79): Show |
82 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1080-115G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44129930 | |||||||
chr11:44130027 | T | A | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(97): Show |
101 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1080-18T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 6/13 | chr11 | 44130027 | |||||||
chr11:44130309 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0126 |
2 | HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1173+171G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130309 | |||||||
chr11:44130365 | G | A | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+227G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130365 | |||||||
chr11:44130379 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1173+241C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130379 | |||||||
chr11:44130512 | T | G | 26 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(23): Show |
26 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1173+374T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130512 | |||||||
chr11:44130555 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1173+417T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130555 | |||||||
chr11:44130559 | G | A | 3 | a0001c0001t0052g0252 a0001c0001t0053g0256 a0001c0014t0061g0238 |
3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44130559 | |||||||
chr11:44131106 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1173+968G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131106 | |||||||
chr11:44131146 | CTT | C | 3 | a0001c0001t0009g0262 a0001c0001t0009g0264 a0001c0001t0041g0261 |
3 | HG00544.hp2 NA19005.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1173+1009_1173+101 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131146 | |||||||
chr11:44131456 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(86): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+1318C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131456 | |||||||
chr11:44131499 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+1361T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131499 | |||||||
chr11:44131908 | T | G | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1173+1770T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131908 | |||||||
chr11:44131938 | A | T | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+1800A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131938 | |||||||
chr11:44131983 | G | A | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1173+1845G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44131983 | |||||||
chr11:44132179 | A | G | 49 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(46): Show |
49 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1173+2041A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132179 | |||||||
chr11:44132508 | C | T | 3 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1173+2370C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132508 | |||||||
chr11:44132682 | C | T | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+2544C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132682 | |||||||
chr11:44132879 | C | T | 4 | a0001c0001t0006g0136 a0001c0001t0006g0138 a0001c0001t0006g0142 others(1): Show |
4 | NA18942.hp1 NA18966.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+2741C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132879 | |||||||
chr11:44132908 | C | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+2770C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44132908 | |||||||
chr11:44133276 | A | C | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1173+3138A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133276 | |||||||
chr11:44133733 | G | A | 97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(94): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1173+3595G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133733 | |||||||
chr11:44133744 | A | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+3606A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133744 | |||||||
chr11:44133845 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1173+3707A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133845 | |||||||
chr11:44133885 | C | T | 43 | a0001c0001t0004g0325 a0001c0002t0002g0021 a0001c0002t0002g0023 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1173+3747C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133885 | |||||||
chr11:44133886 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1173+3748G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133886 | |||||||
chr11:44133904 | A | G | 1 | a0001c0001t0007g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1173+3766A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44133904 | |||||||
chr11:44134049 | C | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+3911C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134049 | |||||||
chr11:44134053 | G | T | 1 | a0001c0001t0008g0249 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1173+3915G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134053 | |||||||
chr11:44134059 | G | T | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1173+3921G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134059 | |||||||
chr11:44134075 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(86): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+3937G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134075 | |||||||
chr11:44134101 | C | T | 138 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0002g0089 others(135): Show |
141 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1173+3963C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134101 | |||||||
chr11:44134275 | G | T | 9 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+4137G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134275 | |||||||
chr11:44134317 | AT | A | 9 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+4180delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134317 | |||||||
chr11:44134395 | C | T | 51 | a0001c0001t0001g0176 a0001c0001t0001g0275 a0001c0001t0003g0190 others(48): Show |
53 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1173+4257C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134395 | |||||||
chr11:44134479 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+4341T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134479 | |||||||
chr11:44134987 | G | A | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+4849G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44134987 | |||||||
chr11:44135149 | G | A | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+5011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135149 | |||||||
chr11:44135206 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1173+5068G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135206 | |||||||
chr11:44135390 | C | CT | 7 | a0001c0001t0003g0193 a0001c0001t0003g0224 a0001c0001t0003g0225 others(4): Show |
7 | HG01243.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+5271dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | ||||||
chr11:44135390 | C | CTT | 10 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(7): Show |
10 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1173+5270_1173+527 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | ||||||
chr11:44135390 | CT | C | 266 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1173+5271delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44135390 | ||||||
chr11:44135392 | T | TC | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+5254_1173+525 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135392 | |||||||
chr11:44135474 | C | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(86): Show |
89 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1173+5336C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135474 | |||||||
chr11:44135478 | G | C | 1 | a0001c0001t0007g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1173+5340G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135478 | |||||||
chr11:44135501 | C | T | 1 | a0002c0005t0019g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1173+5363C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135501 | |||||||
chr11:44135579 | A | G | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+5441A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135579 | |||||||
chr11:44135805 | G | A | 312 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.1173+5667G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135805 | |||||||
chr11:44135955 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1173+5817T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44135955 | |||||||
chr11:44136050 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1173+5912A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136050 | |||||||
chr11:44136240 | C | A | 1 | a0001c0001t0007g0319 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1173+6102C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136240 | |||||||
chr11:44136519 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1173+6381C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136519 | |||||||
chr11:44136603 | C | G | 35 | a0001c0001t0003g0213 a0001c0001t0005g0019 a0001c0001t0005g0062 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1173+6465C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136603 | |||||||
chr11:44136653 | A | G | 1 | a0001c0002t0017g0046 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1173+6515A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136653 | |||||||
chr11:44136888 | A | G | 83 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(80): Show |
83 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1173+6750A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44136888 | |||||||
chr11:44137000 | A | G | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+6862A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137000 | |||||||
chr11:44137017 | A | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+6879A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137017 | |||||||
chr11:44137188 | T | A | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+7050T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137188 | |||||||
chr11:44137453 | G | A | 4 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(1): Show |
4 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+7315G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137453 | |||||||
chr11:44137581 | G | C | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+7443G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137581 | |||||||
chr11:44137644 | C | T | 1 | a0001c0001t0009g0288 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1173+7506C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137644 | |||||||
chr11:44137776 | G | T | 3 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1173+7638G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44137776 | |||||||
chr11:44138284 | A | G | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1173+8146A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138284 | |||||||
chr11:44138558 | A | T | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1173+8420A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138558 | |||||||
chr11:44138770 | G | A | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+8632G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44138770 | |||||||
chr11:44139120 | C | CT | 95 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0001g0176 others(92): Show |
98 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1173+8995dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139120 | ||||||
chr11:44139120 | C | CTT | 44 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(41): Show |
44 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1173+8994_1173+899 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139120 | ||||||
chr11:44139135 | C | T | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1173+8997C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139135 | |||||||
chr11:44139198 | CT | C | 6 | a0001c0002t0002g0027 a0001c0002t0004g0015 a0002c0005t0019g0236 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+9073delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44139198 | ||||||
chr11:44139352 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1173+9214C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139352 | |||||||
chr11:44139402 | G | A | 6 | a0001c0001t0002g0205 a0001c0001t0008g0203 a0001c0001t0008g0234 others(3): Show |
6 | NA18986.hp2 NA18999.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+9264G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139402 | |||||||
chr11:44139734 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0040g0025 |
2 | NA18942.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1173+9596C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44139734 | |||||||
chr11:44140315 | C | T | 4 | a0001c0002t0004g0022 a0001c0002t0004g0043 a0001c0002t0004g0044 others(1): Show |
4 | HG02027.hp1 NA18990.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10177C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140315 | |||||||
chr11:44140751 | T | G | 53 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(50): Show |
53 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1173+10613T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140751 | |||||||
chr11:44140797 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1173+10659A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140797 | |||||||
chr11:44140833 | A | C | 4 | a0001c0001t0012g0090 a0001c0001t0012g0107 a0001c0001t0012g0108 others(1): Show |
4 | HG01978.hp2 HG01993.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+10695A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44140833 | |||||||
chr11:44140936 | TTATAGTA others(15): Show |
T | 1 | a0001c0001t0023g0255 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1173+10804_1173+10 others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44140936 | ||||||
chr11:44141023 | C | T | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+10885C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141023 | |||||||
chr11:44141079 | T | C | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+10941T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141079 | |||||||
chr11:44141189 | C | T | 7 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1173+11051C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141189 | |||||||
chr11:44141289 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1173+11151T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141289 | |||||||
chr11:44141307 | A | G | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+11169A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141307 | |||||||
chr11:44141323 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+11185A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141323 | |||||||
chr11:44141390 | GA | G | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+11253delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141390 | |||||||
chr11:44141454 | A | C | 12 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(9): Show |
13 | HG02896.hp1 HG02970.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+11316A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141454 | |||||||
chr11:44141535 | A | G | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+11397A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141535 | |||||||
chr11:44141668 | C | T | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1173+11530C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141668 | |||||||
chr11:44141671 | A | G | 1 | a0001c0001t0006g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1173+11533A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141671 | |||||||
chr11:44141704 | C | T | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+11566C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141704 | |||||||
chr11:44141721 | G | A | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+11583G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141721 | |||||||
chr11:44141839 | C | A | 1 | a0001c0001t0034g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1173+11701C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141839 | |||||||
chr11:44141896 | A | G | 4 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0022g0327 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+11758A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141896 | |||||||
chr11:44141988 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1173+11850G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44141988 | |||||||
chr11:44142156 | A | C | 1 | a0001c0001t0003g0289 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1173+12018A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142156 | |||||||
chr11:44142267 | T | C | 5 | a0001c0001t0010g0059 a0001c0001t0021g0060 a0001c0001t0021g0061 others(2): Show |
5 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+12129T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142267 | |||||||
chr11:44142278 | C | T | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+12140C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142278 | |||||||
chr11:44142287 | T | C | 180 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(177): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1173+12149T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142287 | |||||||
chr11:44142347 | T | G | 1 | a0001c0001t0009g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1173+12209T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142347 | |||||||
chr11:44142352 | A | G | 33 | a0001c0001t0003g0190 a0001c0001t0003g0268 a0001c0001t0003g0274 others(30): Show |
35 | HG00323.hp2 HG00544.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1173+12214A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142352 | |||||||
chr11:44142482 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1173+12344T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142482 | |||||||
chr11:44142873 | C | T | 1 | a0001c0001t0008g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1173+12735C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44142873 | |||||||
chr11:44143013 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1173+12875G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143013 | |||||||
chr11:44143050 | C | T | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+12912C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143050 | |||||||
chr11:44143078 | A | T | 1 | a0001c0002t0035g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1173+12940A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143078 | |||||||
chr11:44143088 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+12950A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143088 | |||||||
chr11:44143350 | T | C | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1173+13212T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143350 | |||||||
chr11:44143363 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+13225G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143363 | |||||||
chr11:44143589 | A | G | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1173+13451A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143589 | |||||||
chr11:44143815 | G | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+13677G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143815 | |||||||
chr11:44143945 | A | T | 55 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(52): Show |
55 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1173+13807A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44143945 | |||||||
chr11:44144056 | G | A | 1 | a0001c0002t0004g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1173+13918G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144056 | |||||||
chr11:44144142 | C | T | 1 | a0001c0001t0009g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173+14004C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144142 | |||||||
chr11:44144144 | C | T | 1 | a0001c0001t0009g0282 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1173+14006C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144144 | |||||||
chr11:44144644 | C | T | 2 | a0001c0001t0006g0139 a0001c0001t0006g0157 |
2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1173+14506C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144644 | |||||||
chr11:44144892 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1173+14754A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144892 | |||||||
chr11:44144982 | A | G | 1 | a0001c0001t0058g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1173+14844A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44144982 | |||||||
chr11:44145278 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1173+15140C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145278 | |||||||
chr11:44145285 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+15147T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145285 | |||||||
chr11:44145352 | A | C | 1 | a0001c0001t0051g0148 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1173+15214A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145352 | |||||||
chr11:44145447 | A | G | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1173+15309A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145447 | |||||||
chr11:44145717 | G | A | 4 | a0001c0001t0004g0265 a0001c0001t0009g0004 a0001c0001t0009g0257 others(1): Show |
5 | HG02523.hp2 NA18973.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+15579G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145717 | |||||||
chr11:44145744 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1173+15606A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145744 | |||||||
chr11:44145802 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1173+15664T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145802 | |||||||
chr11:44145904 | T | C | 15 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(12): Show |
15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+15766T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145904 | |||||||
chr11:44145993 | A | C | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+15855A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44145993 | |||||||
chr11:44146446 | C | T | 179 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(176): Show |
183 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1173+16308C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146446 | |||||||
chr11:44146524 | G | C | 1 | a0001c0001t0007g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1173+16386G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146524 | |||||||
chr11:44146553 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1173+16415G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146553 | |||||||
chr11:44146649 | C | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1173+16511C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146649 | |||||||
chr11:44146857 | T | A | 2 | a0001c0001t0005g0005 a0001c0001t0005g0281 |
3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1173+16719T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44146857 | |||||||
chr11:44147108 | T | G | 3 | a0001c0001t0015g0219 a0001c0001t0015g0222 a0001c0001t0015g0223 |
3 | HG02257.hp1 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1173+16970T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147108 | |||||||
chr11:44147259 | A | G | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+17121A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147259 | |||||||
chr11:44147449 | C | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1173+17311C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147449 | |||||||
chr11:44147498 | A | G | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1173+17360A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147498 | |||||||
chr11:44147562 | TTTG | T | 51 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(48): Show |
53 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1173+17436_1173+17 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147562 | ||||||
chr11:44147646 | C | T | 13 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+17508C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147646 | |||||||
chr11:44147706 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0151 a0001c0001t0001g0165 others(1): Show |
4 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1173+17568G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147706 | |||||||
chr11:44147726 | A | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
91 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1173+17588A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147726 | |||||||
chr11:44147727 | AT | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1173+17602delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147727 | ||||||
chr11:44147775 | C | CTTTT | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(162): Show |
167 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1173+17649_1173+17 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | ||||||
chr11:44147775 | C | CTTTTT | 108 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0176 others(105): Show |
111 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1173+17648_1173+17 others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | ||||||
chr11:44147775 | C | CTTTTTT | 16 | a0001c0001t0002g0110 a0001c0001t0002g0205 a0001c0001t0002g0211 others(13): Show |
16 | HG01243.hp2 HG02135.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1173+17647_1173+17 others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | ||||||
chr11:44147775 | C | CTTTTTTT | 15 | a0001c0001t0003g0231 a0001c0001t0018g0312 a0001c0001t0018g0313 others(12): Show |
15 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+17646_1173+17 others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44147775 | ||||||
chr11:44147883 | A | G | 3 | a0001c0001t0005g0069 a0001c0001t0005g0070 a0001c0001t0038g0071 |
3 | HG02280.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1173+17745A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44147883 | |||||||
chr11:44148112 | G | A | 12 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(9): Show |
13 | HG02896.hp1 HG02970.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.1173+17974G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148112 | |||||||
chr11:44148191 | A | G | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1173+18053A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148191 | |||||||
chr11:44148192 | G | C | 1 | a0001c0014t0061g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1173+18054G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148192 | |||||||
chr11:44148239 | T | C | 296 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(293): Show |
301 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.1173+18101T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148239 | |||||||
chr11:44148248 | C | A | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+18110C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148248 | |||||||
chr11:44148286 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1173+18148A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148286 | |||||||
chr11:44148372 | G | C | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+18234G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148372 | |||||||
chr11:44148465 | G | A | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173+18327G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148465 | |||||||
chr11:44148647 | G | A | 9 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+18509G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148647 | |||||||
chr11:44148709 | G | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+18571G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148709 | |||||||
chr11:44148803 | A | G | 2 | a0001c0001t0013g0007 a0001c0001t0013g0008 |
2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1173+18665A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44148803 | |||||||
chr11:44149116 | C | G | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1173+18978C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149116 | |||||||
chr11:44149254 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1173+19116C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149254 | |||||||
chr11:44149395 | A | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1173+19257A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149395 | |||||||
chr11:44149459 | G | A | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+19321G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149459 | |||||||
chr11:44149505 | T | C | 1 | a0001c0001t0006g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1173+19367T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149505 | |||||||
chr11:44149599 | T | C | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1173+19461T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149599 | |||||||
chr11:44149610 | A | G | 2 | a0001c0001t0009g0280 a0001c0001t0042g0279 |
2 | NA19000.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1173+19472A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149610 | |||||||
chr11:44149754 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1173+19616T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149754 | |||||||
chr11:44149774 | C | T | 16 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(13): Show |
17 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1173+19636C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149774 | |||||||
chr11:44149799 | A | G | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+19661A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149799 | |||||||
chr11:44149906 | T | C | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(100): Show |
104 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1173+19768T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44149906 | |||||||
chr11:44150149 | G | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+20011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150149 | |||||||
chr11:44150274 | T | A | 43 | a0001c0001t0004g0325 a0001c0002t0002g0021 a0001c0002t0002g0023 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1173+20136T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150274 | |||||||
chr11:44150281 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1173+20143T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150281 | |||||||
chr11:44150302 | CT | C | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1173+20173delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44150302 | ||||||
chr11:44150396 | T | C | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+20258T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150396 | |||||||
chr11:44150455 | G | A | 1 | a0001c0001t0031g0217 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1173+20317G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150455 | |||||||
chr11:44150613 | A | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1173+20475A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150613 | |||||||
chr11:44150662 | C | T | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+20524C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150662 | |||||||
chr11:44150861 | G | A | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1173+20723G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150861 | |||||||
chr11:44150996 | G | A | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1174-20615G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44150996 | |||||||
chr11:44151065 | T | G | 2 | a0001c0001t0007g0322 a0001c0001t0007g0323 |
2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1174-20546T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151065 | |||||||
chr11:44151266 | A | T | 1 | a0001c0001t0005g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1174-20345A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151266 | |||||||
chr11:44151291 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-20320C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151291 | |||||||
chr11:44151453 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-20158G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151453 | |||||||
chr11:44151476 | T | C | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-20135T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151476 | |||||||
chr11:44151506 | C | T | 251 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1174-20105C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151506 | |||||||
chr11:44151767 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1174-19844G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44151767 | |||||||
chr11:44152128 | T | A | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1174-19483T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152128 | |||||||
chr11:44152167 | A | G | 1 | a0001c0001t0003g0290 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1174-19444A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152167 | |||||||
chr11:44152343 | G | GGTT | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-19246_1174-19 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44152343 | ||||||
chr11:44152511 | C | T | 1 | a0001c0001t0006g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1174-19100C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152511 | |||||||
chr11:44152512 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-19099G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152512 | |||||||
chr11:44152527 | T | C | 180 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(177): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1174-19084T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152527 | |||||||
chr11:44152531 | A | G | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1174-19080A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152531 | |||||||
chr11:44152597 | C | T | 180 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(177): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1174-19014C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152597 | |||||||
chr11:44152602 | C | T | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-19009C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152602 | |||||||
chr11:44152627 | G | A | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(114): Show |
118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1174-18984G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152627 | |||||||
chr11:44152834 | A | G | 60 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(57): Show |
60 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174-18777A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152834 | |||||||
chr11:44152862 | G | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-18749G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152862 | |||||||
chr11:44152910 | A | G | 2 | a0001c0002t0004g0031 a0001c0002t0004g0042 |
2 | HG00438.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1174-18701A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152910 | |||||||
chr11:44152954 | T | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-18657T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44152954 | |||||||
chr11:44153052 | A | G | 180 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(177): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1174-18559A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153052 | |||||||
chr11:44153084 | G | A | 45 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(42): Show |
45 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-18527G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153084 | |||||||
chr11:44153115 | G | A | 15 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(12): Show |
15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-18496G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153115 | |||||||
chr11:44153131 | T | C | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-18480T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153131 | |||||||
chr11:44153493 | A | G | 1 | a0001c0001t0012g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1174-18118A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153493 | |||||||
chr11:44153873 | T | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-17738T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153873 | |||||||
chr11:44153925 | T | G | 60 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(57): Show |
60 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174-17686T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153925 | |||||||
chr11:44153938 | T | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-17673T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153938 | |||||||
chr11:44153965 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-17646A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44153965 | |||||||
chr11:44154073 | G | T | 1 | a0001c0001t0022g0327 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1174-17538G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154073 | |||||||
chr11:44154145 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1174-17466G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154145 | |||||||
chr11:44154207 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1174-17404C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154207 | |||||||
chr11:44154392 | A | G | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1174-17219A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154392 | |||||||
chr11:44154495 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-17116C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154495 | |||||||
chr11:44154593 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-17018T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154593 | |||||||
chr11:44154787 | T | A | 1 | a0001c0001t0005g0062 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1174-16824T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154787 | |||||||
chr11:44154851 | T | G | 60 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(57): Show |
60 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1174-16760T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44154851 | |||||||
chr11:44155263 | T | G | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1174-16348T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155263 | |||||||
chr11:44155504 | A | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1174-16107A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155504 | |||||||
chr11:44155785 | G | A | 135 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(132): Show |
139 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1174-15826G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155785 | |||||||
chr11:44155821 | A | G | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1174-15790A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155821 | |||||||
chr11:44155883 | G | A | 2 | a0001c0002t0002g0035 a0001c0002t0002g0036 |
2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1174-15728G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155883 | |||||||
chr11:44155886 | T | C | 1 | a0001c0002t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1174-15725T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44155886 | |||||||
chr11:44156197 | G | C | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-15414G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156197 | |||||||
chr11:44156505 | T | C | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-15106T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156505 | |||||||
chr11:44156644 | A | G | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1174-14967A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156644 | |||||||
chr11:44156777 | G | A | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-14834G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156777 | |||||||
chr11:44156868 | A | T | 1 | a0001c0001t0003g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1174-14743A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156868 | |||||||
chr11:44156875 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1174-14736C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156875 | |||||||
chr11:44156940 | G | C | 2 | a0001c0002t0004g0043 a0001c0002t0004g0044 |
2 | NA19066.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1174-14671G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156940 | |||||||
chr11:44156963 | C | G | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1174-14648C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44156963 | |||||||
chr11:44157074 | C | T | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-14537C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157074 | |||||||
chr11:44157086 | G | A | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-14525G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157086 | |||||||
chr11:44157316 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1174-14295C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157316 | |||||||
chr11:44157417 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1174-14194C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157417 | |||||||
chr11:44157556 | C | T | 1 | a0001c0001t0013g0006 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1174-14055C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157556 | |||||||
chr11:44157602 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1174-14009C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44157602 | |||||||
chr11:44158172 | G | A | 1 | a0001c0002t0004g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1174-13439G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158172 | |||||||
chr11:44158185 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-13426T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158185 | |||||||
chr11:44158212 | A | T | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-13399A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158212 | |||||||
chr11:44158431 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-13180G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158431 | |||||||
chr11:44158547 | AATTT | A | 12 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(9): Show |
12 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1174-13062_1174-13 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44158547 | ||||||
chr11:44158726 | A | G | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1174-12885A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158726 | |||||||
chr11:44158775 | G | A | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1174-12836G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158775 | |||||||
chr11:44158822 | C | G | 1 | a0001c0001t0018g0313 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1174-12789C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158822 | |||||||
chr11:44158877 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1174-12734T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44158877 | |||||||
chr11:44159004 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1174-12607T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159004 | |||||||
chr11:44159118 | G | A | 44 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(41): Show |
44 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1174-12493G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159118 | |||||||
chr11:44159121 | CT | C | 61 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0002g0089 others(58): Show |
62 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1174-12477delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44159121 | ||||||
chr11:44159151 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-12460T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159151 | |||||||
chr11:44159180 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | HG00621.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1174-12431G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159180 | |||||||
chr11:44159188 | T | C | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-12423T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159188 | |||||||
chr11:44159346 | CT | C | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-12256delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44159346 | ||||||
chr11:44159478 | A | G | 148 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(145): Show |
152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1174-12133A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159478 | |||||||
chr11:44159719 | G | A | 1 | a0001c0001t0006g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1174-11892G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159719 | |||||||
chr11:44159771 | G | C | 43 | a0001c0001t0004g0325 a0001c0002t0002g0021 a0001c0002t0002g0023 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1174-11840G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44159771 | |||||||
chr11:44160141 | G | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1174-11470G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160141 | |||||||
chr11:44160202 | G | A | 1 | a0001c0004t0029g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-11409G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160202 | |||||||
chr11:44160467 | A | G | 143 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(140): Show |
147 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1174-11144A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160467 | |||||||
chr11:44160830 | A | G | 1 | a0001c0002t0002g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1174-10781A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160830 | |||||||
chr11:44160870 | C | T | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-10741C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160870 | |||||||
chr11:44160933 | T | A | 144 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(141): Show |
148 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1174-10678T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44160933 | |||||||
chr11:44161108 | A | C | 53 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(50): Show |
53 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.1174-10503A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161108 | |||||||
chr11:44161177 | A | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0206 |
2 | HG03654.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1174-10434A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161177 | |||||||
chr11:44161433 | G | A | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-10178G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161433 | |||||||
chr11:44161620 | C | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-9991C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161620 | |||||||
chr11:44161759 | G | A | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-9852G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161759 | |||||||
chr11:44161993 | A | T | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-9618A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44161993 | |||||||
chr11:44162059 | C | T | 1 | a0001c0001t0014g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174-9552C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162059 | |||||||
chr11:44162140 | G | C | 12 | a0001c0001t0003g0289 a0001c0001t0003g0290 a0001c0001t0003g0291 others(9): Show |
12 | HG02027.hp2 HG02135.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-9471G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162140 | |||||||
chr11:44162402 | T | C | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1174-9209T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162402 | |||||||
chr11:44162575 | C | CA | 13 | a0001c0001t0001g0134 a0001c0001t0002g0210 a0001c0001t0003g0230 others(10): Show |
13 | HG00597.hp2 HG01167.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1174-9015dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44162575 | ||||||
chr11:44162575 | CA | C | 11 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0008g0003 others(8): Show |
12 | HG03491.hp1 HG03492.hp1 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1174-9015delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44162575 | ||||||
chr11:44162609 | T | C | 1 | a0001c0002t0002g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1174-9002T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162609 | |||||||
chr11:44162794 | A | G | 57 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(54): Show |
57 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1174-8817A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162794 | |||||||
chr11:44162896 | C | T | 1 | a0001c0001t0007g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1174-8715C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162896 | |||||||
chr11:44162897 | G | A | 1 | a0001c0004t0039g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1174-8714G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162897 | |||||||
chr11:44162979 | G | C | 57 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(54): Show |
57 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1174-8632G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44162979 | |||||||
chr11:44163224 | C | G | 1 | a0001c0001t0002g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1174-8387C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163224 | |||||||
chr11:44163312 | G | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1174-8299G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163312 | |||||||
chr11:44163528 | C | A | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1174-8083C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163528 | |||||||
chr11:44163690 | A | C | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-7921A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163690 | |||||||
chr11:44163726 | G | A | 1 | a0001c0001t0005g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1174-7885G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163726 | |||||||
chr11:44163754 | G | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-7857G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163754 | |||||||
chr11:44163977 | C | T | 1 | a0001c0004t0029g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1174-7634C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163977 | |||||||
chr11:44163999 | G | A | 1 | a0001c0001t0010g0002 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1174-7612G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44163999 | |||||||
chr11:44164238 | A | G | 50 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(47): Show |
52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1174-7373A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164238 | |||||||
chr11:44164284 | T | G | 1 | a0001c0001t0012g0161 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1174-7327T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164284 | |||||||
chr11:44164291 | T | C | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-7320T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164291 | |||||||
chr11:44164301 | C | G | 50 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(47): Show |
50 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1174-7310C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164301 | |||||||
chr11:44164366 | T | C | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1174-7245T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164366 | |||||||
chr11:44164467 | C | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-7144C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164467 | |||||||
chr11:44164781 | C | T | 2 | a0001c0001t0007g0319 a0001c0001t0007g0320 |
2 | HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1174-6830C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44164781 | |||||||
chr11:44164876 | C | CT | 10 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0001g0151 others(7): Show |
10 | HG01261.hp1 HG01361.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-6715dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44164876 | ||||||
chr11:44164876 | CT | C | 6 | a0001c0001t0001g0096 a0001c0001t0001g0159 a0001c0001t0001g0167 others(3): Show |
6 | HG00323.hp1 HG01256.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-6715delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44164876 | ||||||
chr11:44165068 | C | T | 1 | a0001c0001t0038g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1174-6543C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165068 | |||||||
chr11:44165089 | G | A | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165089 | |||||||
chr11:44165120 | C | T | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-6491C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165120 | |||||||
chr11:44165129 | C | T | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6482C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165129 | |||||||
chr11:44165183 | T | C | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6428T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165183 | |||||||
chr11:44165283 | G | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-6328G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165283 | |||||||
chr11:44165311 | T | A | 2 | a0001c0008t0001g0162 a0001c0008t0001g0163 |
2 | HG00438.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1174-6300T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165311 | |||||||
chr11:44165315 | T | G | 3 | a0001c0001t0003g0230 a0001c0001t0003g0297 a0001c0001t0003g0302 |
3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-6296T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165315 | |||||||
chr11:44165335 | A | G | 10 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(7): Show |
10 | HG01993.hp2 HG02074.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.1174-6276A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165335 | |||||||
chr11:44165352 | G | T | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-6259G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165352 | |||||||
chr11:44165361 | T | C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0120 others(2): Show |
5 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-6250T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165361 | |||||||
chr11:44165364 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-6247T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165364 | |||||||
chr11:44165596 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1174-6015C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165596 | |||||||
chr11:44165721 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1174-5890A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165721 | |||||||
chr11:44165815 | A | G | 1 | a0003c0006t0055g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-5796A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165815 | |||||||
chr11:44165852 | T | C | 97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(94): Show |
98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1174-5759T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165852 | |||||||
chr11:44165947 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0168 |
2 | NA18987.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1174-5664T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44165947 | |||||||
chr11:44166179 | C | T | 1 | a0001c0007t0005g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-5432C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166179 | |||||||
chr11:44166788 | T | G | 45 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(42): Show |
45 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1174-4823T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166788 | |||||||
chr11:44166847 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1174-4764T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166847 | |||||||
chr11:44166854 | G | A | 2 | a0001c0001t0003g0274 a0001c0001t0003g0277 |
2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1174-4757G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166854 | |||||||
chr11:44166922 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-4689C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166922 | |||||||
chr11:44166979 | C | G | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-4632C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44166979 | |||||||
chr11:44167115 | C | T | 4 | a0001c0001t0005g0065 a0001c0001t0005g0068 a0001c0001t0014g0066 others(1): Show |
4 | HG00099.hp2 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-4496C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167115 | |||||||
chr11:44167151 | T | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-4460T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167151 | |||||||
chr11:44167241 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1174-4370C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167241 | |||||||
chr11:44167402 | C | T | 3 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 |
3 | HG02145.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1174-4209C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167402 | |||||||
chr11:44167845 | G | C | 1 | a0001c0001t0008g0003 | 2 | NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1174-3766G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167845 | |||||||
chr11:44167915 | T | C | 4 | a0001c0001t0009g0260 a0001c0001t0009g0266 a0001c0001t0009g0267 others(1): Show |
4 | NA18945.hp2 NA18982.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-3696T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44167915 | |||||||
chr11:44167973 | CCCCCGA | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-3633_1174-362 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44167973 | ||||||
chr11:44168024 | A | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(90): Show |
93 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1174-3587A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168024 | |||||||
chr11:44168119 | G | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1174-3492G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168119 | |||||||
chr11:44168185 | A | G | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1174-3426A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168185 | |||||||
chr11:44168214 | GT | G | 183 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(180): Show |
187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1174-3394delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44168214 | ||||||
chr11:44168361 | A | G | 15 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(12): Show |
15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-3250A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168361 | |||||||
chr11:44168682 | G | A | 8 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(5): Show |
8 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2929G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168682 | |||||||
chr11:44168813 | A | G | 4 | a0001c0001t0013g0006 a0001c0001t0013g0007 a0001c0001t0013g0008 others(1): Show |
4 | HG01123.hp2 HG01168.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-2798A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168813 | |||||||
chr11:44168865 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1174-2746A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168865 | |||||||
chr11:44168867 | G | A | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1174-2744G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168867 | |||||||
chr11:44168908 | C | T | 3 | a0001c0001t0003g0230 a0001c0001t0003g0297 a0001c0001t0003g0302 |
3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1174-2703C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44168908 | |||||||
chr11:44169081 | G | A | 1 | a0001c0001t0007g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1174-2530G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169081 | |||||||
chr11:44169174 | C | T | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-2437C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169174 | |||||||
chr11:44169175 | G | A | 1 | a0001c0002t0048g0028 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1174-2436G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169175 | |||||||
chr11:44169345 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1174-2266T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169345 | |||||||
chr11:44169366 | C | T | 1 | a0001c0001t0006g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1174-2245C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169366 | |||||||
chr11:44169453 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0005g0214 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1174-2158C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169453 | |||||||
chr11:44169674 | G | A | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-1937G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169674 | |||||||
chr11:44169762 | T | C | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1174-1849T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169762 | |||||||
chr11:44169829 | A | AG | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1174-1782_1174-178 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169829 | |||||||
chr11:44169904 | G | A | 19 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(16): Show |
20 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1174-1707G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44169904 | |||||||
chr11:44170047 | A | C | 1 | a0001c0001t0002g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1174-1564A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170047 | |||||||
chr11:44170150 | C | T | 43 | a0001c0001t0004g0325 a0001c0002t0002g0021 a0001c0002t0002g0023 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1174-1461C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170150 | |||||||
chr11:44170166 | C | T | 1 | a0004c0012t0002g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1174-1445C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170166 | |||||||
chr11:44170167 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0168 |
2 | NA18987.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1174-1444G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170167 | |||||||
chr11:44170357 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1174-1254T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170357 | |||||||
chr11:44170363 | A | G | 1 | a0001c0001t0011g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1174-1248A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170363 | |||||||
chr11:44170665 | G | A | 8 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(5): Show |
8 | HG02145.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-946G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170665 | |||||||
chr11:44170701 | A | C | 3 | a0001c0001t0005g0064 a0001c0001t0025g0018 a0001c0001t0025g0083 |
3 | HG01346.hp1 HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1174-910A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170701 | |||||||
chr11:44170703 | C | CAT | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1174-905_1174-904d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170703 | ||||||
chr11:44170769 | G | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-842G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170769 | |||||||
chr11:44170794 | T | A | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-817T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170794 | |||||||
chr11:44170810 | TCA | T | 5 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0001c0001t0007g0322 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-755_1174-754d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACA | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(89): Show |
92 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1174-757_1174-754d others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACA | T | 18 | a0001c0001t0002g0152 a0001c0001t0002g0192 a0001c0001t0005g0064 others(15): Show |
19 | HG00735.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1174-759_1174-754d others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACAC others(1): Show |
T | 16 | a0001c0001t0002g0182 a0001c0001t0002g0187 a0001c0001t0002g0200 others(13): Show |
16 | HG00099.hp2 HG00741.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1174-761_1174-754d others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACAC others(3): Show |
T | 76 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(73): Show |
78 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1174-763_1174-754d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACAC others(5): Show |
T | 93 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(90): Show |
95 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1174-765_1174-754d others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACAC others(9): Show |
T | 5 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(2): Show |
5 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-769_1174-754d others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170810 | TCACACAC others(19): Show |
T | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-779_1174-754d others(28): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170810 | ||||||
chr11:44170837 | C | G | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174-774C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170837 | |||||||
chr11:44170837 | C | T | 4 | a0001c0001t0014g0081 a0001c0007t0005g0147 a0001c0007t0005g0221 others(1): Show |
4 | HG01261.hp1 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-774C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170837 | |||||||
chr11:44170847 | C | G | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1174-764C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44170847 | |||||||
chr11:44170848 | ACACACAC others(2): Show |
A | 3 | a0001c0001t0008g0245 a0001c0001t0013g0007 a0001c0002t0004g0057 |
3 | HG00597.hp2 HG02615.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1174-760_1174-752d others(11): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44170848 | ||||||
chr11:44171025 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1174-586C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171025 | |||||||
chr11:44171157 | G | A | 182 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(179): Show |
186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1174-454G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171157 | |||||||
chr11:44171254 | A | G | 15 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(12): Show |
15 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1174-357A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171254 | |||||||
chr11:44171303 | A | G | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1174-308A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171303 | |||||||
chr11:44171341 | C | A | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1174-270C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171341 | |||||||
chr11:44171494 | TCC | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-115_1174-114d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr11 | 44171494 | ||||||
chr11:44171593 | G | T | 1 | a0001c0001t0002g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1174-18G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 7/13 | chr11 | 44171593 | |||||||
chr11:44171868 | T | C | 6 | a0001c0001t0005g0064 a0001c0001t0010g0059 a0001c0001t0021g0060 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+126T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44171868 | |||||||
chr11:44171996 | G | C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0120 others(2): Show |
5 | HG01123.hp1 HG01167.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+254G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44171996 | |||||||
chr11:44172131 | T | A | 1 | a0001c0004t0016g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1305+389T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172131 | |||||||
chr11:44172433 | C | T | 2 | a0001c0002t0004g0041 a0001c0002t0017g0046 |
2 | HG02083.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1305+691C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172433 | |||||||
chr11:44172535 | C | G | 2 | a0001c0001t0009g0267 a0001c0001t0009g0278 |
2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1305+793C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172535 | |||||||
chr11:44172564 | T | A | 1 | a0001c0001t0007g0320 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1305+822T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172564 | |||||||
chr11:44172583 | C | CT | 7 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+858dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44172583 | ||||||
chr11:44172583 | CT | C | 269 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.1305+858delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44172583 | ||||||
chr11:44172592 | T | C | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+850T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172592 | |||||||
chr11:44172605 | T | C | 1 | a0001c0002t0004g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1305+863T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172605 | |||||||
chr11:44172793 | C | T | 1 | a0001c0001t0006g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1305+1051C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172793 | |||||||
chr11:44172862 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1305+1120T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172862 | |||||||
chr11:44172875 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1305+1133C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44172875 | |||||||
chr11:44173077 | C | T | 13 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0001c0001t0011g0310 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1305+1335C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173077 | |||||||
chr11:44173134 | A | G | 109 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(106): Show |
110 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1305+1392A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173134 | |||||||
chr11:44173158 | A | T | 186 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(183): Show |
190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1305+1416A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173158 | |||||||
chr11:44173293 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1305+1551A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173293 | |||||||
chr11:44173332 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+1590G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173332 | |||||||
chr11:44173359 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+1617A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173359 | |||||||
chr11:44173518 | A | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+1776A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173518 | |||||||
chr11:44173563 | C | CT | 11 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(8): Show |
12 | HG02647.hp2 HG04204.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+1844dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44173563 | ||||||
chr11:44173563 | CT | C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(81): Show |
84 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1305+1844delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44173563 | ||||||
chr11:44173566 | T | TC | 6 | a0001c0001t0005g0064 a0001c0001t0014g0298 a0001c0001t0025g0018 others(3): Show |
6 | HG01346.hp1 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+1824_1305+182 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173566 | |||||||
chr11:44173567 | T | C | 185 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(182): Show |
189 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1305+1825T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173567 | |||||||
chr11:44173568 | T | C | 4 | a0001c0001t0002g0180 a0001c0001t0005g0076 a0001c0001t0037g0212 others(1): Show |
4 | HG01081.hp2 HG03017.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+1826T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173568 | |||||||
chr11:44173569 | T | C | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1305+1827T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173569 | |||||||
chr11:44173571 | T | C | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+1829T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173571 | |||||||
chr11:44173599 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+1857C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173599 | |||||||
chr11:44173729 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1305+1987C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173729 | |||||||
chr11:44173741 | T | A | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1305+1999T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173741 | |||||||
chr11:44173758 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2016C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173758 | |||||||
chr11:44173809 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0005g0214 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1305+2067C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173809 | |||||||
chr11:44173908 | T | C | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+2166T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173908 | |||||||
chr11:44173930 | G | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1305+2188G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44173930 | |||||||
chr11:44174025 | A | G | 41 | a0001c0001t0001g0176 a0001c0001t0005g0019 a0001c0001t0005g0062 others(38): Show |
42 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1305+2283A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174025 | |||||||
chr11:44174097 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1305+2355A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174097 | |||||||
chr11:44174152 | A | G | 1 | a0001c0001t0051g0148 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1305+2410A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174152 | |||||||
chr11:44174174 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1305+2432C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174174 | |||||||
chr11:44174336 | C | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2594C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174336 | |||||||
chr11:44174366 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+2624T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174366 | |||||||
chr11:44174410 | T | TTA | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+2684_1305+268 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44174410 | ||||||
chr11:44174414 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+2672A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174414 | |||||||
chr11:44174476 | G | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+2734G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174476 | |||||||
chr11:44174494 | A | G | 2 | a0001c0001t0002g0199 a0001c0001t0002g0200 |
2 | NA18966.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1305+2752A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174494 | |||||||
chr11:44174556 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0001g0129 others(2): Show |
5 | HG00597.hp1 HG00673.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+2814G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174556 | |||||||
chr11:44174568 | C | A | 8 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+2826C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174568 | |||||||
chr11:44174569 | T | C | 186 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(183): Show |
190 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1305+2827T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174569 | |||||||
chr11:44174605 | C | A | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.1305+2863C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174605 | |||||||
chr11:44174707 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+2965C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174707 | |||||||
chr11:44174899 | A | G | 3 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 |
3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1305+3157A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44174899 | |||||||
chr11:44175262 | C | T | 5 | a0001c0001t0010g0194 a0001c0001t0011g0306 a0001c0009t0026g0304 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+3520C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175262 | |||||||
chr11:44175361 | C | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+3619C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175361 | |||||||
chr11:44175376 | C | CT | 16 | a0001c0001t0001g0096 a0001c0001t0001g0275 a0001c0001t0002g0182 others(13): Show |
16 | HG00741.hp1 HG01256.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1305+3642dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44175376 | ||||||
chr11:44175554 | T | G | 1 | a0001c0002t0002g0021 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1305+3812T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44175554 | |||||||
chr11:44176922 | T | TA | 119 | a0001c0001t0001g0099 a0001c0001t0001g0176 a0001c0001t0002g0089 others(116): Show |
121 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1305+5197dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | ||||||
chr11:44176922 | T | TAA | 11 | a0001c0001t0002g0111 a0001c0001t0002g0197 a0001c0001t0002g0198 others(8): Show |
11 | HG00639.hp1 HG01099.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1305+5196_1305+519 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | ||||||
chr11:44176922 | TA | T | 29 | a0001c0001t0003g0227 a0001c0001t0007g0323 a0001c0001t0008g0003 others(26): Show |
30 | HG01109.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.1305+5197delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44176922 | ||||||
chr11:44177025 | A | C | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+5283A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177025 | |||||||
chr11:44177124 | T | C | 2 | a0001c0001t0021g0060 a0001c0001t0021g0061 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1305+5382T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177124 | |||||||
chr11:44177196 | G | A | 1 | a0001c0002t0035g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1305+5454G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177196 | |||||||
chr11:44177312 | T | G | 1 | a0001c0001t0007g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1305+5570T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177312 | |||||||
chr11:44177414 | G | A | 268 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.1305+5672G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177414 | |||||||
chr11:44177449 | C | G | 181 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(178): Show |
185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1305+5707C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177449 | |||||||
chr11:44177526 | G | A | 7 | a0001c0001t0009g0260 a0001c0001t0009g0262 a0001c0001t0009g0264 others(4): Show |
7 | HG00544.hp2 NA18945.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+5784G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177526 | |||||||
chr11:44177722 | G | GT | 180 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(177): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1305+5988dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44177722 | ||||||
chr11:44177722 | GT | G | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+5988delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44177722 | ||||||
chr11:44177730 | T | C | 1 | a0001c0001t0024g0143 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1305+5988T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177730 | |||||||
chr11:44177836 | C | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+6094C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44177836 | |||||||
chr11:44178349 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1305+6607G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178349 | |||||||
chr11:44178419 | G | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+6677G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178419 | |||||||
chr11:44178445 | G | T | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1305+6703G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178445 | |||||||
chr11:44178615 | G | A | 1 | a0001c0001t0006g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1305+6873G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178615 | |||||||
chr11:44178744 | C | G | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+7002C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178744 | |||||||
chr11:44178800 | TA | T | 188 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(185): Show |
193 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1305+7070delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44178800 | ||||||
chr11:44178800 | TAA | T | 12 | a0001c0001t0002g0182 a0001c0001t0022g0327 a0001c0001t0041g0261 others(9): Show |
12 | HG00741.hp1 HG01109.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305+7069_1305+707 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44178800 | ||||||
chr11:44178801 | A | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+7059A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44178801 | |||||||
chr11:44179018 | A | G | 1 | a0001c0001t0013g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1305+7276A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179018 | |||||||
chr11:44179105 | C | G | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+7363C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179105 | |||||||
chr11:44179169 | G | C | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+7427G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179169 | |||||||
chr11:44179296 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1305+7554G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179296 | |||||||
chr11:44179542 | A | G | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1305+7800A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179542 | |||||||
chr11:44179590 | T | C | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1305+7848T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179590 | |||||||
chr11:44179596 | T | C | 1 | a0001c0001t0007g0253 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1305+7854T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179596 | |||||||
chr11:44179680 | A | G | 1 | a0001c0001t0025g0018 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1305+7938A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179680 | |||||||
chr11:44179807 | G | A | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+8065G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44179807 | |||||||
chr11:44180275 | C | T | 1 | a0001c0001t0021g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1305+8533C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180275 | |||||||
chr11:44180439 | A | C | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+8697A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180439 | |||||||
chr11:44180748 | T | C | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1305+9006T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180748 | |||||||
chr11:44180830 | G | A | 1 | a0001c0001t0009g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1305+9088G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180830 | |||||||
chr11:44180867 | C | T | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9125C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180867 | |||||||
chr11:44180877 | G | A | 1 | a0001c0001t0034g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1305+9135G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180877 | |||||||
chr11:44180944 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9202T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44180944 | |||||||
chr11:44181032 | C | T | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9290C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181032 | |||||||
chr11:44181049 | C | T | 54 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(51): Show |
56 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.1305+9307C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181049 | |||||||
chr11:44181057 | C | T | 183 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(180): Show |
187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1305+9315C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181057 | |||||||
chr11:44181100 | CA | C | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1305+9371delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44181100 | ||||||
chr11:44181146 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+9404T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181146 | |||||||
chr11:44181186 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+9444T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181186 | |||||||
chr11:44181348 | G | A | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1305+9606G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181348 | |||||||
chr11:44181461 | G | C | 50 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(47): Show |
52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1305+9719G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181461 | |||||||
chr11:44181501 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+9759C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181501 | |||||||
chr11:44181533 | C | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1305+9791C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181533 | |||||||
chr11:44181547 | G | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1305+9805G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181547 | |||||||
chr11:44181639 | G | T | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+9897G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181639 | |||||||
chr11:44181663 | A | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+9921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181663 | |||||||
chr11:44181789 | A | G | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+10047A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181789 | |||||||
chr11:44181797 | T | C | 1 | a0001c0001t0058g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1305+10055T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44181797 | |||||||
chr11:44182357 | C | A | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0044g0299 |
3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1305+10615C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182357 | |||||||
chr11:44182469 | A | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+10727A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182469 | |||||||
chr11:44182516 | G | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+10774G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182516 | |||||||
chr11:44182609 | G | A | 181 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(178): Show |
185 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.1305+10867G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182609 | |||||||
chr11:44182763 | G | A | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+11021G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182763 | |||||||
chr11:44182973 | A | C | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1305+11231A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44182973 | |||||||
chr11:44183122 | A | G | 1 | a0001c0001t0003g0226 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1305+11380A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183122 | |||||||
chr11:44183161 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1305+11419A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183161 | |||||||
chr11:44183663 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1305+11921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183663 | |||||||
chr11:44183782 | T | A | 1 | a0001c0001t0013g0006 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1305+12040T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183782 | |||||||
chr11:44183802 | G | A | 2 | a0001c0001t0003g0190 a0001c0001t0043g0191 |
2 | HG01361.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1305+12060G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183802 | |||||||
chr11:44183945 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1305+12203T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44183945 | |||||||
chr11:44184082 | G | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1305+12340G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184082 | |||||||
chr11:44184252 | G | C | 96 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(93): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1305+12510G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184252 | |||||||
chr11:44184295 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1305+12553C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184295 | |||||||
chr11:44184296 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1305+12554G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184296 | |||||||
chr11:44184392 | G | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1305+12650G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184392 | |||||||
chr11:44184553 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+12811C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184553 | |||||||
chr11:44184623 | C | T | 1 | a0001c0001t0003g0295 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1305+12881C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184623 | |||||||
chr11:44184758 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1305+13016T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184758 | |||||||
chr11:44184796 | A | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-13033A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44184796 | |||||||
chr11:44185610 | T | C | 1 | a0001c0001t0005g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1306-12219T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185610 | |||||||
chr11:44185671 | C | A | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-12158C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185671 | |||||||
chr11:44185745 | A | T | 40 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(37): Show |
40 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306-12084A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185745 | |||||||
chr11:44185746 | T | C | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-12083T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185746 | |||||||
chr11:44185906 | T | C | 39 | a0001c0001t0001g0176 a0001c0001t0005g0019 a0001c0001t0005g0062 others(36): Show |
40 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1306-11923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185906 | |||||||
chr11:44185958 | A | C | 1 | a0001c0001t0052g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1306-11871A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185958 | |||||||
chr11:44185992 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-11837A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44185992 | |||||||
chr11:44186313 | C | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-11516C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186313 | |||||||
chr11:44186357 | A | G | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1306-11472A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186357 | |||||||
chr11:44186673 | T | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-11156T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186673 | |||||||
chr11:44186790 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-11039C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186790 | |||||||
chr11:44186836 | A | G | 1 | a0001c0001t0042g0279 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1306-10993A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186836 | |||||||
chr11:44186887 | T | C | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1306-10942T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186887 | |||||||
chr11:44186982 | T | TTTCC | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(50): Show |
53 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1306-10786_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | T | TTTCCTTC others(1): Show |
47 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0113 others(44): Show |
49 | HG00323.hp2 HG00544.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306-10790_1306-10 others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | T | TTTCCTTC others(5): Show |
7 | a0001c0001t0006g0136 a0001c0001t0018g0312 a0001c0001t0027g0283 others(4): Show |
7 | HG00639.hp2 HG01109.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306-10794_1306-10 others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | T | TTTCCTTC others(9): Show |
4 | a0001c0001t0006g0164 a0001c0003t0003g0259 a0001c0003t0003g0272 others(1): Show |
4 | HG00438.hp2 HG00544.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-10798_1306-10 others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | T | TTTCCTTC others(13): Show |
1 | a0001c0001t0001g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1306-10802_1306-10 others(26): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | TTTCC | T | 49 | a0001c0001t0002g0179 a0001c0001t0002g0185 a0001c0001t0002g0197 others(46): Show |
49 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1306-10786_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | TTTCCTTC others(1): Show |
T | 71 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(68): Show |
72 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.1306-10790_1306-10 others(14): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | TTTCCTTC others(5): Show |
T | 21 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0184 others(18): Show |
22 | HG00738.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1306-10794_1306-10 others(18): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186982 | TTTCCTTC others(9): Show |
T | 1 | a0001c0002t0004g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1306-10798_1306-10 others(22): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186982 | ||||||
chr11:44186984 | T | TCCTC | 5 | a0001c0001t0011g0306 a0001c0001t0011g0310 a0002c0005t0019g0237 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-10842_1306-10 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44186984 | ||||||
chr11:44186988 | T | C | 4 | a0001c0001t0011g0308 a0001c0001t0011g0309 a0002c0005t0019g0236 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306-10841T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44186988 | |||||||
chr11:44187015 | T | C | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1306-10814T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187015 | |||||||
chr11:44187047 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10782C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187047 | |||||||
chr11:44187051 | T | TTCCCTCC others(8): Show |
1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10770_1306-10 others(21): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44187051 | ||||||
chr11:44187139 | G | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1306-10690G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187139 | |||||||
chr11:44187185 | G | T | 1 | a0001c0001t0014g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1306-10644G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187185 | |||||||
chr11:44187208 | A | T | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-10621A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187208 | |||||||
chr11:44187296 | GCCT | G | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1306-10529_1306-10 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44187296 | ||||||
chr11:44187344 | A | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-10485A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187344 | |||||||
chr11:44187449 | T | C | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1306-10380T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187449 | |||||||
chr11:44187477 | A | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-10352A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187477 | |||||||
chr11:44187521 | T | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1306-10308T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187521 | |||||||
chr11:44187588 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1306-10241T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187588 | |||||||
chr11:44187593 | A | G | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1306-10236A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187593 | |||||||
chr11:44187607 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306-10222T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187607 | |||||||
chr11:44187651 | G | A | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-10178G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187651 | |||||||
chr11:44187755 | G | A | 9 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(6): Show |
9 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-10074G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187755 | |||||||
chr11:44187913 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1306-9916A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44187913 | |||||||
chr11:44188057 | G | T | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-9772G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188057 | |||||||
chr11:44188203 | G | A | 43 | a0001c0001t0004g0325 a0001c0002t0002g0021 a0001c0002t0002g0023 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1306-9626G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188203 | |||||||
chr11:44188213 | A | G | 1 | a0001c0004t0016g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1306-9616A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188213 | |||||||
chr11:44188220 | C | T | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1306-9609C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188220 | |||||||
chr11:44188275 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1306-9554C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188275 | |||||||
chr11:44188301 | G | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-9528G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188301 | |||||||
chr11:44188396 | G | C | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1306-9433G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188396 | |||||||
chr11:44188708 | T | G | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-9121T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44188708 | |||||||
chr11:44189060 | C | T | 3 | a0001c0001t0005g0069 a0001c0001t0005g0070 a0001c0001t0038g0071 |
3 | HG02280.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1306-8769C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189060 | |||||||
chr11:44189089 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1306-8740C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189089 | |||||||
chr11:44189089 | C | T | 182 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(179): Show |
186 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1306-8740C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189089 | |||||||
chr11:44189260 | TAA | T | 3 | a0001c0001t0008g0003 a0001c0001t0008g0244 a0001c0001t0008g0245 |
4 | NA18962.hp2 NA18972.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-8568_1306-856 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189260 | |||||||
chr11:44189466 | G | A | 3 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0039g0174 |
3 | HG03017.hp2 NA18981.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1306-8363G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189466 | |||||||
chr11:44189514 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-8315C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189514 | |||||||
chr11:44189643 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-8186G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189643 | |||||||
chr11:44189714 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1306-8115A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189714 | |||||||
chr11:44189778 | A | G | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1306-8051A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44189778 | |||||||
chr11:44190658 | G | T | 1 | a0001c0002t0004g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1306-7171G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190658 | |||||||
chr11:44190763 | G | A | 8 | a0001c0003t0003g0258 a0001c0003t0003g0259 a0001c0003t0003g0269 others(5): Show |
8 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306-7066G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190763 | |||||||
chr11:44190785 | C | G | 1 | a0003c0006t0055g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1306-7044C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190785 | |||||||
chr11:44190815 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1306-7014G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44190815 | |||||||
chr11:44191208 | G | C | 1 | a0001c0001t0049g0094 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1306-6621G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191208 | |||||||
chr11:44191446 | T | C | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-6383T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191446 | |||||||
chr11:44191667 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1306-6162G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44191667 | |||||||
chr11:44192155 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-5674C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192155 | |||||||
chr11:44192185 | C | T | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-5644C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192185 | |||||||
chr11:44192641 | G | A | 1 | a0001c0001t0022g0327 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306-5188G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192641 | |||||||
chr11:44192857 | T | C | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1306-4972T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192857 | |||||||
chr11:44192858 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1306-4971A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192858 | |||||||
chr11:44192931 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0229 |
2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1306-4898A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192931 | |||||||
chr11:44192963 | G | A | 2 | a0001c0001t0006g0139 a0001c0001t0006g0157 |
2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1306-4866G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44192963 | |||||||
chr11:44193040 | G | C | 1 | a0005c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1306-4789G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193040 | |||||||
chr11:44193114 | T | C | 3 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG00323.hp1 HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1306-4715T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193114 | |||||||
chr11:44193369 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1306-4460G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193369 | |||||||
chr11:44193375 | A | G | 1 | a0001c0001t0010g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1306-4454A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193375 | |||||||
chr11:44193411 | A | C | 1 | a0001c0001t0007g0319 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1306-4418A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193411 | |||||||
chr11:44193605 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1306-4224A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193605 | |||||||
chr11:44193868 | T | C | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.1306-3961T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193868 | |||||||
chr11:44193999 | T | C | 280 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.1306-3830T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44193999 | |||||||
chr11:44194036 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1306-3793G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194036 | |||||||
chr11:44194110 | G | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0296 |
2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1306-3719G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194110 | |||||||
chr11:44194150 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1306-3679G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194150 | |||||||
chr11:44194285 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0027g0284 |
2 | HG02080.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1306-3544G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194285 | |||||||
chr11:44194301 | A | G | 1 | a0001c0001t0005g0019 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1306-3528A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194301 | |||||||
chr11:44194593 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1306-3236C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194593 | |||||||
chr11:44194628 | T | C | 9 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306-3201T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194628 | |||||||
chr11:44194784 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-3045C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44194784 | |||||||
chr11:44195055 | A | G | 4 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0022g0327 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-2774A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195055 | |||||||
chr11:44195157 | G | A | 1 | a0001c0001t0003g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1306-2672G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195157 | |||||||
chr11:44195244 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1306-2585T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195244 | |||||||
chr11:44195423 | ACT | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(82): Show |
85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1306-2403_1306-240 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44195423 | ||||||
chr11:44195432 | C | CA | 8 | a0001c0001t0003g0290 a0001c0004t0016g0172 a0001c0004t0016g0173 others(5): Show |
8 | HG02976.hp1 HG03017.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306-2386dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44195432 | ||||||
chr11:44195460 | C | T | 2 | a0001c0001t0013g0007 a0001c0001t0013g0008 |
2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1306-2369C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195460 | |||||||
chr11:44195584 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1306-2245A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195584 | |||||||
chr11:44195630 | C | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1306-2199C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195630 | |||||||
chr11:44195758 | C | T | 2 | a0001c0001t0005g0074 a0001c0001t0014g0073 |
2 | NA18969.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1306-2071C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195758 | |||||||
chr11:44195798 | T | C | 3 | a0001c0001t0052g0252 a0001c0001t0053g0256 a0001c0014t0061g0238 |
3 | HG02615.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1306-2031T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195798 | |||||||
chr11:44195859 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1306-1970C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195859 | |||||||
chr11:44195947 | C | A | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1306-1882C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44195947 | |||||||
chr11:44196242 | A | T | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-1587A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196242 | |||||||
chr11:44196389 | G | A | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306-1440G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196389 | |||||||
chr11:44196599 | A | AG | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306-1228dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr11 | 44196599 | ||||||
chr11:44196662 | G | A | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306-1167G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44196662 | |||||||
chr11:44197097 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1306-732C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197097 | |||||||
chr11:44197186 | T | C | 3 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 |
3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1306-643T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197186 | |||||||
chr11:44197284 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1306-545G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197284 | |||||||
chr11:44197736 | C | T | 183 | a0001c0001t0001g0013 a0001c0001t0001g0176 a0001c0001t0002g0089 others(180): Show |
187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.1306-93C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 8/13 | chr11 | 44197736 | |||||||
chr11:44198155 | G | A | 4 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+137G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198155 | |||||||
chr11:44198383 | C | CA | 15 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(12): Show |
16 | HG02615.hp2 HG02818.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.1495+377dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44198383 | ||||||
chr11:44198743 | T | C | 1 | a0001c0002t0048g0028 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1495+725T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198743 | |||||||
chr11:44198823 | T | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+805T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198823 | |||||||
chr11:44198885 | C | A | 9 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(6): Show |
10 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.1495+867C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44198885 | |||||||
chr11:44199313 | AAAG | A | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+1299_1495+130 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44199313 | ||||||
chr11:44199477 | T | A | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+1459T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199477 | |||||||
chr11:44199540 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495+1522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199540 | |||||||
chr11:44199691 | G | C | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1495+1673G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199691 | |||||||
chr11:44199725 | A | AT | 115 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(112): Show |
116 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495+1716dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44199725 | ||||||
chr11:44199989 | A | T | 10 | a0001c0001t0008g0003 a0001c0001t0008g0243 a0001c0001t0008g0244 others(7): Show |
11 | HG00544.hp2 HG04204.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495+1971A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44199989 | |||||||
chr11:44200088 | C | G | 9 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495+2070C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200088 | |||||||
chr11:44200151 | T | TA | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+2147dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44200151 | ||||||
chr11:44200152 | A | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(82): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1495+2134A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200152 | |||||||
chr11:44200195 | C | G | 1 | a0001c0002t0008g0054 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1495+2177C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200195 | |||||||
chr11:44200666 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1495+2648C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200666 | |||||||
chr11:44200709 | G | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+2691G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200709 | |||||||
chr11:44200709 | G | T | 1 | a0001c0001t0014g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1495+2691G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200709 | |||||||
chr11:44200726 | T | A | 1 | a0001c0001t0009g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1495+2708T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200726 | |||||||
chr11:44200805 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1495+2787A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200805 | |||||||
chr11:44200866 | A | C | 4 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0022g0327 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+2848A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200866 | |||||||
chr11:44200912 | G | C | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+2894G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44200912 | |||||||
chr11:44201048 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1495+3030A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201048 | |||||||
chr11:44201204 | A | G | 1 | a0005c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1495+3186A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201204 | |||||||
chr11:44201240 | GAC | G | 4 | a0001c0001t0005g0072 a0001c0001t0005g0074 a0001c0001t0014g0073 others(1): Show |
4 | NA18747.hp1 NA18969.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+3226_1495+322 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44201240 | ||||||
chr11:44201273 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1495+3255C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201273 | |||||||
chr11:44201572 | T | C | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1495+3554T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201572 | |||||||
chr11:44201608 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495+3590A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44201608 | |||||||
chr11:44202004 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1495+3986A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202004 | |||||||
chr11:44202072 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1495+4054G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202072 | |||||||
chr11:44202072 | G | C | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1495+4054G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202072 | |||||||
chr11:44202206 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1495+4188C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202206 | |||||||
chr11:44202286 | T | G | 17 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(14): Show |
17 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1495+4268T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202286 | |||||||
chr11:44202306 | T | C | 1 | a0001c0001t0036g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1495+4288T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202306 | |||||||
chr11:44202537 | G | A | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1496-4256G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202537 | |||||||
chr11:44202604 | T | G | 1 | a0001c0001t0011g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1496-4189T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202604 | |||||||
chr11:44202622 | G | T | 1 | a0001c0001t0014g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1496-4171G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44202622 | |||||||
chr11:44203210 | G | C | 176 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(173): Show |
180 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.1496-3583G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203210 | |||||||
chr11:44203267 | C | T | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-3526C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203267 | |||||||
chr11:44203433 | A | G | 2 | a0001c0001t0022g0327 a0001c0001t0022g0328 |
2 | HG01884.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1496-3360A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203433 | |||||||
chr11:44203722 | C | T | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1496-3071C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203722 | |||||||
chr11:44203725 | G | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-3068G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203725 | |||||||
chr11:44203751 | CAGGCACT others(9): Show |
C | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1496-3039_1496-302 others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44203751 | ||||||
chr11:44203773 | T | TAAA | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(85): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1496-3016_1496-301 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44203773 | ||||||
chr11:44203781 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG00735.hp2 HG01175.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496-3012G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203781 | |||||||
chr11:44203810 | C | T | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(85): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1496-2983C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203810 | |||||||
chr11:44203944 | G | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-2849G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44203944 | |||||||
chr11:44204033 | T | G | 40 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(37): Show |
40 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1496-2760T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204033 | |||||||
chr11:44204104 | A | C | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1496-2689A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204104 | |||||||
chr11:44204485 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1496-2308C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204485 | |||||||
chr11:44204499 | G | A | 3 | a0001c0001t0002g0179 a0001c0001t0002g0182 a0001c0001t0002g0185 |
3 | HG00741.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1496-2294G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204499 | |||||||
chr11:44204551 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0050g0103 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1496-2242G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204551 | |||||||
chr11:44204633 | C | T | 190 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(187): Show |
194 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1496-2160C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204633 | |||||||
chr11:44204676 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1496-2117C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44204676 | |||||||
chr11:44205235 | A | G | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1496-1558A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205235 | |||||||
chr11:44205299 | G | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0296 |
2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1496-1494G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205299 | |||||||
chr11:44205359 | A | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1496-1434A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205359 | |||||||
chr11:44205533 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1496-1260A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205533 | |||||||
chr11:44205640 | A | G | 18 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(15): Show |
18 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1496-1153A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205640 | |||||||
chr11:44205726 | G | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1496-1067G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205726 | |||||||
chr11:44205825 | T | A | 1 | a0001c0001t0057g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1496-968T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205825 | |||||||
chr11:44205850 | T | A | 2 | a0001c0001t0003g0293 a0001c0001t0003g0296 |
2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1496-943T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44205850 | |||||||
chr11:44206052 | AAATCCCA others(3): Show |
A | 17 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(14): Show |
17 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1496-737_1496-728d others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44206052 | ||||||
chr11:44206250 | C | T | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-543C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206250 | |||||||
chr11:44206260 | C | A | 10 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(7): Show |
10 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-533C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206260 | |||||||
chr11:44206263 | C | T | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1496-530C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206263 | |||||||
chr11:44206413 | A | G | 2 | a0001c0001t0002g0189 a0004c0012t0002g0186 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1496-380A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206413 | |||||||
chr11:44206429 | T | C | 2 | a0001c0002t0017g0051 a0001c0002t0047g0050 |
2 | HG00621.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1496-364T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206429 | |||||||
chr11:44206564 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1496-229T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206564 | |||||||
chr11:44206572 | GTGTATAT others(4): Show |
G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1496-209_1496-199d others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr11 | 44206572 | ||||||
chr11:44206598 | C | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1496-195C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206598 | |||||||
chr11:44206684 | G | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1496-109G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206684 | |||||||
chr11:44206687 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1496-106G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206687 | |||||||
chr11:44206718 | G | A | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496-75G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 9/13 | chr11 | 44206718 | |||||||
chr11:44207287 | A | G | 1 | a0001c0001t0052g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1662+328A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207287 | |||||||
chr11:44207297 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1662+338C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207297 | |||||||
chr11:44207426 | T | C | 5 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0204 others(2): Show |
5 | HG00639.hp1 HG01099.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+467T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207426 | |||||||
chr11:44207538 | A | T | 1 | a0001c0001t0012g0108 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1662+579A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207538 | |||||||
chr11:44207575 | C | T | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+616C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207575 | |||||||
chr11:44207600 | G | A | 1 | a0001c0001t0027g0284 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1662+641G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207600 | |||||||
chr11:44207808 | T | C | 7 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(4): Show |
7 | HG02559.hp1 HG02976.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+849T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207808 | |||||||
chr11:44207863 | C | G | 1 | a0005c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1662+904C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44207863 | |||||||
chr11:44208098 | C | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+1139C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208098 | |||||||
chr11:44208198 | A | AT | 46 | a0001c0001t0004g0265 a0001c0001t0004g0325 a0001c0001t0027g0283 others(43): Show |
47 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1662+1252dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44208198 | ||||||
chr11:44208312 | G | A | 189 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(186): Show |
193 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1662+1353G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208312 | |||||||
chr11:44208313 | A | G | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+1354A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208313 | |||||||
chr11:44208354 | C | T | 48 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(45): Show |
49 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1662+1395C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208354 | |||||||
chr11:44208551 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1662+1592A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208551 | |||||||
chr11:44208680 | C | T | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1662+1721C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208680 | |||||||
chr11:44208752 | T | C | 193 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(190): Show |
197 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1662+1793T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208752 | |||||||
chr11:44208765 | G | C | 1 | a0001c0001t0036g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1662+1806G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208765 | |||||||
chr11:44208825 | G | A | 1 | a0001c0001t0008g0234 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1662+1866G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208825 | |||||||
chr11:44208825 | G | T | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+1866G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44208825 | |||||||
chr11:44209034 | A | G | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1662+2075A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209034 | |||||||
chr11:44209104 | A | G | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1662+2145A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209104 | |||||||
chr11:44209166 | C | T | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+2207C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209166 | |||||||
chr11:44209209 | G | A | 1 | a0005c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1662+2250G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209209 | |||||||
chr11:44209285 | A | G | 50 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(47): Show |
52 | HG00323.hp2 HG00544.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+2326A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209285 | |||||||
chr11:44209327 | G | A | 1 | a0001c0004t0016g0173 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1662+2368G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209327 | |||||||
chr11:44209448 | A | G | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+2489A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209448 | |||||||
chr11:44209493 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0088 |
3 | HG02258.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1662+2534A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209493 | |||||||
chr11:44209730 | C | T | 5 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(2): Show |
5 | HG00673.hp2 HG02083.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+2771C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209730 | |||||||
chr11:44209802 | C | T | 25 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(22): Show |
25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1662+2843C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209802 | |||||||
chr11:44209966 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+3007A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209966 | |||||||
chr11:44209993 | G | A | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+3034G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44209993 | |||||||
chr11:44210048 | G | A | 1 | a0001c0001t0007g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1662+3089G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210048 | |||||||
chr11:44210183 | A | T | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1662+3224A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210183 | |||||||
chr11:44210191 | G | A | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+3232G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210191 | |||||||
chr11:44210377 | G | A | 1 | a0001c0001t0008g0246 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1662+3418G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210377 | |||||||
chr11:44210569 | G | C | 7 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(4): Show |
7 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+3610G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210569 | |||||||
chr11:44210647 | A | C | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1662+3688A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210647 | |||||||
chr11:44210829 | A | G | 1 | a0001c0001t0011g0309 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1662+3870A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210829 | |||||||
chr11:44210885 | T | C | 199 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(196): Show |
203 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1662+3926T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210885 | |||||||
chr11:44210894 | G | T | 1 | a0003c0006t0055g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1662+3935G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210894 | |||||||
chr11:44210900 | A | T | 1 | a0001c0001t0002g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1662+3941A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44210900 | |||||||
chr11:44211481 | G | A | 5 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(2): Show |
5 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+4522G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211481 | |||||||
chr11:44211570 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0128 |
3 | NA18962.hp1 NA18980.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1662+4611G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211570 | |||||||
chr11:44211633 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1662+4674A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211633 | |||||||
chr11:44211756 | G | C | 4 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0022g0327 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+4797G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211756 | |||||||
chr11:44211845 | T | G | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+4886T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44211845 | |||||||
chr11:44212055 | T | G | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+5096T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212055 | |||||||
chr11:44212154 | A | G | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.1662+5195A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212154 | |||||||
chr11:44212169 | C | A | 3 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 |
3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1662+5210C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212169 | |||||||
chr11:44212260 | G | A | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+5301G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212260 | |||||||
chr11:44212263 | C | T | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+5304C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212263 | |||||||
chr11:44212298 | TATAA | T | 75 | a0001c0001t0003g0231 a0001c0001t0004g0265 a0001c0001t0004g0325 others(72): Show |
76 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1662+5387_1662+539 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | ||||||
chr11:44212298 | TATAAATA others(1): Show |
T | 145 | a0001c0001t0001g0125 a0001c0001t0001g0176 a0001c0001t0002g0089 others(142): Show |
149 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1662+5383_1662+539 others(12): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | ||||||
chr11:44212298 | TATAAATA others(5): Show |
T | 5 | a0001c0001t0002g0233 a0001c0001t0006g0011 a0001c0001t0018g0312 others(2): Show |
5 | HG00639.hp2 HG03834.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+5379_1662+539 others(16): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | ||||||
chr11:44212298 | TATAAATA others(9): Show |
T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1662+5375_1662+539 others(20): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | ||||||
chr11:44212298 | TATAAATA others(13): Show |
T | 5 | a0001c0001t0002g0179 a0001c0001t0002g0182 a0001c0001t0002g0185 others(2): Show |
5 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+5371_1662+539 others(24): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212298 | ||||||
chr11:44212300 | T | A | 6 | a0001c0001t0007g0253 a0001c0001t0009g0266 a0001c0004t0039g0174 others(3): Show |
6 | HG00323.hp2 HG01891.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+5341T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212300 | |||||||
chr11:44212302 | A | C | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1662+5343A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212302 | |||||||
chr11:44212304 | T | A | 62 | a0001c0001t0003g0231 a0001c0001t0004g0265 a0001c0001t0004g0325 others(59): Show |
63 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1662+5345T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212304 | |||||||
chr11:44212306 | AAT | A | 3 | a0001c0001t0003g0303 a0001c0009t0026g0304 a0001c0009t0026g0305 |
3 | HG02896.hp1 HG02970.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1662+5349_1662+535 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44212306 | ||||||
chr11:44212308 | T | A | 127 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(124): Show |
130 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1662+5349T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212308 | |||||||
chr11:44212312 | T | A | 3 | a0001c0001t0002g0233 a0001c0001t0018g0312 a0001c0002t0002g0017 |
3 | HG00639.hp2 HG03834.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1662+5353T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212312 | |||||||
chr11:44212316 | T | A | 3 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0251 |
3 | HG00639.hp1 HG01099.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1662+5357T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212316 | |||||||
chr11:44212320 | T | A | 4 | a0001c0001t0002g0179 a0001c0001t0002g0182 a0001c0001t0002g0185 others(1): Show |
4 | HG00741.hp1 HG01346.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+5361T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212320 | |||||||
chr11:44212407 | C | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+5448C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212407 | |||||||
chr11:44212414 | A | T | 1 | a0001c0001t0003g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1662+5455A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212414 | |||||||
chr11:44212418 | T | C | 97 | a0001c0001t0001g0176 a0001c0001t0003g0190 a0001c0001t0003g0213 others(94): Show |
100 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1662+5459T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212418 | |||||||
chr11:44212497 | G | A | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1662+5538G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212497 | |||||||
chr11:44212660 | T | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+5701T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212660 | |||||||
chr11:44212803 | A | C | 5 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0001g0129 others(2): Show |
5 | HG00597.hp1 HG00673.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+5844A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212803 | |||||||
chr11:44212849 | G | A | 1 | a0001c0002t0004g0044 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1662+5890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44212849 | |||||||
chr11:44213024 | G | T | 2 | a0001c0004t0016g0172 a0001c0004t0016g0173 |
2 | HG03017.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1662+6065G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213024 | |||||||
chr11:44213179 | T | G | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1662+6220T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213179 | |||||||
chr11:44213451 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1662+6492A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213451 | |||||||
chr11:44213469 | A | G | 1 | a0001c0001t0010g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1662+6510A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213469 | |||||||
chr11:44213605 | C | T | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+6646C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213605 | |||||||
chr11:44213703 | C | T | 189 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(186): Show |
193 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1662+6744C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213703 | |||||||
chr11:44213766 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1662+6807T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44213766 | |||||||
chr11:44214042 | T | C | 1 | a0001c0001t0008g0249 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1662+7083T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214042 | |||||||
chr11:44214106 | T | TTTC | 5 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1662+7165_1662+716 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214106 | ||||||
chr11:44214106 | TTTC | T | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1662+7165_1662+716 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214106 | ||||||
chr11:44214150 | G | C | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+7191G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214150 | |||||||
chr11:44214153 | G | A | 35 | a0001c0001t0001g0176 a0001c0001t0005g0019 a0001c0001t0005g0062 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1662+7194G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214153 | |||||||
chr11:44214164 | A | AGTGT | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+7208_1662+720 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214164 | ||||||
chr11:44214176 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+7217C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214176 | |||||||
chr11:44214177 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1662+7218A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214177 | |||||||
chr11:44214300 | G | C | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+7341G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214300 | |||||||
chr11:44214305 | G | C | 1 | a0001c0001t0001g0326 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1662+7346G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214305 | |||||||
chr11:44214327 | C | G | 4 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0022g0327 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+7368C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214327 | |||||||
chr11:44214372 | C | G | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1662+7413C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214372 | |||||||
chr11:44214486 | C | T | 314 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(311): Show |
319 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1662+7527C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214486 | |||||||
chr11:44214751 | C | CT | 20 | a0001c0001t0002g0188 a0001c0001t0008g0003 a0001c0001t0008g0203 others(17): Show |
21 | HG02074.hp1 HG02280.hp1 HG02976.hp1 others(18): Show |
intron_variant | MODIFIER | c.1662+7807dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214751 | ||||||
chr11:44214928 | C | CG | 17 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(14): Show |
18 | HG02027.hp1 HG02074.hp1 HG04204.hp2 others(15): Show |
intron_variant | MODIFIER | c.1662+7975dupG | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44214928 | ||||||
chr11:44214929 | G | A | 2 | a0001c0001t0025g0018 a0001c0001t0025g0083 |
2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1662+7970G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44214929 | |||||||
chr11:44215102 | T | G | 62 | a0001c0001t0001g0112 a0001c0001t0001g0126 a0001c0001t0001g0132 others(59): Show |
63 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1662+8143T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215102 | |||||||
chr11:44215442 | A | G | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+8483A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215442 | |||||||
chr11:44215694 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1662+8735C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215694 | |||||||
chr11:44215716 | AAATTC | A | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1662+8759_1662+876 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215716 | ||||||
chr11:44215865 | A | AT | 11 | a0001c0001t0003g0193 a0001c0001t0007g0321 a0001c0001t0015g0131 others(8): Show |
11 | HG00735.hp1 HG01243.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1662+8928dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | ||||||
chr11:44215865 | AT | A | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1662+8928delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | ||||||
chr11:44215865 | ATTT | A | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+8926_1662+892 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | ||||||
chr11:44215865 | ATTTTTTT others(2): Show |
A | 49 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(46): Show |
51 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1662+8920_1662+892 others(13): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44215865 | ||||||
chr11:44215871 | T | G | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1662+8912T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215871 | |||||||
chr11:44215917 | C | T | 42 | a0001c0001t0004g0265 a0001c0001t0004g0325 a0001c0002t0002g0021 others(39): Show |
43 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1662+8958C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215917 | |||||||
chr11:44215963 | G | A | 133 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(130): Show |
135 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1662+9004G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215963 | |||||||
chr11:44215969 | C | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0296 |
2 | NA18949.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1662+9010C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215969 | |||||||
chr11:44215970 | G | A | 31 | a0001c0001t0003g0190 a0001c0001t0003g0268 a0001c0001t0003g0274 others(28): Show |
33 | HG00544.hp2 HG01109.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1662+9011G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215970 | |||||||
chr11:44215985 | T | C | 1 | a0001c0001t0003g0289 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1662+9026T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44215985 | |||||||
chr11:44216127 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1662+9168C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216127 | |||||||
chr11:44216130 | T | C | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(104): Show |
108 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1662+9171T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216130 | |||||||
chr11:44216490 | A | G | 1 | a0001c0001t0004g0265 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1662+9531A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216490 | |||||||
chr11:44216539 | C | T | 1 | a0001c0001t0031g0217 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1662+9580C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216539 | |||||||
chr11:44216628 | C | T | 136 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(133): Show |
139 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1662+9669C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216628 | |||||||
chr11:44216672 | T | C | 2 | a0001c0001t0052g0252 a0001c0014t0061g0238 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1662+9713T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44216672 | |||||||
chr11:44217175 | A | G | 1 | a0001c0001t0041g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1662+10216A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217175 | |||||||
chr11:44217683 | AT | A | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1662+10734delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44217683 | ||||||
chr11:44217769 | T | A | 2 | a0001c0001t0007g0322 a0001c0001t0007g0323 |
2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1662+10810T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217769 | |||||||
chr11:44217923 | A | T | 2 | a0001c0001t0009g0280 a0001c0001t0042g0279 |
2 | NA19000.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1662+10964A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44217923 | |||||||
chr11:44218051 | C | G | 2 | a0001c0002t0002g0037 a0001c0002t0002g0055 |
2 | NA18954.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1662+11092C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218051 | |||||||
chr11:44218350 | G | T | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1662+11391G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218350 | |||||||
chr11:44218423 | C | T | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1662+11464C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218423 | |||||||
chr11:44218431 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1662+11472C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218431 | |||||||
chr11:44218731 | T | TTTTA | 59 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(56): Show |
61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11772_1662+11 others(10): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218731 | |||||||
chr11:44218732 | A | C | 59 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(56): Show |
61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11773A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218732 | |||||||
chr11:44218733 | A | T | 59 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(56): Show |
61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1662+11774A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218733 | |||||||
chr11:44218749 | A | G | 11 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(8): Show |
11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+11790A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218749 | |||||||
chr11:44218793 | C | CT | 262 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.1662+11856dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | ||||||
chr11:44218793 | C | CTT | 26 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0134 others(23): Show |
26 | HG00673.hp1 HG00741.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1662+11855_1662+11 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | ||||||
chr11:44218793 | C | CTTT | 18 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(15): Show |
19 | HG01978.hp2 HG02300.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1662+11854_1662+11 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44218793 | ||||||
chr11:44218834 | G | T | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+11875G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44218834 | |||||||
chr11:44219096 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1662+12137C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219096 | |||||||
chr11:44219164 | T | C | 1 | a0001c0001t0007g0253 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1662+12205T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219164 | |||||||
chr11:44219215 | C | T | 11 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(8): Show |
11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12256C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219215 | |||||||
chr11:44219229 | C | T | 1 | a0001c0002t0004g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1662+12270C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219229 | |||||||
chr11:44219286 | G | A | 2 | a0001c0001t0009g0267 a0001c0001t0009g0278 |
2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1662+12327G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219286 | |||||||
chr11:44219351 | TA | T | 17 | a0001c0001t0001g0101 a0001c0001t0011g0306 a0001c0001t0011g0308 others(14): Show |
17 | HG00639.hp2 HG01243.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1662+12405delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44219351 | ||||||
chr11:44219406 | C | T | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1662+12447C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219406 | |||||||
chr11:44219527 | A | G | 11 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(8): Show |
11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12568A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219527 | |||||||
chr11:44219620 | T | C | 11 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(8): Show |
11 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1662+12661T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219620 | |||||||
chr11:44219776 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1663-12577C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219776 | |||||||
chr11:44219881 | A | T | 2 | a0001c0001t0008g0244 a0001c0001t0008g0245 |
2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1663-12472A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44219881 | |||||||
chr11:44220236 | C | T | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-12117C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220236 | |||||||
chr11:44220345 | G | A | 2 | a0001c0001t0007g0322 a0001c0001t0007g0323 |
2 | HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1663-12008G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220345 | |||||||
chr11:44220359 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1663-11994G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220359 | |||||||
chr11:44220694 | G | T | 8 | a0001c0001t0004g0265 a0001c0002t0004g0030 a0001c0002t0004g0048 others(5): Show |
8 | HG00621.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1663-11659G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44220694 | |||||||
chr11:44221011 | T | G | 27 | a0001c0001t0005g0005 a0001c0001t0005g0019 a0001c0001t0005g0062 others(24): Show |
28 | HG00099.hp2 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.1663-11342T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221011 | |||||||
chr11:44221063 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1663-11290G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221063 | |||||||
chr11:44221169 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1663-11184G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221169 | |||||||
chr11:44221261 | C | T | 1 | a0001c0001t0007g0175 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1663-11092C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221261 | |||||||
chr11:44221315 | G | A | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-11038G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221315 | |||||||
chr11:44221339 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1663-11014G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221339 | |||||||
chr11:44221660 | C | G | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-10693C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221660 | |||||||
chr11:44221951 | C | G | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0044g0299 |
3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1663-10402C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44221951 | |||||||
chr11:44222001 | A | G | 1 | a0001c0001t0003g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1663-10352A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222001 | |||||||
chr11:44222273 | C | T | 1 | a0001c0007t0005g0147 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1663-10080C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222273 | |||||||
chr11:44222779 | A | T | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-9574A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44222779 | |||||||
chr11:44223127 | A | G | 136 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(133): Show |
139 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1663-9226A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223127 | |||||||
chr11:44223292 | A | G | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-9061A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223292 | |||||||
chr11:44223520 | A | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1663-8833A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223520 | |||||||
chr11:44223641 | A | C | 135 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(132): Show |
138 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1663-8712A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223641 | |||||||
chr11:44223641 | A | G | 1 | a0001c0004t0029g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1663-8712A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223641 | |||||||
chr11:44223642 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1663-8711G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223642 | |||||||
chr11:44223651 | C | CT | 7 | a0001c0001t0001g0149 a0001c0001t0003g0293 a0001c0001t0006g0137 others(4): Show |
7 | HG02572.hp2 HG03831.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-8686dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44223651 | ||||||
chr11:44223672 | C | T | 25 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(22): Show |
25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-8681C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223672 | |||||||
chr11:44223689 | G | A | 2 | a0001c0001t0003g0190 a0001c0001t0043g0191 |
2 | HG01361.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1663-8664G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223689 | |||||||
chr11:44223865 | A | G | 3 | a0001c0001t0013g0006 a0001c0001t0013g0007 a0001c0001t0013g0008 |
3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1663-8488A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223865 | |||||||
chr11:44223898 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0007g0319 |
2 | HG02155.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1663-8455G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223898 | |||||||
chr11:44223930 | A | C | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(313): Show |
intron_variant | MODIFIER | c.1663-8423A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44223930 | |||||||
chr11:44224193 | T | G | 1 | a0001c0001t0036g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-8160T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224193 | |||||||
chr11:44224243 | G | A | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1663-8110G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224243 | |||||||
chr11:44224360 | A | G | 1 | a0001c0001t0036g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-7993A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224360 | |||||||
chr11:44224412 | A | T | 1 | a0002c0005t0019g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1663-7941A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224412 | |||||||
chr11:44224450 | A | G | 6 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-7903A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224450 | |||||||
chr11:44224620 | G | A | 10 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0224 others(7): Show |
10 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1663-7733G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224620 | |||||||
chr11:44224760 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1663-7593G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224760 | |||||||
chr11:44224761 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0154 |
2 | NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1663-7592A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224761 | |||||||
chr11:44224941 | T | G | 1 | a0001c0001t0025g0083 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1663-7412T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224941 | |||||||
chr11:44224949 | A | G | 59 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(56): Show |
61 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1663-7404A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44224949 | |||||||
chr11:44225003 | C | T | 2 | a0001c0001t0021g0060 a0001c0001t0021g0061 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1663-7350C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225003 | |||||||
chr11:44225154 | A | G | 1 | a0001c0001t0007g0322 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1663-7199A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225154 | |||||||
chr11:44225180 | C | A | 47 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(44): Show |
48 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1663-7173C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225180 | |||||||
chr11:44225185 | C | T | 1 | a0001c0001t0004g0325 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1663-7168C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225185 | |||||||
chr11:44225370 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1663-6983T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225370 | |||||||
chr11:44225380 | T | C | 6 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(3): Show |
6 | HG02976.hp1 HG03017.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-6973T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225380 | |||||||
chr11:44225423 | C | G | 1 | a0001c0001t0053g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663-6930C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225423 | |||||||
chr11:44225437 | A | G | 1 | a0001c0002t0004g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1663-6916A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225437 | |||||||
chr11:44225585 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1663-6768C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225585 | |||||||
chr11:44225769 | G | A | 1 | a0001c0004t0039g0174 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1663-6584G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225769 | |||||||
chr11:44225827 | C | T | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1663-6526C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225827 | |||||||
chr11:44225861 | G | T | 1 | a0001c0001t0057g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-6492G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225861 | |||||||
chr11:44225909 | C | A | 1 | a0001c0001t0006g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1663-6444C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44225909 | |||||||
chr11:44226254 | G | A | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-6099G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226254 | |||||||
chr11:44226392 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1663-5961A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226392 | |||||||
chr11:44226420 | T | C | 1 | a0001c0001t0013g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-5933T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226420 | |||||||
chr11:44226665 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1663-5688G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226665 | |||||||
chr11:44226777 | T | C | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1663-5576T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226777 | |||||||
chr11:44226931 | A | G | 3 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0044g0299 |
3 | NA18952.hp1 NA18979.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1663-5422A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44226931 | |||||||
chr11:44227010 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1663-5343C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227010 | |||||||
chr11:44227034 | C | G | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-5319C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227034 | |||||||
chr11:44227072 | C | T | 2 | a0001c0008t0001g0162 a0001c0008t0001g0163 |
2 | HG00438.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1663-5281C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227072 | |||||||
chr11:44227178 | G | T | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1663-5175G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227178 | |||||||
chr11:44227276 | G | C | 199 | a0001c0001t0001g0176 a0001c0001t0002g0089 a0001c0001t0002g0109 others(196): Show |
203 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1663-5077G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227276 | |||||||
chr11:44227314 | A | G | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-5039A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227314 | |||||||
chr11:44227387 | C | G | 15 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(12): Show |
16 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.1663-4966C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227387 | |||||||
chr11:44227432 | A | G | 9 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 others(6): Show |
9 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-4921A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227432 | |||||||
chr11:44227434 | C | T | 25 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(22): Show |
26 | HG00639.hp2 HG01243.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1663-4919C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227434 | |||||||
chr11:44227572 | A | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-4781A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227572 | |||||||
chr11:44227641 | A | T | 1 | a0001c0002t0004g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1663-4712A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227641 | |||||||
chr11:44227683 | G | C | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-4670G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227683 | |||||||
chr11:44227775 | G | A | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-4578G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227775 | |||||||
chr11:44227794 | G | A | 6 | a0001c0002t0004g0001 a0001c0002t0004g0029 a0001c0002t0004g0032 others(3): Show |
7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-4559G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44227794 | |||||||
chr11:44228024 | C | T | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1663-4329C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228024 | |||||||
chr11:44228447 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1663-3906C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228447 | |||||||
chr11:44228448 | G | A | 1 | a0001c0002t0004g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1663-3905G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228448 | |||||||
chr11:44228519 | C | T | 2 | a0001c0001t0002g0196 a0001c0001t0002g0233 |
2 | HG03491.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1663-3834C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228519 | |||||||
chr11:44228541 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1663-3812C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228541 | |||||||
chr11:44228731 | T | C | 311 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(313): Show |
intron_variant | MODIFIER | c.1663-3622T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228731 | |||||||
chr11:44228788 | G | A | 1 | a0001c0001t0003g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1663-3565G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228788 | |||||||
chr11:44228841 | A | C | 1 | a0001c0001t0036g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1663-3512A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228841 | |||||||
chr11:44228855 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1663-3498T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228855 | |||||||
chr11:44228936 | G | T | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1663-3417G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44228936 | |||||||
chr11:44228954 | CAAAGT | C | 37 | a0001c0001t0001g0176 a0001c0001t0005g0019 a0001c0001t0005g0064 others(34): Show |
38 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1663-3395_1663-339 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44228954 | ||||||
chr11:44229070 | G | A | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-3283G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229070 | |||||||
chr11:44229093 | G | A | 2 | a0001c0001t0001g0275 a0001c0013t0001g0087 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1663-3260G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229093 | |||||||
chr11:44229345 | C | T | 57 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(54): Show |
58 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1663-3008C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229345 | |||||||
chr11:44229391 | T | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1663-2962T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229391 | |||||||
chr11:44229559 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1663-2794G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229559 | |||||||
chr11:44229827 | G | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(82): Show |
85 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1663-2526G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229827 | |||||||
chr11:44229986 | A | G | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663-2367A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44229986 | |||||||
chr11:44230221 | G | A | 6 | a0001c0002t0004g0001 a0001c0002t0004g0029 a0001c0002t0004g0032 others(3): Show |
7 | HG00597.hp2 HG02165.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-2132G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230221 | |||||||
chr11:44230286 | A | G | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-2067A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230286 | |||||||
chr11:44230953 | A | G | 41 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(38): Show |
41 | HG00423.hp1 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1663-1400A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230953 | |||||||
chr11:44230982 | G | A | 1 | a0001c0001t0013g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-1371G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44230982 | |||||||
chr11:44231138 | C | G | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1663-1215C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231138 | |||||||
chr11:44231167 | G | T | 47 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(44): Show |
48 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1663-1186G>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231167 | |||||||
chr11:44231253 | C | T | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-1100C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231253 | |||||||
chr11:44231296 | G | A | 1 | a0001c0001t0013g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1663-1057G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231296 | |||||||
chr11:44231408 | G | A | 25 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(22): Show |
25 | HG00423.hp1 HG00639.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-945G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231408 | |||||||
chr11:44231430 | T | C | 2 | a0001c0002t0004g0043 a0001c0002t0004g0044 |
2 | NA19066.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1663-923T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231430 | |||||||
chr11:44231505 | A | G | 2 | a0001c0001t0021g0060 a0001c0001t0021g0061 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1663-848A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231505 | |||||||
chr11:44231787 | A | G | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-566A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231787 | |||||||
chr11:44231853 | G | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1663-500G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231853 | |||||||
chr11:44231917 | C | CT | 17 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(14): Show |
18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-428dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 44231917 | ||||||
chr11:44231925 | T | A | 2 | a0001c0001t0020g0241 a0001c0001t0020g0242 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1663-428T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231925 | |||||||
chr11:44231926 | A | T | 17 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(14): Show |
18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-427A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44231926 | |||||||
chr11:44232038 | G | A | 1 | a0001c0001t0003g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1663-315G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44232038 | |||||||
chr11:44232097 | C | A | 17 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(14): Show |
18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663-256C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 10/13 | chr11 | 44232097 | |||||||
chr11:44232663 | C | T | 1 | a0001c0001t0021g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1806+167C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232663 | |||||||
chr11:44232756 | C | T | 1 | a0001c0001t0010g0059 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1806+260C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232756 | |||||||
chr11:44232790 | G | A | 1 | a0001c0001t0002g0205 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1806+294G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232790 | |||||||
chr11:44232843 | A | G | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1806+347A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232843 | |||||||
chr11:44232915 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1806+419T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232915 | |||||||
chr11:44232936 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1806+440A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44232936 | |||||||
chr11:44233019 | A | T | 3 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0002c0005t0060g0240 |
3 | HG01243.hp1 HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1806+523A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233019 | |||||||
chr11:44233203 | C | T | 9 | a0001c0001t0009g0004 a0001c0001t0009g0257 a0001c0001t0009g0280 others(6): Show |
10 | HG02523.hp2 NA18953.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+707C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233203 | |||||||
chr11:44233225 | T | A | 1 | a0001c0008t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1806+729T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233225 | |||||||
chr11:44233323 | G | C | 2 | a0001c0001t0013g0007 a0001c0001t0013g0008 |
2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1807-792G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233323 | |||||||
chr11:44233324 | A | G | 9 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(6): Show |
9 | HG01891.hp2 HG02976.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-791A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233324 | |||||||
chr11:44233428 | C | G | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1807-687C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233428 | |||||||
chr11:44233430 | C | G | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1807-685C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233430 | |||||||
chr11:44233450 | G | A | 1 | a0001c0004t0059g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1807-665G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233450 | |||||||
chr11:44233530 | G | C | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1807-585G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233530 | |||||||
chr11:44233548 | G | C | 9 | a0001c0004t0016g0172 a0001c0004t0016g0173 a0001c0004t0016g0177 others(6): Show |
9 | HG01891.hp2 HG02976.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1807-567G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233548 | |||||||
chr11:44233587 | A | T | 3 | a0002c0005t0019g0236 a0002c0005t0019g0237 a0002c0005t0019g0239 |
3 | HG01891.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1807-528A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233587 | |||||||
chr11:44233671 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1807-444T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233671 | |||||||
chr11:44233675 | T | C | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1807-440T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233675 | |||||||
chr11:44233933 | C | A | 1 | a0001c0001t0007g0169 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1807-182C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44233933 | |||||||
chr11:44234034 | C | G | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-81C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234034 | |||||||
chr11:44234064 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(87): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1807-51T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234064 | |||||||
chr11:44234086 | A | G | 1 | a0001c0001t0030g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1807-29A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 11/13 | chr11 | 44234086 | |||||||
chr11:44234395 | T | C | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1935+152T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44234395 | |||||||
chr11:44234599 | G | GT | 289 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(286): Show |
293 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.1935+366dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44234599 | ||||||
chr11:44234740 | G | C | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1935+497G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44234740 | |||||||
chr11:44235059 | T | A | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1935+816T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235059 | |||||||
chr11:44235214 | C | G | 1 | a0001c0001t0018g0313 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1935+971C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235214 | |||||||
chr11:44235225 | C | CT | 67 | a0001c0001t0001g0014 a0001c0001t0001g0104 a0001c0001t0001g0126 others(64): Show |
68 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1935+1007dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | ||||||
chr11:44235225 | C | CTT | 80 | a0001c0001t0001g0106 a0001c0001t0002g0089 a0001c0001t0002g0109 others(77): Show |
81 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1935+1006_1935+100 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | ||||||
chr11:44235225 | C | CTTT | 35 | a0001c0001t0001g0105 a0001c0001t0002g0110 a0001c0001t0002g0152 others(32): Show |
35 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1935+1005_1935+100 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | ||||||
chr11:44235225 | CT | C | 12 | a0001c0001t0001g0096 a0001c0001t0007g0169 a0001c0001t0007g0170 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1935+1007delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44235225 | ||||||
chr11:44235250 | T | TTTG | 21 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(18): Show |
23 | HG00544.hp2 HG01099.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(7): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | |||||||
chr11:44235250 | T | TTTTG | 22 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0003g0228 others(19): Show |
22 | HG01109.hp1 HG01175.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(8): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | |||||||
chr11:44235250 | T | TTTTTG | 7 | a0001c0001t0003g0193 a0001c0001t0003g0220 a0001c0001t0003g0226 others(4): Show |
7 | HG01243.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+1007_1935+100 others(9): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235250 | |||||||
chr11:44235303 | C | T | 46 | a0001c0001t0003g0190 a0001c0001t0003g0213 a0001c0001t0003g0230 others(43): Show |
47 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1936-990C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235303 | |||||||
chr11:44235390 | C | T | 136 | a0001c0001t0002g0089 a0001c0001t0002g0109 a0001c0001t0002g0110 others(133): Show |
138 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.1936-903C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235390 | |||||||
chr11:44235398 | T | C | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.1936-895T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235398 | |||||||
chr11:44235403 | G | A | 1 | a0001c0001t0003g0303 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1936-890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235403 | |||||||
chr11:44235421 | A | G | 4 | a0001c0002t0004g0001 a0001c0002t0004g0033 a0001c0002t0004g0057 others(1): Show |
5 | HG00597.hp2 NA18984.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-872A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235421 | |||||||
chr11:44235463 | C | A | 1 | a0005c0011t0008g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1936-830C>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235463 | |||||||
chr11:44235610 | T | A | 2 | a0001c0001t0005g0005 a0001c0001t0005g0281 |
3 | HG01255.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1936-683T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235610 | |||||||
chr11:44235872 | G | A | 1 | a0001c0001t0023g0254 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1936-421G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235872 | |||||||
chr11:44235906 | G | A | 1 | a0001c0001t0005g0062 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1936-387G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235906 | |||||||
chr11:44235979 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1936-314A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44235979 | |||||||
chr11:44236119 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1936-174G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236119 | |||||||
chr11:44236158 | G | GGT | 3 | a0001c0001t0005g0062 a0001c0001t0005g0076 a0001c0001t0046g0311 |
3 | HG03471.hp1 NA18977.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1936-117_1936-116d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44236158 | ||||||
chr11:44236158 | GGT | G | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.1936-117_1936-116d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 44236158 | ||||||
chr11:44236180 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1936-113C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236180 | |||||||
chr11:44236227 | G | C | 18 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(15): Show |
19 | HG01243.hp1 HG04204.hp2 NA18522.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936-66G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236227 | |||||||
chr11:44236252 | T | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1936-41T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 12/13 | chr11 | 44236252 | |||||||
chr11:44236825 | G | A | 1 | a0001c0001t0052g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2018+450G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44236825 | |||||||
chr11:44236985 | G | A | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+610G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44236985 | |||||||
chr11:44237027 | A | G | 1 | a0001c0001t0006g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2018+652A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237027 | |||||||
chr11:44237174 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2018+799G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237174 | |||||||
chr11:44237227 | A | G | 1 | a0001c0002t0004g0052 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2018+852A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237227 | |||||||
chr11:44237277 | T | TTG | 3 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG00323.hp1 HG01168.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2018+913_2018+914d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237277 | ||||||
chr11:44237287 | G | C | 1 | a0001c0001t0003g0291 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2018+912G>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237287 | |||||||
chr11:44237439 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+1064T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237439 | |||||||
chr11:44237739 | A | G | 3 | a0001c0001t0018g0312 a0001c0001t0018g0313 a0001c0001t0018g0314 |
3 | HG00639.hp2 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2018+1364A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237739 | |||||||
chr11:44237858 | G | A | 1 | a0001c0002t0004g0020 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2018+1483G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237858 | |||||||
chr11:44237902 | T | TA | 50 | a0001c0001t0002g0110 a0001c0001t0002g0179 a0001c0001t0002g0180 others(47): Show |
50 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2018+1555dupA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237902 | ||||||
chr11:44237902 | TA | T | 58 | a0001c0001t0002g0196 a0001c0001t0002g0233 a0001c0001t0003g0190 others(55): Show |
60 | HG00544.hp2 HG00639.hp2 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.2018+1555delA | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44237902 | ||||||
chr11:44237919 | A | AC | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(79): Show |
82 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2018+1544_2018+154 others(5): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237919 | |||||||
chr11:44237920 | A | C | 1 | a0001c0002t0004g0040 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2018+1545A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237920 | |||||||
chr11:44237942 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0154 |
2 | NA18943.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2018+1567A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44237942 | |||||||
chr11:44238053 | C | T | 56 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0213 others(53): Show |
57 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.2018+1678C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238053 | |||||||
chr11:44238275 | T | G | 1 | a0001c0001t0007g0324 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2018+1900T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238275 | |||||||
chr11:44238592 | A | G | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2018+2217A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238592 | |||||||
chr11:44238606 | G | A | 7 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(4): Show |
7 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018+2231G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238606 | |||||||
chr11:44238707 | T | C | 2 | a0001c0001t0005g0069 a0001c0001t0005g0070 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2018+2332T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238707 | |||||||
chr11:44238884 | A | G | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.2018+2509A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238884 | |||||||
chr11:44238899 | A | G | 1 | a0001c0009t0026g0305 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2018+2524A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44238899 | |||||||
chr11:44239003 | G | A | 2 | a0001c0001t0002g0189 a0004c0012t0002g0186 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2018+2628G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239003 | |||||||
chr11:44239092 | A | C | 1 | a0001c0001t0028g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2018+2717A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239092 | |||||||
chr11:44239235 | T | A | 1 | a0001c0001t0038g0071 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2018+2860T>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239235 | |||||||
chr11:44239254 | G | A | 35 | a0001c0001t0005g0019 a0001c0001t0005g0062 a0001c0001t0005g0064 others(32): Show |
36 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2018+2879G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239254 | |||||||
chr11:44239298 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2018+2923C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239298 | |||||||
chr11:44239393 | C | CT | 276 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(273): Show |
281 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.2018+3036dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239393 | ||||||
chr11:44239393 | C | CTT | 13 | a0001c0001t0001g0178 a0001c0001t0001g0275 a0001c0001t0002g0109 others(10): Show |
13 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2018+3035_2018+303 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239393 | ||||||
chr11:44239427 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2018+3052T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239427 | |||||||
chr11:44239517 | C | T | 1 | a0001c0001t0005g0074 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2018+3142C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239517 | |||||||
chr11:44239633 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2018+3258C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239633 | |||||||
chr11:44239642 | C | T | 1 | a0001c0001t0046g0311 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2018+3267C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239642 | |||||||
chr11:44239689 | C | CT | 30 | a0001c0001t0001g0010 a0001c0001t0001g0098 a0001c0001t0001g0114 others(27): Show |
30 | HG00597.hp1 HG00639.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.2018+3340dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | ||||||
chr11:44239689 | CT | C | 78 | a0001c0001t0001g0113 a0001c0001t0002g0109 a0001c0001t0002g0110 others(75): Show |
79 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2018+3340delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | ||||||
chr11:44239689 | CTT | C | 11 | a0001c0001t0020g0241 a0001c0001t0020g0242 a0001c0001t0028g0329 others(8): Show |
11 | HG01243.hp1 HG01993.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2018+3339_2018+334 others(6): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | ||||||
chr11:44239689 | CTTTTTTT others(4): Show |
C | 40 | a0001c0001t0005g0005 a0001c0001t0005g0019 a0001c0001t0005g0062 others(37): Show |
42 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2018+3330_2018+334 others(15): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44239689 | ||||||
chr11:44239820 | A | T | 17 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(14): Show |
18 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.2018+3445A>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239820 | |||||||
chr11:44239906 | C | T | 3 | a0001c0007t0005g0147 a0001c0007t0005g0221 a0001c0007t0005g0232 |
3 | HG02818.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2018+3531C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44239906 | |||||||
chr11:44240019 | A | G | 2 | a0001c0001t0009g0267 a0001c0001t0009g0278 |
2 | NA18945.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2018+3644A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240019 | |||||||
chr11:44240020 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2018+3645T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240020 | |||||||
chr11:44240305 | G | A | 1 | a0001c0001t0041g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2019-3844G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240305 | |||||||
chr11:44240878 | C | G | 4 | a0001c0001t0015g0131 a0001c0001t0015g0219 a0001c0001t0015g0222 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2019-3271C>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240878 | |||||||
chr11:44240879 | T | C | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2019-3270T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44240879 | |||||||
chr11:44241131 | A | G | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.2019-3018A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241131 | |||||||
chr11:44241249 | G | A | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-2900G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241249 | |||||||
chr11:44241259 | G | A | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.2019-2890G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241259 | |||||||
chr11:44241326 | A | C | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG04204.hp2 NA18945.hp1 NA18954.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-2823A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241326 | |||||||
chr11:44241687 | A | G | 30 | a0001c0001t0004g0265 a0001c0001t0004g0325 a0001c0002t0004g0001 others(27): Show |
31 | HG00438.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2019-2462A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44241687 | |||||||
chr11:44242055 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2019-2094G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242055 | |||||||
chr11:44242149 | G | A | 5 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0001t0007g0175 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-2000G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242149 | |||||||
chr11:44242237 | T | C | 1 | a0001c0002t0035g0047 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2019-1912T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242237 | |||||||
chr11:44242298 | C | T | 3 | a0001c0001t0027g0283 a0001c0001t0027g0284 a0001c0001t0062g0285 |
3 | HG02622.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2019-1851C>T | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242298 | |||||||
chr11:44242349 | A | C | 3 | a0001c0001t0013g0006 a0001c0001t0013g0007 a0001c0001t0013g0008 |
3 | HG01123.hp2 HG02615.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2019-1800A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242349 | |||||||
chr11:44242782 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2019-1367T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242782 | |||||||
chr11:44242948 | A | G | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(84): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2019-1201A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44242948 | |||||||
chr11:44243045 | A | C | 26 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(23): Show |
27 | HG00639.hp2 HG01243.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.2019-1104A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243045 | |||||||
chr11:44243097 | A | G | 16 | a0001c0001t0008g0003 a0001c0001t0008g0203 a0001c0001t0008g0234 others(13): Show |
17 | HG02074.hp1 HG04204.hp2 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.2019-1052A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243097 | |||||||
chr11:44243158 | G | A | 5 | a0001c0001t0011g0306 a0001c0001t0011g0308 a0001c0001t0011g0309 others(2): Show |
5 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2019-991G>A | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243158 | |||||||
chr11:44243238 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-911T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243238 | |||||||
chr11:44243349 | A | G | 313 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(315): Show |
intron_variant | MODIFIER | c.2019-800A>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243349 | |||||||
chr11:44243412 | A | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-737A>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243412 | |||||||
chr11:44243498 | T | G | 1 | a0006c0010t0011g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2019-651T>G | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243498 | |||||||
chr11:44243562 | T | C | 325 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.2019-587T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44243562 | |||||||
chr11:44243618 | C | CT | 19 | a0001c0001t0001g0088 a0001c0001t0001g0155 a0001c0001t0003g0293 others(16): Show |
19 | HG00735.hp1 HG01099.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2019-506dupT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | ||||||
chr11:44243618 | C | CTT | 18 | a0001c0001t0001g0133 a0001c0001t0008g0003 a0001c0001t0008g0203 others(15): Show |
19 | HG00609.hp2 HG02074.hp1 HG04204.hp2 others(16): Show |
intron_variant | MODIFIER | c.2019-507_2019-506d others(4): Show |
EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | ||||||
chr11:44243618 | CT | C | 76 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0218 others(73): Show |
77 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.2019-506delT | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr11 | 44243618 | ||||||
chr11:44244065 | T | C | 2 | a0001c0009t0026g0304 a0001c0009t0026g0305 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2019-84T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44244065 | |||||||
chr11:44244135 | T | C | 1 | a0002c0005t0060g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2019-14T>C | EXT2 | ENSG00000151348.16 | transcript | ENST00000533608.7 | protein_coding | 13/13 | chr11 | 44244135 |