Item | Value |
---|---|
geneid | 119710 |
ensemblid | ENSG00000166352.18 |
hgncid | 25142 |
symbol | IFTAP |
name | intraflagellar transport associated protein |
refseq_nuc | NM_138787.4 |
refseq_prot | NP_620142.2 |
ensembl_nuc | ENST00000334307.10 |
ensembl_prot | ENSP00000334848.5 |
mane_status | MANE Select |
chr | chr11 |
start | 36594502 |
end | 36659272 |
strand | + |
ver | v1.2 |
region | chr11:36594502-36659272 |
region5000 | chr11:36589502-36664272 |
regionname0 | IFTAP_chr11_36594502_36659272 |
regionname5000 | IFTAP_chr11_36589502_36664272 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 221 | 351 | 89 | 67 | 150 | 12 | 31 | 112 | IFTAP_chr11_36589502_36664272 | IFTAP | MSAHM others(216): Show |
chr11 | 36589502 | 36664272 |
a0002 | 0/0 | 221 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | MSAHM others(216): Show |
chr11 | 36589502 | 36664272 |
a0003 | 0/0 | 221 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | MSAHM others(216): Show |
chr11 | 36589502 | 36664272 |
a0004 | 0/0 | 221 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | MSAHM others(216): Show |
chr11 | 36589502 | 36664272 |
a0005 | 0/0 | 221 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | MSAHM others(216): Show |
chr11 | 36589502 | 36664272 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 663 | 345 | 83 | 67 | 150 | 12 | 31 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0001c0002 | 0/0 | 663 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0002c0003 | 0/0 | 663 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0002c0004 | 0/0 | 663 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0003c0006 | 0/0 | 663 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0004c0007 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 | ||
a0005c0005 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | ATGTC others(658): Show |
chr11 | 36589502 | 36664272 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 866 | 295 | 61 | 57 | 138 | 8 | 29 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0001c0001t0002 | 0/0 | 866 | 48 | 22 | 10 | 12 | 3 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0001c0001t0004 | 0/0 | 866 | 2 | 0 | 0 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0001c0002t0003 | 0/0 | 866 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0002c0003t0002 | 0/0 | 866 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0002c0004t0002 | 0/0 | 866 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0003c0006t0001 | 0/0 | 866 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0004c0007t0001 | 0/0 | 866 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
a0005c0005t0002 | 0/0 | 866 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | CTCTC others(861): Show |
chr11 | 36589502 | 36664272 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 3 | 0 | 11 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 3 | 8 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0004 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0007 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0003t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0004t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0003c0006t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0004c0007t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0005c0005t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0235 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01243 | hp2 | a0003 | c0006 | t0001 | g0059 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01891 | hp2 | a0004 | c0007 | t0001 | g0118 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02615 | hp2 | a0002 | c0004 | t0002 | g0230 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0205 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03195 | hp1 | a0002 | c0004 | t0002 | g0014 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03239 | hp1 | a0005 | c0005 | t0002 | g0016 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0203 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0204 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | TSI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0195 | REF | REF | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0080 | REF | REF | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36610161 | G | A | 1 | a0002 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.58G>A | p.Val20Ile | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 172/866 | 58/666 | 20/221 | chr11 | 36610161 | |||
chr11:36610171 | A | T | 1 | a0004 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.68A>T | p.Lys23Ile | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 182/866 | 68/666 | 23/221 | chr11 | 36610171 | |||
chr11:36633338 | T | C | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.191T>C | p.Phe64Ser | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/6 | 305/866 | 191/666 | 64/221 | chr11 | 36633338 | |||
chr11:36659169 | G | A | 1 | a0003 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.649G>A | p.Glu217Lys | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 6/6 | 763/866 | 649/666 | 217/221 | chr11 | 36659169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36610160 | C | T | 1 | a0001c0002 | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
synonymous_variant | LOW | c.57C>T | p.Asp19Asp | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 171/866 | 57/666 | 19/221 | chr11 | 36610160 | |||
chr11:36633354 | T | C | 1 | a0002c0003 | 2 | HG02970.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.207T>C | p.Val69Val | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/6 | 321/866 | 207/666 | 69/221 | chr11 | 36633354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36594508 | G | C | 1 | a0001c0002t0003 | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-108G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/6 | 15596 | chr11 | 36594508 | ||||||
chr11:36594562 | G | C | 5 | a0001c0001t0002 a0001c0002t0003 a0002c0003t0002 others(2): Show |
59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-54G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/6 | 15542 | chr11 | 36594562 | ||||||
chr11:36659215 | T | C | 1 | a0001c0001t0004 | 2 | HG00140.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 6/6 | 29 | chr11 | 36659215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36595200 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+608G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595200 | |||||||
chr11:36595228 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0038 others(32): Show |
59 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-24+636C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595228 | |||||||
chr11:36595234 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-24+642A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595234 | |||||||
chr11:36595317 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
172 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.-24+725A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595317 | |||||||
chr11:36595455 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-24+863G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595455 | |||||||
chr11:36595503 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+911A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595503 | |||||||
chr11:36595597 | T | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1005T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595597 | |||||||
chr11:36595644 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+1052T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595644 | |||||||
chr11:36595718 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1126G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595718 | |||||||
chr11:36595754 | C | T | 15 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(12): Show |
16 | HG00438.hp1 HG02523.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24+1162C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595754 | |||||||
chr11:36595761 | T | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0229 others(3): Show |
7 | HG02615.hp2 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+1169T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595761 | |||||||
chr11:36595789 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-24+1197A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595789 | |||||||
chr11:36595804 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24+1212C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595804 | |||||||
chr11:36595945 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-24+1353A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595945 | |||||||
chr11:36596026 | A | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0209 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-24+1434A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596026 | |||||||
chr11:36596065 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-24+1473C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596065 | |||||||
chr11:36596211 | G | GT | 6 | a0001c0001t0002g0032 a0001c0001t0002g0210 a0001c0001t0002g0211 others(3): Show |
7 | HG01496.hp1 HG01517.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+1629dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | ||||||
chr11:36596211 | G | GTT | 12 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
15 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+1628_-24+1629d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | ||||||
chr11:36596211 | G | GTTT | 11 | a0001c0001t0001g0031 a0001c0001t0001g0200 a0001c0001t0002g0036 others(8): Show |
13 | HG01106.hp2 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24+1627_-24+1629d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | ||||||
chr11:36596211 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+1629_-24+1630i others(18): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | ||||||
chr11:36596218 | TTTTG | T | 10 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(7): Show |
10 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+1630_-24+1633d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596218 | ||||||
chr11:36596222 | G | GT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
109 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-24+1645dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596222 | ||||||
chr11:36596222 | G | GTT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0137 a0001c0001t0001g0174 others(8): Show |
12 | HG01074.hp2 HG01192.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24+1644_-24+1645d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596222 | ||||||
chr11:36596222 | G | T | 33 | a0001c0001t0001g0031 a0001c0001t0001g0196 a0001c0001t0001g0197 others(30): Show |
39 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24+1630G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596222 | |||||||
chr11:36596233 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-24+1641T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596233 | |||||||
chr11:36596260 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-24+1668C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596260 | |||||||
chr11:36596265 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1673G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596265 | |||||||
chr11:36596308 | C | A | 2 | a0001c0001t0004g0234 a0001c0001t0004g0235 |
2 | HG00140.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-24+1716C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596308 | |||||||
chr11:36596323 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+1731G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596323 | |||||||
chr11:36596333 | G | T | 1 | a0001c0001t0001g0048 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+1741G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596333 | |||||||
chr11:36596439 | T | C | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+1847T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596439 | |||||||
chr11:36596446 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-24+1854C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596446 | |||||||
chr11:36596475 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+1883G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596475 | |||||||
chr11:36596695 | C | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2103C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596695 | |||||||
chr11:36596713 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0192 a0001c0001t0001g0193 |
5 | HG00438.hp2 NA18944.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+2121A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596713 | |||||||
chr11:36596839 | G | T | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+2247G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596839 | |||||||
chr11:36596904 | A | G | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+2312A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596904 | |||||||
chr11:36596999 | T | A | 1 | a0003c0006t0001g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24+2407T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596999 | |||||||
chr11:36597100 | A | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2508A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597100 | |||||||
chr11:36597125 | A | G | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+2533A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597125 | |||||||
chr11:36597333 | A | C | 28 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(25): Show |
34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-24+2741A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597333 | |||||||
chr11:36597633 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+3041C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597633 | |||||||
chr11:36597694 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-24+3102G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597694 | |||||||
chr11:36597744 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+3152G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597744 | |||||||
chr11:36597745 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-24+3153G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597745 | |||||||
chr11:36597754 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0219 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+3162G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597754 | |||||||
chr11:36597834 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-24+3242T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597834 | |||||||
chr11:36597876 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24+3284C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597876 | |||||||
chr11:36597917 | C | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+3325C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597917 | |||||||
chr11:36597938 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+3346G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597938 | |||||||
chr11:36598211 | A | G | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+3619A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598211 | |||||||
chr11:36598299 | CT | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+3716delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36598299 | ||||||
chr11:36598542 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
168 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.-24+3950G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598542 | |||||||
chr11:36598545 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-24+3953G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598545 | |||||||
chr11:36598677 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24+4085C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598677 | |||||||
chr11:36598742 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
10 | HG00544.hp1 HG01934.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+4150G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598742 | |||||||
chr11:36598837 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-24+4245T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598837 | |||||||
chr11:36598852 | C | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-24+4260C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598852 | |||||||
chr11:36599108 | C | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-24+4516C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599108 | |||||||
chr11:36599215 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+4623A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599215 | |||||||
chr11:36599539 | A | G | 1 | a0001c0002t0003g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-24+4947A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599539 | |||||||
chr11:36599570 | C | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+4978C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599570 | |||||||
chr11:36599642 | A | AT | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5059dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36599642 | ||||||
chr11:36599642 | AT | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
7 | HG00609.hp1 HG00673.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+5059delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36599642 | ||||||
chr11:36599705 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
10 | HG00544.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+5113G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599705 | |||||||
chr11:36599806 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-24+5214T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599806 | |||||||
chr11:36599883 | A | G | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+5291A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599883 | |||||||
chr11:36599884 | T | C | 4 | a0001c0001t0002g0049 a0002c0003t0002g0014 a0002c0004t0002g0014 others(1): Show |
5 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+5292T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599884 | |||||||
chr11:36600009 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-24+5417A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600009 | |||||||
chr11:36600045 | A | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+5453A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600045 | |||||||
chr11:36600216 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-24+5624A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600216 | |||||||
chr11:36600232 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-24+5640G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600232 | |||||||
chr11:36600237 | A | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
10 | HG00544.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+5645A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600237 | |||||||
chr11:36600308 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+5716A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600308 | |||||||
chr11:36600362 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+5770C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600362 | |||||||
chr11:36600406 | A | G | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+5814A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600406 | |||||||
chr11:36600411 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-24+5819G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600411 | |||||||
chr11:36600412 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-24+5820C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600412 | |||||||
chr11:36600476 | A | C | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+5884A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600476 | |||||||
chr11:36600477 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5885G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600477 | |||||||
chr11:36600519 | C | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5927C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600519 | |||||||
chr11:36600564 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-24+5972T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600564 | |||||||
chr11:36600578 | A | G | 10 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0229 others(7): Show |
13 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24+5986A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600578 | |||||||
chr11:36600624 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-24+6032C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600624 | |||||||
chr11:36600921 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(193): Show |
271 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.-24+6329C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600921 | |||||||
chr11:36601043 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+6451C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601043 | |||||||
chr11:36601252 | G | A | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+6660G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601252 | |||||||
chr11:36601504 | G | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+6912G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601504 | |||||||
chr11:36601751 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+7159C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601751 | |||||||
chr11:36601758 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-24+7166A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601758 | |||||||
chr11:36601810 | T | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0236 |
5 | HG01243.hp1 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+7218T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601810 | |||||||
chr11:36601828 | A | AT | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+7242dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36601828 | ||||||
chr11:36601966 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+7374A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601966 | |||||||
chr11:36602108 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-24+7516A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602108 | |||||||
chr11:36602143 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-24+7551A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602143 | |||||||
chr11:36602461 | T | G | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-23-7620T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602461 | |||||||
chr11:36602513 | A | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-7568A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602513 | |||||||
chr11:36602523 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-23-7558G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602523 | |||||||
chr11:36602576 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-23-7505G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602576 | |||||||
chr11:36602633 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-7448C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602633 | |||||||
chr11:36602637 | G | A | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-7444G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602637 | |||||||
chr11:36602831 | TA | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-23-7240delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36602831 | ||||||
chr11:36602890 | T | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7191T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602890 | |||||||
chr11:36603024 | A | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-7057A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603024 | |||||||
chr11:36603489 | C | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-6592C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603489 | |||||||
chr11:36603511 | T | G | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-23-6570T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603511 | |||||||
chr11:36603566 | A | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6515A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603566 | |||||||
chr11:36603645 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0237 |
5 | HG02129.hp1 NA18961.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-6436G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603645 | |||||||
chr11:36603696 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0253 others(1): Show |
7 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-6385C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603696 | |||||||
chr11:36603722 | G | T | 4 | a0001c0001t0002g0229 a0002c0003t0002g0014 a0002c0004t0002g0014 others(1): Show |
5 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-6359G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603722 | |||||||
chr11:36603802 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-23-6279A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603802 | |||||||
chr11:36603922 | CA | C | 11 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG00621.hp1 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23-6144delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36603922 | ||||||
chr11:36603922 | CAAA | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6146_-23-6144d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36603922 | ||||||
chr11:36603954 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-6127T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603954 | |||||||
chr11:36603981 | C | G | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6100C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603981 | |||||||
chr11:36603994 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-23-6087G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603994 | |||||||
chr11:36604054 | T | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-6027T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604054 | |||||||
chr11:36604077 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-6004T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604077 | |||||||
chr11:36604155 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-23-5926A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604155 | |||||||
chr11:36604230 | T | TAATATTC others(354): Show |
1 | a0001c0001t0002g0226 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-23-5838_-23-5837i others(363): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604230 | ||||||
chr11:36604230 | T | TAATATTC others(355): Show |
2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-5838_-23-5837i others(364): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604230 | ||||||
chr11:36604246 | G | A | 28 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(25): Show |
34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-23-5835G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604246 | |||||||
chr11:36604396 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-23-5685A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604396 | |||||||
chr11:36604629 | A | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-5452A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604629 | |||||||
chr11:36604672 | T | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-5409T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604672 | |||||||
chr11:36604685 | C | T | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0189 others(2): Show |
5 | HG01358.hp2 HG01516.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-5396C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604685 | |||||||
chr11:36604707 | A | T | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-5374A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604707 | |||||||
chr11:36604725 | C | CT | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01981.hp1 HG02080.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-5355dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604725 | ||||||
chr11:36604894 | C | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-23-5187C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604894 | |||||||
chr11:36604930 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-23-5151A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604930 | |||||||
chr11:36605032 | G | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23-5049G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605032 | |||||||
chr11:36605055 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-5026A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605055 | |||||||
chr11:36605090 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0201 others(9): Show |
15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-4991C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605090 | |||||||
chr11:36605211 | T | A | 51 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(48): Show |
60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-23-4870T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605211 | |||||||
chr11:36605287 | C | A | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-4794C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605287 | |||||||
chr11:36605289 | CT | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4781delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36605289 | ||||||
chr11:36605309 | A | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-4772A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605309 | |||||||
chr11:36605588 | A | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4493A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605588 | |||||||
chr11:36605643 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4438A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605643 | |||||||
chr11:36605671 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-23-4410T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605671 | |||||||
chr11:36605672 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-23-4409G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605672 | |||||||
chr11:36605807 | A | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-4274A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605807 | |||||||
chr11:36605891 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23-4190C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605891 | |||||||
chr11:36605919 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4162G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605919 | |||||||
chr11:36606000 | C | T | 1 | a0001c0001t0001g0030 | 2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-23-4081C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606000 | |||||||
chr11:36606003 | T | C | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-4078T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606003 | |||||||
chr11:36606006 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-23-4075G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606006 | |||||||
chr11:36606011 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-23-4070C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606011 | |||||||
chr11:36606257 | G | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-3824G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606257 | |||||||
chr11:36606304 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-23-3777C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606304 | |||||||
chr11:36606441 | C | CTAAA | 38 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(35): Show |
43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-23-3621_-23-3618d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606441 | ||||||
chr11:36606485 | CTA | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3592_-23-3591d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606485 | ||||||
chr11:36606625 | GA | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3452delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606625 | ||||||
chr11:36606690 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-23-3391T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606690 | |||||||
chr11:36606824 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-23-3257C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606824 | |||||||
chr11:36606963 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-3118A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606963 | |||||||
chr11:36606990 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3091A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606990 | |||||||
chr11:36606991 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-3090G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606991 | |||||||
chr11:36607001 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3080G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607001 | |||||||
chr11:36607054 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-3027A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607054 | |||||||
chr11:36607059 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3022A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607059 | |||||||
chr11:36607283 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-2798G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607283 | |||||||
chr11:36607288 | C | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-2793C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607288 | |||||||
chr11:36607350 | T | A | 27 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-23-2731T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607350 | |||||||
chr11:36607528 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-23-2553A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607528 | |||||||
chr11:36607593 | AT | A | 14 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23-2477delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36607593 | ||||||
chr11:36607665 | T | TC | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-2410dupC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36607665 | ||||||
chr11:36607736 | T | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-2345T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607736 | |||||||
chr11:36607751 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23-2330G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607751 | |||||||
chr11:36607754 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-23-2327A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607754 | |||||||
chr11:36607818 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-23-2263C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607818 | |||||||
chr11:36608064 | G | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | NA18961.hp1 NA18970.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-2017G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608064 | |||||||
chr11:36608477 | T | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-1604T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608477 | |||||||
chr11:36608538 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-1543G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608538 | |||||||
chr11:36608592 | A | G | 27 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-23-1489A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608592 | |||||||
chr11:36608624 | CT | C | 5 | a0001c0001t0001g0141 a0001c0001t0002g0229 a0002c0003t0002g0014 others(2): Show |
6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1456delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608624 | |||||||
chr11:36608704 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-23-1377T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608704 | |||||||
chr11:36608729 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-23-1352A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608729 | |||||||
chr11:36608817 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23-1264T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608817 | |||||||
chr11:36608825 | A | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-1256A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608825 | |||||||
chr11:36608868 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-23-1213T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608868 | |||||||
chr11:36608927 | TG | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-1153delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608927 | |||||||
chr11:36608992 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-23-1089T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608992 | |||||||
chr11:36609204 | C | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-877C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609204 | |||||||
chr11:36609231 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-23-850G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609231 | |||||||
chr11:36609335 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-23-746C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609335 | |||||||
chr11:36609442 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-23-639G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609442 | |||||||
chr11:36609489 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-23-592A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609489 | |||||||
chr11:36609873 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0239 a0001c0001t0001g0255 |
4 | NA18951.hp2 NA18978.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-208G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609873 | |||||||
chr11:36610317 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+78G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610317 | |||||||
chr11:36610327 | A | G | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+88A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610327 | |||||||
chr11:36610635 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+396C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610635 | |||||||
chr11:36610724 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.136+485G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610724 | |||||||
chr11:36610816 | ATGC | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+598_136+600del others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36610816 | ||||||
chr11:36610833 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(62): Show |
93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.136+594G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610833 | |||||||
chr11:36610850 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+611T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610850 | |||||||
chr11:36610965 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(164): Show |
233 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.136+726G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610965 | |||||||
chr11:36610989 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+750C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610989 | |||||||
chr11:36611006 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.136+767G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611006 | |||||||
chr11:36611034 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136+795A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611034 | |||||||
chr11:36611085 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.136+846A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611085 | |||||||
chr11:36611228 | A | G | 21 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(18): Show |
26 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.136+989A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611228 | |||||||
chr11:36611236 | C | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+997C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611236 | |||||||
chr11:36611255 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+1016G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611255 | |||||||
chr11:36611392 | T | TA | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1160dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36611392 | ||||||
chr11:36611558 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136+1319T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611558 | |||||||
chr11:36611581 | G | A | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1342G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611581 | |||||||
chr11:36611613 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136+1374T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611613 | |||||||
chr11:36611752 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0038 others(84): Show |
120 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.136+1513A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611752 | |||||||
chr11:36611852 | A | C | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.136+1613A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611852 | |||||||
chr11:36612017 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+1778C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612017 | |||||||
chr11:36612056 | A | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1817A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612056 | |||||||
chr11:36612066 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136+1827C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612066 | |||||||
chr11:36612280 | G | GT | 40 | a0001c0001t0001g0168 a0001c0001t0002g0016 a0001c0001t0002g0024 others(37): Show |
46 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+2052dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36612280 | ||||||
chr11:36612528 | A | G | 5 | a0001c0001t0002g0032 a0001c0001t0002g0211 a0001c0001t0002g0212 others(2): Show |
6 | HG01496.hp1 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+2289A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612528 | |||||||
chr11:36612547 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+2308A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612547 | |||||||
chr11:36612561 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136+2322C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612561 | |||||||
chr11:36612669 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0002g0201 a0001c0001t0002g0202 |
4 | HG02572.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+2430G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612669 | |||||||
chr11:36612718 | T | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+2479T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612718 | |||||||
chr11:36612842 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2603A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612842 | |||||||
chr11:36612995 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.136+2756G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612995 | |||||||
chr11:36613069 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.136+2830C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613069 | |||||||
chr11:36613070 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.136+2831G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613070 | |||||||
chr11:36613099 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2860C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613099 | |||||||
chr11:36613184 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2945T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613184 | |||||||
chr11:36613203 | T | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+2964T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613203 | |||||||
chr11:36613229 | A | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+2990A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613229 | |||||||
chr11:36613239 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+3000G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613239 | |||||||
chr11:36613280 | C | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+3041C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613280 | |||||||
chr11:36613588 | A | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+3349A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613588 | |||||||
chr11:36613599 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+3360C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613599 | |||||||
chr11:36613619 | C | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+3380C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613619 | |||||||
chr11:36613667 | A | G | 1 | a0001c0002t0003g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136+3428A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613667 | |||||||
chr11:36613853 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3614C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613853 | |||||||
chr11:36613879 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.136+3640G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613879 | |||||||
chr11:36613890 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0214 |
3 | HG03139.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136+3651C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613890 | |||||||
chr11:36613894 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.136+3655T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613894 | |||||||
chr11:36613898 | TTTG | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(61): Show |
92 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.136+3669_136+3671d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36613898 | ||||||
chr11:36613905 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.136+3666T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613905 | |||||||
chr11:36613916 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.136+3677T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613916 | |||||||
chr11:36613917 | CT | C | 41 | a0001c0001t0001g0073 a0001c0001t0001g0104 a0001c0001t0002g0016 others(38): Show |
47 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.136+3690delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36613917 | ||||||
chr11:36613984 | G | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+3745G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613984 | |||||||
chr11:36614103 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3864A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614103 | |||||||
chr11:36614119 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.136+3880C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614119 | |||||||
chr11:36614126 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3887A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614126 | |||||||
chr11:36614153 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(165): Show |
234 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.136+3914T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614153 | |||||||
chr11:36614160 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3921T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614160 | |||||||
chr11:36614182 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3943T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614182 | |||||||
chr11:36614236 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+3997A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614236 | |||||||
chr11:36614239 | G | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+4000G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614239 | |||||||
chr11:36614242 | A | G | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+4003A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614242 | |||||||
chr11:36614344 | C | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4105C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614344 | |||||||
chr11:36614353 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+4114A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614353 | |||||||
chr11:36614362 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.136+4123A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614362 | |||||||
chr11:36614415 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.136+4176G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614415 | |||||||
chr11:36614418 | C | A | 1 | a0001c0001t0002g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.136+4179C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614418 | |||||||
chr11:36614572 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4333C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614572 | |||||||
chr11:36614576 | G | A | 2 | a0001c0001t0002g0215 a0001c0001t0002g0227 |
2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.136+4337G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614576 | |||||||
chr11:36614651 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+4412A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614651 | |||||||
chr11:36614675 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4436G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614675 | |||||||
chr11:36614675 | G | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+4436G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614675 | |||||||
chr11:36614777 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0166 |
2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.136+4538C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614777 | |||||||
chr11:36614809 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4570C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614809 | |||||||
chr11:36614810 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4571T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614810 | |||||||
chr11:36614830 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4591G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614830 | |||||||
chr11:36614833 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4594G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614833 | |||||||
chr11:36614835 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4596G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614835 | |||||||
chr11:36614839 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4600A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614839 | |||||||
chr11:36614840 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4601T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614840 | |||||||
chr11:36614851 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4612T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614851 | |||||||
chr11:36614872 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4633C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614872 | |||||||
chr11:36614874 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4635G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614874 | |||||||
chr11:36614875 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4636T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614875 | |||||||
chr11:36614886 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4647G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614886 | |||||||
chr11:36614887 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4648G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614887 | |||||||
chr11:36614898 | A | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+4659A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614898 | |||||||
chr11:36614900 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4661C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614900 | |||||||
chr11:36614912 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4673T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614912 | |||||||
chr11:36614925 | T | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+4686T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614925 | |||||||
chr11:36614950 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4711T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614950 | |||||||
chr11:36614962 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4723G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614962 | |||||||
chr11:36614966 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4727T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614966 | |||||||
chr11:36614967 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4728T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614967 | |||||||
chr11:36614969 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4730G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614969 | |||||||
chr11:36614970 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4731T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614970 | |||||||
chr11:36614971 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4732G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614971 | |||||||
chr11:36614972 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4733T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614972 | |||||||
chr11:36614975 | C | T | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+4736C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614975 | |||||||
chr11:36614976 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4737A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614976 | |||||||
chr11:36614976 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+4737A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614976 | |||||||
chr11:36614977 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4738G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614977 | |||||||
chr11:36614984 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4745A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614984 | |||||||
chr11:36614985 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4746G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614985 | |||||||
chr11:36614989 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4750T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614989 | |||||||
chr11:36614992 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4753C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614992 | |||||||
chr11:36615066 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.136+4827G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615066 | |||||||
chr11:36615137 | T | G | 1 | a0001c0001t0002g0216 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.136+4898T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615137 | |||||||
chr11:36615238 | A | G | 53 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
63 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.136+4999A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615238 | |||||||
chr11:36615240 | C | T | 29 | a0001c0001t0001g0025 a0001c0001t0002g0024 a0001c0001t0002g0032 others(26): Show |
36 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.136+5001C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615240 | |||||||
chr11:36615351 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.136+5112T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615351 | |||||||
chr11:36615389 | C | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+5150C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615389 | |||||||
chr11:36615395 | C | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+5156C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615395 | |||||||
chr11:36615424 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136+5185A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615424 | |||||||
chr11:36615579 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+5340A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615579 | |||||||
chr11:36615581 | G | C | 40 | a0001c0001t0001g0166 a0001c0001t0002g0016 a0001c0001t0002g0024 others(37): Show |
46 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+5342G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615581 | |||||||
chr11:36615765 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+5526T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615765 | |||||||
chr11:36615767 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.136+5528G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615767 | |||||||
chr11:36615854 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.136+5615G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615854 | |||||||
chr11:36615883 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(130): Show |
175 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.136+5644T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615883 | |||||||
chr11:36616006 | G | A | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+5767G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616006 | |||||||
chr11:36616007 | T | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01981.hp1 HG02080.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+5768T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616007 | |||||||
chr11:36616016 | C | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01981.hp1 HG02080.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+5777C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616016 | |||||||
chr11:36616024 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.136+5785G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616024 | |||||||
chr11:36616057 | A | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0206 others(1): Show |
6 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+5818A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616057 | |||||||
chr11:36616138 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0166 |
2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.136+5899C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616138 | |||||||
chr11:36616497 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+6258A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616497 | |||||||
chr11:36616563 | C | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0038 others(33): Show |
60 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.136+6324C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616563 | |||||||
chr11:36616617 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+6378A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616617 | |||||||
chr11:36616627 | C | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
9 | HG00544.hp1 HG01934.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+6388C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616627 | |||||||
chr11:36616645 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6406A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616645 | |||||||
chr11:36616677 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136+6438G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616677 | |||||||
chr11:36616784 | G | A | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+6545G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616784 | |||||||
chr11:36616785 | T | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+6546T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616785 | |||||||
chr11:36616813 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.136+6574G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616813 | |||||||
chr11:36616817 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+6578T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616817 | |||||||
chr11:36616871 | TA | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6639delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36616871 | ||||||
chr11:36616887 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+6648C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616887 | |||||||
chr11:36616949 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6710C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616949 | |||||||
chr11:36617047 | A | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+6808A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617047 | |||||||
chr11:36617138 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+6899T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617138 | |||||||
chr11:36617158 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6919C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617158 | |||||||
chr11:36617160 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.136+6921T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617160 | |||||||
chr11:36617165 | AATG | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0220 |
3 | HG00733.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.136+6929_136+6931d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36617165 | ||||||
chr11:36617198 | T | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+6959T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617198 | |||||||
chr11:36617351 | C | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+7112C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617351 | |||||||
chr11:36617360 | TG | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0040 others(24): Show |
46 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+7123delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36617360 | ||||||
chr11:36617382 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7143A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617382 | |||||||
chr11:36617477 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+7238G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617477 | |||||||
chr11:36617512 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.136+7273G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617512 | |||||||
chr11:36617530 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.136+7291T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617530 | |||||||
chr11:36617549 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0242 others(4): Show |
10 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+7310T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617549 | |||||||
chr11:36617650 | T | C | 1 | a0003c0006t0001g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136+7411T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617650 | |||||||
chr11:36617709 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7470G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617709 | |||||||
chr11:36617725 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.136+7486G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617725 | |||||||
chr11:36617814 | T | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7575T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617814 | |||||||
chr11:36617891 | G | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7652G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617891 | |||||||
chr11:36618041 | G | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+7802G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618041 | |||||||
chr11:36618134 | G | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(62): Show |
93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.136+7895G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618134 | |||||||
chr11:36618174 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.136+7935A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618174 | |||||||
chr11:36618237 | G | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+7998G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618237 | |||||||
chr11:36618246 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8007C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618246 | |||||||
chr11:36618630 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+8391G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618630 | |||||||
chr11:36618696 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8457G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618696 | |||||||
chr11:36618716 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+8477C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618716 | |||||||
chr11:36618923 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8684G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618923 | |||||||
chr11:36618931 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.136+8692A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618931 | |||||||
chr11:36618994 | C | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+8755C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618994 | |||||||
chr11:36619044 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0239 a0001c0001t0001g0255 |
4 | NA18951.hp2 NA18978.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+8805C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619044 | |||||||
chr11:36619234 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.136+8995A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619234 | |||||||
chr11:36619267 | G | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9028G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619267 | |||||||
chr11:36619307 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136+9068C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619307 | |||||||
chr11:36619313 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.136+9074C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619313 | |||||||
chr11:36619314 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.136+9075G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619314 | |||||||
chr11:36619325 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.136+9086A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619325 | |||||||
chr11:36619427 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.136+9188A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619427 | |||||||
chr11:36619432 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9193A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619432 | |||||||
chr11:36619455 | G | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+9216G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619455 | |||||||
chr11:36619558 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136+9319A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619558 | |||||||
chr11:36619899 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+9660A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619899 | |||||||
chr11:36619955 | A | AGACATAG others(7): Show |
166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(163): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.136+9718_136+9731d others(16): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36619955 | ||||||
chr11:36620034 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+9795C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620034 | |||||||
chr11:36620204 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.136+9965A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620204 | |||||||
chr11:36620217 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9978A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620217 | |||||||
chr11:36620256 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.136+10017G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620256 | |||||||
chr11:36620273 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+10034A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620273 | |||||||
chr11:36620280 | C | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10041C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620280 | |||||||
chr11:36620283 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.136+10044A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620283 | |||||||
chr11:36620427 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+10188G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620427 | |||||||
chr11:36620639 | G | T | 41 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0016 others(38): Show |
47 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.136+10400G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620639 | |||||||
chr11:36620652 | A | G | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(13): Show |
19 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.136+10413A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620652 | |||||||
chr11:36620740 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+10501C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620740 | |||||||
chr11:36620812 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136+10573T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620812 | |||||||
chr11:36620823 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(126): Show |
171 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.136+10584C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620823 | |||||||
chr11:36620864 | ATTGT | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10629_136+1063 others(8): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36620864 | ||||||
chr11:36620935 | ATAAAT | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10699_136+1070 others(9): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36620935 | ||||||
chr11:36620954 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.136+10715T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620954 | |||||||
chr11:36620969 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10730G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620969 | |||||||
chr11:36621009 | G | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10770G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621009 | |||||||
chr11:36621010 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10771T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621010 | |||||||
chr11:36621013 | A | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+10774A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621013 | |||||||
chr11:36621014 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10775A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621014 | |||||||
chr11:36621140 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10901G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621140 | |||||||
chr11:36621251 | TTAGCAA | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+11013_136+1101 others(10): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621251 | |||||||
chr11:36621380 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.136+11141C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621380 | |||||||
chr11:36621660 | T | G | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+11421T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621660 | |||||||
chr11:36621695 | C | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.136+11456C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621695 | |||||||
chr11:36621724 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.136+11485G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621724 | |||||||
chr11:36622061 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-11223T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622061 | |||||||
chr11:36622069 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0252 |
2 | NA18964.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.137-11215T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622069 | |||||||
chr11:36622083 | A | ATTTTTTT | 26 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-11195_137-1119 others(11): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622083 | ||||||
chr11:36622083 | A | ATTTTTTT others(1): Show |
7 | a0001c0001t0002g0049 a0001c0001t0002g0057 a0001c0001t0002g0207 others(4): Show |
7 | HG01517.hp2 HG02523.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-11195_137-1119 others(12): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622083 | ||||||
chr11:36622088 | TTA | T | 8 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0181 others(5): Show |
8 | HG01074.hp2 HG01192.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-11194_137-1119 others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622088 | ||||||
chr11:36622089 | TA | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(54): Show |
85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.137-11194delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622089 | |||||||
chr11:36622090 | A | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0031 others(56): Show |
71 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.137-11194A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622090 | |||||||
chr11:36622168 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137-11116C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622168 | |||||||
chr11:36622401 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10883G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622401 | |||||||
chr11:36622483 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-10801C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622483 | |||||||
chr11:36622526 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10758A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622526 | |||||||
chr11:36622549 | C | G | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-10735C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622549 | |||||||
chr11:36622596 | C | G | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-10688C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622596 | |||||||
chr11:36622707 | CAT | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0099 |
3 | HG02523.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-10576_137-1057 others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622707 | |||||||
chr11:36622712 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-10572G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622712 | |||||||
chr11:36622719 | T | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-10565T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622719 | |||||||
chr11:36622748 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10536C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622748 | |||||||
chr11:36622800 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0236 |
5 | HG01243.hp1 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-10484T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622800 | |||||||
chr11:36623004 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.137-10280A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623004 | |||||||
chr11:36623031 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10253T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623031 | |||||||
chr11:36623100 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-10184T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623100 | |||||||
chr11:36623128 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137-10156G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623128 | |||||||
chr11:36623143 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10141T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623143 | |||||||
chr11:36623172 | C | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-10112C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623172 | |||||||
chr11:36623317 | T | TC | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9967_137-9966i others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623317 | |||||||
chr11:36623353 | T | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9931T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623353 | |||||||
chr11:36623356 | T | TC | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(69): Show |
103 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.137-9919dupC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623356 | ||||||
chr11:36623490 | C | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-9794C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623490 | |||||||
chr11:36623657 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9627C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623657 | |||||||
chr11:36623681 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9603C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623681 | |||||||
chr11:36623707 | A | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9577A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623707 | |||||||
chr11:36623745 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137-9539A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623745 | |||||||
chr11:36623826 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9458G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623826 | |||||||
chr11:36623853 | AG | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9430delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623853 | |||||||
chr11:36623860 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-9424C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623860 | |||||||
chr11:36623861 | G | A | 47 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0111 others(44): Show |
55 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.137-9423G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623861 | |||||||
chr11:36623863 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.137-9421A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623863 | |||||||
chr11:36623967 | TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.137-9293_137-9280d others(16): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623967 | ||||||
chr11:36623995 | G | GTA | 14 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(11): Show |
15 | HG01516.hp2 HG01517.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-9279_137-9278d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623995 | ||||||
chr11:36624005 | A | ATT | 23 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(20): Show |
28 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.137-9273_137-9272d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36624005 | ||||||
chr11:36624005 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0058 others(8): Show |
16 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-9279A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624005 | |||||||
chr11:36624043 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.137-9241C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624043 | |||||||
chr11:36624079 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-9205C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624079 | |||||||
chr11:36624176 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.137-9108A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624176 | |||||||
chr11:36624335 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.137-8949G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624335 | |||||||
chr11:36624337 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8947G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624337 | |||||||
chr11:36624389 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-8895G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624389 | |||||||
chr11:36624490 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8794C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624490 | |||||||
chr11:36624514 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8770C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624514 | |||||||
chr11:36624576 | C | G | 27 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.137-8708C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624576 | |||||||
chr11:36624680 | C | T | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-8604C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624680 | |||||||
chr11:36624692 | G | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-8592G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624692 | |||||||
chr11:36624727 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-8557G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624727 | |||||||
chr11:36624766 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-8518T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624766 | |||||||
chr11:36624772 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-8512G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624772 | |||||||
chr11:36624800 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-8484C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624800 | |||||||
chr11:36624808 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.137-8476T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624808 | |||||||
chr11:36624840 | A | AAAC | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8444_137-8443i others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624840 | |||||||
chr11:36624841 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8443G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624841 | |||||||
chr11:36624842 | G | A | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8442G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624842 | |||||||
chr11:36625013 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-8271A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625013 | |||||||
chr11:36625040 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-8244A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625040 | |||||||
chr11:36625178 | T | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-8106T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625178 | |||||||
chr11:36625289 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.137-7995A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625289 | |||||||
chr11:36625295 | T | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-7989T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625295 | |||||||
chr11:36625319 | A | C | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-7965A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625319 | |||||||
chr11:36625460 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-7824A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625460 | |||||||
chr11:36625611 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-7673G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625611 | |||||||
chr11:36625756 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0082 |
3 | HG00099.hp2 HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.137-7528G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625756 | |||||||
chr11:36625794 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-7490G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625794 | |||||||
chr11:36625905 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.137-7379C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625905 | |||||||
chr11:36625907 | AGTGCAAA others(7347): Show |
A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0197 others(3): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-7376_137-23del | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625907 | |||||||
chr11:36626241 | T | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-7043T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626241 | |||||||
chr11:36626482 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-6802G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626482 | |||||||
chr11:36626528 | C | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-6756C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626528 | |||||||
chr11:36626570 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0231 |
3 | HG02451.hp1 NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-6714C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626570 | |||||||
chr11:36626635 | C | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-6649C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626635 | |||||||
chr11:36626722 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137-6562C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626722 | |||||||
chr11:36626882 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-6402G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626882 | |||||||
chr11:36626896 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-6388C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626896 | |||||||
chr11:36627091 | C | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-6193C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627091 | |||||||
chr11:36627343 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137-5941C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627343 | |||||||
chr11:36627345 | C | A | 1 | a0001c0001t0001g0048 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.137-5939C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627345 | |||||||
chr11:36627425 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-5859T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627425 | |||||||
chr11:36627631 | G | T | 1 | a0001c0001t0001g0001 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-5653G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627631 | |||||||
chr11:36627648 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-5636C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627648 | |||||||
chr11:36627813 | A | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5471A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627813 | |||||||
chr11:36628001 | T | C | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.137-5283T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628001 | |||||||
chr11:36628004 | G | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01099.hp2 HG01106.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5280G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628004 | |||||||
chr11:36628009 | C | CT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0135 others(7): Show |
11 | HG01109.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-5262dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | ||||||
chr11:36628009 | C | CTT | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-5263_137-5262d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | ||||||
chr11:36628009 | CT | C | 27 | a0001c0001t0001g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
32 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.137-5262delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | ||||||
chr11:36628054 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-5230T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628054 | |||||||
chr11:36628172 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-5112T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628172 | |||||||
chr11:36628425 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-4859G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628425 | |||||||
chr11:36628616 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137-4668T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628616 | |||||||
chr11:36628634 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-4650C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628634 | |||||||
chr11:36628703 | T | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-4581T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628703 | |||||||
chr11:36628807 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-4477A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628807 | |||||||
chr11:36628998 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-4286G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628998 | |||||||
chr11:36629244 | A | C | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.137-4040A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629244 | |||||||
chr11:36629287 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.137-3997T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629287 | |||||||
chr11:36629366 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-3918A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629366 | |||||||
chr11:36629743 | G | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-3541G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629743 | |||||||
chr11:36629910 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.137-3374C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629910 | |||||||
chr11:36629957 | T | G | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-3327T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629957 | |||||||
chr11:36630001 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.137-3283A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630001 | |||||||
chr11:36630354 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-2930G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630354 | |||||||
chr11:36630590 | A | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-2694A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630590 | |||||||
chr11:36630655 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-2629T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630655 | |||||||
chr11:36630669 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0104 a0001c0001t0001g0107 others(1): Show |
4 | HG00621.hp1 HG02155.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-2615C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630669 | |||||||
chr11:36630765 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2519A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630765 | |||||||
chr11:36630886 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.137-2398G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630886 | |||||||
chr11:36630956 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.137-2328A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630956 | |||||||
chr11:36630989 | C | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2295C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630989 | |||||||
chr11:36631019 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-2265C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631019 | |||||||
chr11:36631247 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-2037T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631247 | |||||||
chr11:36631267 | TGGTG | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-2016_137-2013d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631267 | |||||||
chr11:36631336 | G | A | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1948G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631336 | |||||||
chr11:36631434 | G | A | 13 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.137-1850G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631434 | |||||||
chr11:36631645 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.137-1639A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631645 | |||||||
chr11:36631723 | T | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1561T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631723 | |||||||
chr11:36631726 | A | G | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1558A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631726 | |||||||
chr11:36631766 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-1518C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631766 | |||||||
chr11:36631793 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-1491C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631793 | |||||||
chr11:36631799 | T | C | 37 | a0001c0001t0002g0016 a0001c0001t0002g0032 a0001c0001t0002g0033 others(34): Show |
42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.137-1485T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631799 | |||||||
chr11:36631913 | ATTC | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0231 |
3 | HG02451.hp1 NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-1365_137-1363d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36631913 | ||||||
chr11:36632028 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-1256G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632028 | |||||||
chr11:36632179 | T | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0156 others(1): Show |
5 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-1105T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632179 | |||||||
chr11:36632181 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.137-1103T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632181 | |||||||
chr11:36632299 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.137-985G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632299 | |||||||
chr11:36632412 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.137-872C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632412 | |||||||
chr11:36632609 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-675A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632609 | |||||||
chr11:36632786 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-498C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632786 | |||||||
chr11:36632920 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-364G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632920 | |||||||
chr11:36632953 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.137-331A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632953 | |||||||
chr11:36633072 | T | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-212T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633072 | |||||||
chr11:36633086 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-198G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633086 | |||||||
chr11:36633162 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.137-122C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633162 | |||||||
chr11:36633164 | G | A | 2 | a0001c0001t0002g0215 a0001c0001t0002g0227 |
2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.137-120G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633164 | |||||||
chr11:36633263 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0197 others(3): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-21G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633263 | |||||||
chr11:36633265 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0197 others(3): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-19G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633265 | |||||||
chr11:36633266 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0197 others(3): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-18C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633266 | |||||||
chr11:36633270 | AC | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0197 others(3): Show |
10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-13delC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633270 | |||||||
chr11:36633499 | C | CA | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+69dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36633499 | ||||||
chr11:36633539 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.291+101A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633539 | |||||||
chr11:36633738 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+300A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633738 | |||||||
chr11:36633816 | G | A | 1 | a0001c0002t0003g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.291+378G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633816 | |||||||
chr11:36633825 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.291+387G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633825 | |||||||
chr11:36633849 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+411C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633849 | |||||||
chr11:36634026 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+588A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634026 | |||||||
chr11:36634201 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
109 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.291+763T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634201 | |||||||
chr11:36634234 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
236 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.291+796G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634234 | |||||||
chr11:36634256 | A | G | 1 | a0003c0006t0001g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.291+818A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634256 | |||||||
chr11:36634314 | G | T | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.291+876G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634314 | |||||||
chr11:36634336 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+898T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634336 | |||||||
chr11:36634339 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(130): Show |
175 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.291+901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634339 | |||||||
chr11:36634383 | C | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.291+945C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634383 | |||||||
chr11:36634461 | G | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(13): Show |
19 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.291+1023G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634461 | |||||||
chr11:36634544 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.291+1106A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634544 | |||||||
chr11:36634814 | AT | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-1228delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36634814 | ||||||
chr11:36634889 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.292-1162G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634889 | |||||||
chr11:36634946 | G | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1105G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634946 | |||||||
chr11:36634949 | TACACCAC others(23): Show |
T | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
4 | HG02257.hp1 HG02280.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1098_292-1069d others(32): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36634949 | ||||||
chr11:36634990 | A | T | 1 | a0001c0001t0002g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292-1061A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634990 | |||||||
chr11:36635063 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-988G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635063 | |||||||
chr11:36635066 | T | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-985T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635066 | |||||||
chr11:36635067 | G | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-984G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635067 | |||||||
chr11:36635068 | T | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-983T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635068 | |||||||
chr11:36635106 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-945G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635106 | |||||||
chr11:36635207 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-844A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635207 | |||||||
chr11:36635257 | C | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292-794C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635257 | |||||||
chr11:36635304 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-747A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635304 | |||||||
chr11:36635395 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0124 |
2 | HG01123.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.292-656G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635395 | |||||||
chr11:36635409 | A | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-642A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635409 | |||||||
chr11:36635440 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-611A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635440 | |||||||
chr11:36635505 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292-546C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635505 | |||||||
chr11:36635668 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.292-383G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635668 | |||||||
chr11:36635692 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(162): Show |
231 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.292-359G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635692 | |||||||
chr11:36635722 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-329A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635722 | |||||||
chr11:36635808 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-243A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635808 | |||||||
chr11:36635827 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.292-224G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635827 | |||||||
chr11:36635863 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292-188T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635863 | |||||||
chr11:36635987 | CTT | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-61_292-60delTT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36635987 | ||||||
chr11:36636225 | A | G | 28 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(25): Show |
34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.358+108A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636225 | |||||||
chr11:36636361 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.358+244T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636361 | |||||||
chr11:36636598 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+481G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636598 | |||||||
chr11:36636604 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+487C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636604 | |||||||
chr11:36636732 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+615T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636732 | |||||||
chr11:36636770 | A | AT | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+657dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636770 | ||||||
chr11:36636836 | C | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+719C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636836 | |||||||
chr11:36636889 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+772C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636889 | |||||||
chr11:36636922 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+805A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636922 | |||||||
chr11:36636923 | GT | G | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0105 others(10): Show |
13 | HG00099.hp2 HG01074.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+824delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | ||||||
chr11:36636923 | GTT | G | 46 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(43): Show |
53 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.358+823_358+824del others(2): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | ||||||
chr11:36636923 | GTTT | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+822_358+824del others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | ||||||
chr11:36636930 | T | G | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+813T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636930 | |||||||
chr11:36636946 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.358+829A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636946 | |||||||
chr11:36637023 | T | C | 27 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.358+906T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637023 | |||||||
chr11:36637064 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+947G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637064 | |||||||
chr11:36637272 | A | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+1155A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637272 | |||||||
chr11:36637273 | G | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1156G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637273 | |||||||
chr11:36637324 | C | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1207C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637324 | |||||||
chr11:36637549 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.358+1432G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637549 | |||||||
chr11:36637651 | C | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1534C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637651 | |||||||
chr11:36637651 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.358+1534C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637651 | |||||||
chr11:36637661 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1544A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637661 | |||||||
chr11:36637885 | C | CTT | 38 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(35): Show |
44 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.358+1780_358+1781d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | ||||||
chr11:36637885 | C | CTTT | 14 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(11): Show |
17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.358+1779_358+1781d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | ||||||
chr11:36637885 | CT | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0038 others(34): Show |
61 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1781delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | ||||||
chr11:36637902 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(10): Show |
16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+1785A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637902 | |||||||
chr11:36638037 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
174 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.358+1920T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638037 | |||||||
chr11:36638134 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.358+2017G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638134 | |||||||
chr11:36638153 | G | C | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2036G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638153 | |||||||
chr11:36638156 | C | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+2039C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638156 | |||||||
chr11:36638221 | T | G | 1 | a0001c0001t0001g0038 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.358+2104T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638221 | |||||||
chr11:36638344 | A | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+2227A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638344 | |||||||
chr11:36638415 | C | A | 26 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(23): Show |
30 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(27): Show |
intron_variant | MODIFIER | c.358+2298C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638415 | |||||||
chr11:36638446 | G | T | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2329G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638446 | |||||||
chr11:36638468 | A | G | 52 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(49): Show |
61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2351A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638468 | |||||||
chr11:36638584 | G | A | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2467G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638584 | |||||||
chr11:36638819 | C | G | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358+2702C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638819 | |||||||
chr11:36638941 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0209 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.358+2824T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638941 | |||||||
chr11:36639018 | A | G | 4 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0206 others(1): Show |
6 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+2901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639018 | |||||||
chr11:36639082 | C | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+2965C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639082 | |||||||
chr11:36639156 | TTAGAA | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+3043_358+3047d others(7): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639156 | ||||||
chr11:36639169 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0166 |
2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.358+3052A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639169 | |||||||
chr11:36639253 | C | CT | 50 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(47): Show |
58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.358+3150dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639253 | ||||||
chr11:36639409 | GTTCTCCA others(9): Show |
G | 1 | a0001c0001t0001g0029 | 2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.358+3297_358+3312d others(18): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639409 | ||||||
chr11:36639454 | A | G | 1 | a0001c0001t0001g0043 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.358+3337A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639454 | |||||||
chr11:36639500 | A | G | 38 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(35): Show |
46 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.358+3383A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639500 | |||||||
chr11:36639537 | G | A | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+3420G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639537 | |||||||
chr11:36639569 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.358+3452A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639569 | |||||||
chr11:36639600 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.358+3483C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639600 | |||||||
chr11:36639674 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
6 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+3557G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639674 | |||||||
chr11:36639711 | G | A | 40 | a0001c0001t0001g0008 a0001c0001t0001g0135 a0001c0001t0001g0136 others(37): Show |
51 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.358+3594G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639711 | |||||||
chr11:36639731 | G | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+3614G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639731 | |||||||
chr11:36639775 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.358+3658C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639775 | |||||||
chr11:36639852 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
169 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.358+3735G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639852 | |||||||
chr11:36639893 | C | T | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+3776C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639893 | |||||||
chr11:36639897 | T | C | 1 | a0001c0002t0003g0203 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+3780T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639897 | |||||||
chr11:36639956 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.358+3839C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639956 | |||||||
chr11:36640046 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.358+3929A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640046 | |||||||
chr11:36640117 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.358+4000A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640117 | |||||||
chr11:36640173 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4056A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640173 | |||||||
chr11:36640286 | TTG | T | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4173_358+4174d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36640286 | ||||||
chr11:36640338 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358+4221C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640338 | |||||||
chr11:36640383 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.358+4266T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640383 | |||||||
chr11:36640399 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+4282T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640399 | |||||||
chr11:36640450 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358+4333A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640450 | |||||||
chr11:36640667 | G | A | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4550G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640667 | |||||||
chr11:36640966 | G | T | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4849G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640966 | |||||||
chr11:36641014 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+4897C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641014 | |||||||
chr11:36641053 | A | G | 5 | a0001c0001t0001g0141 a0001c0001t0002g0229 a0002c0003t0002g0014 others(2): Show |
6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+4936A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641053 | |||||||
chr11:36641660 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358+5543C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641660 | |||||||
chr11:36641756 | T | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.358+5639T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641756 | |||||||
chr11:36641790 | C | A | 1 | a0001c0001t0001g0045 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.358+5673C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641790 | |||||||
chr11:36642052 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.358+5935C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642052 | |||||||
chr11:36642053 | T | G | 1 | a0001c0001t0002g0053 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.358+5936T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642053 | |||||||
chr11:36642089 | A | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00099.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.359-5927A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642089 | |||||||
chr11:36642103 | C | A | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-5913C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642103 | |||||||
chr11:36642103 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-5913C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642103 | |||||||
chr11:36642104 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.359-5912C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642104 | |||||||
chr11:36642172 | G | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-5844G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642172 | |||||||
chr11:36642235 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.359-5781A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642235 | |||||||
chr11:36642255 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.359-5761A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642255 | |||||||
chr11:36642281 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
109 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.359-5735C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642281 | |||||||
chr11:36642282 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5734A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642282 | |||||||
chr11:36642414 | A | C | 5 | a0001c0001t0001g0141 a0001c0001t0002g0229 a0002c0003t0002g0014 others(2): Show |
6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-5602A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642414 | |||||||
chr11:36642429 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.359-5587C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642429 | |||||||
chr11:36642470 | G | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5546G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642470 | |||||||
chr11:36642591 | C | T | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-5425C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642591 | |||||||
chr11:36642715 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5301A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642715 | |||||||
chr11:36642742 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.359-5274A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642742 | |||||||
chr11:36643070 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.359-4946C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643070 | |||||||
chr11:36643095 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-4921A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643095 | |||||||
chr11:36643152 | G | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0078 others(14): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.359-4864G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643152 | |||||||
chr11:36643159 | G | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359-4857G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643159 | |||||||
chr11:36643162 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-4854A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643162 | |||||||
chr11:36643180 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0161 a0001c0001t0001g0192 others(1): Show |
6 | HG00438.hp2 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-4836A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643180 | |||||||
chr11:36643338 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.359-4678G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643338 | |||||||
chr11:36643357 | A | G | 1 | a0001c0002t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.359-4659A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643357 | |||||||
chr11:36643379 | C | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4637C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643379 | |||||||
chr11:36643383 | A | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4633A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643383 | |||||||
chr11:36643469 | A | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-4547A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643469 | |||||||
chr11:36643469 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-4547A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643469 | |||||||
chr11:36643493 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.359-4523A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643493 | |||||||
chr11:36643545 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.359-4471T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643545 | |||||||
chr11:36643600 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0111 |
3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.359-4416G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643600 | |||||||
chr11:36643605 | A | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4411A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643605 | |||||||
chr11:36643636 | G | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-4380G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643636 | |||||||
chr11:36643802 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.359-4214A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643802 | |||||||
chr11:36643893 | C | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0221 |
3 | HG00738.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.359-4123C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643893 | |||||||
chr11:36644002 | T | A | 1 | a0001c0001t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.359-4014T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644002 | |||||||
chr11:36644021 | G | T | 34 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0032 others(31): Show |
41 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.359-3995G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644021 | |||||||
chr11:36644041 | T | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-3975T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644041 | |||||||
chr11:36644045 | A | C | 45 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(42): Show |
51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.359-3971A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644045 | |||||||
chr11:36644099 | A | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
275 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.359-3917A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644099 | |||||||
chr11:36644103 | A | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0149 a0001c0001t0001g0160 |
4 | HG00735.hp2 NA18966.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-3913A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644103 | |||||||
chr11:36644233 | C | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3783C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644233 | |||||||
chr11:36644234 | G | A | 13 | a0001c0001t0001g0103 a0001c0001t0001g0129 a0001c0001t0002g0016 others(10): Show |
13 | HG00438.hp1 HG01358.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.359-3782G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644234 | |||||||
chr11:36644235 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3781G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644235 | |||||||
chr11:36644236 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3780G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644236 | |||||||
chr11:36644237 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359-3779C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644237 | |||||||
chr11:36644394 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.359-3622G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644394 | |||||||
chr11:36644405 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0147 a0001c0001t0001g0149 others(1): Show |
5 | HG00735.hp2 HG03654.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-3611T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644405 | |||||||
chr11:36644564 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.359-3452G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644564 | |||||||
chr11:36644766 | T | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-3250T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644766 | |||||||
chr11:36644767 | G | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-3249G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644767 | |||||||
chr11:36644768 | A | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-3248A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644768 | |||||||
chr11:36644782 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-3234T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644782 | |||||||
chr11:36644855 | T | TG | 54 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(51): Show |
66 | HG00408.hp2 HG00544.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.359-3155dupG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644855 | ||||||
chr11:36644862 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.359-3154A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644862 | |||||||
chr11:36644880 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-3136A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644880 | |||||||
chr11:36644905 | A | G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3111A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644905 | |||||||
chr11:36644906 | G | A | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3110G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644906 | |||||||
chr11:36644993 | T | TATA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0128 others(7): Show |
14 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-3000_359-2998d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644993 | ||||||
chr11:36644993 | TATA | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0038 others(74): Show |
109 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-3000_359-2998d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644993 | ||||||
chr11:36645054 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-2962A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645054 | |||||||
chr11:36645160 | A | C | 2 | a0001c0001t0002g0210 a0001c0001t0002g0217 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.359-2856A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645160 | |||||||
chr11:36645381 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.359-2635A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645381 | |||||||
chr11:36645391 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-2625G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645391 | |||||||
chr11:36645396 | C | T | 1 | a0001c0001t0004g0235 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-2620C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645396 | |||||||
chr11:36645456 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.359-2560G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645456 | |||||||
chr11:36645485 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-2531T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645485 | |||||||
chr11:36645544 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.359-2472T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645544 | |||||||
chr11:36645649 | T | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2367T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645649 | |||||||
chr11:36645689 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-2327T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645689 | |||||||
chr11:36645949 | A | T | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2067A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645949 | |||||||
chr11:36646000 | T | C | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-2016T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646000 | |||||||
chr11:36646031 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(61): Show |
92 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.359-1985C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646031 | |||||||
chr11:36646044 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-1972G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646044 | |||||||
chr11:36646088 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.359-1928A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646088 | |||||||
chr11:36646340 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.359-1676T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646340 | |||||||
chr11:36646436 | G | T | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-1580G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646436 | |||||||
chr11:36646628 | AT | A | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-1385delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36646628 | ||||||
chr11:36646708 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.359-1308T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646708 | |||||||
chr11:36646848 | T | C | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-1168T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646848 | |||||||
chr11:36647171 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG02258.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-845G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647171 | |||||||
chr11:36647462 | T | C | 53 | a0001c0001t0001g0037 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
63 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.359-554T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647462 | |||||||
chr11:36647468 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.359-548T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647468 | |||||||
chr11:36647580 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
166 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.359-436C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647580 | |||||||
chr11:36647660 | A | G | 27 | a0001c0001t0001g0037 a0001c0001t0002g0032 a0001c0001t0002g0033 others(24): Show |
33 | HG00673.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-356A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647660 | |||||||
chr11:36647691 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.359-325A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647691 | |||||||
chr11:36647804 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
6 | HG00597.hp2 HG00609.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-212C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647804 | |||||||
chr11:36647828 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.359-188A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647828 | |||||||
chr11:36647887 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.359-129G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647887 | |||||||
chr11:36648228 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(163): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.498+73C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648228 | |||||||
chr11:36648380 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0133 |
2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.498+225T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648380 | |||||||
chr11:36648432 | C | T | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+277C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648432 | |||||||
chr11:36648523 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.498+368C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648523 | |||||||
chr11:36648622 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.498+467G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648622 | |||||||
chr11:36648811 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498+656C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648811 | |||||||
chr11:36648812 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0228 |
3 | HG02717.hp1 HG03486.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.498+657G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648812 | |||||||
chr11:36648825 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.498+670T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648825 | |||||||
chr11:36649005 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+850A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649005 | |||||||
chr11:36649119 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.498+964A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649119 | |||||||
chr11:36649173 | T | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+1018T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649173 | |||||||
chr11:36649199 | CA | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+1045delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649199 | |||||||
chr11:36649249 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.498+1094C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649249 | |||||||
chr11:36649354 | T | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1199T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649354 | |||||||
chr11:36649487 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.498+1332T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649487 | |||||||
chr11:36649699 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+1544G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649699 | |||||||
chr11:36649721 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498+1566C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649721 | |||||||
chr11:36649724 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+1569G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649724 | |||||||
chr11:36650111 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.498+1956C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650111 | |||||||
chr11:36650119 | G | A | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+1964G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650119 | |||||||
chr11:36650327 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.498+2172C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650327 | |||||||
chr11:36650328 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.498+2173T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650328 | |||||||
chr11:36650421 | G | A | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+2266G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650421 | |||||||
chr11:36650477 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+2322A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650477 | |||||||
chr11:36650544 | C | CT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.498+2401dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36650544 | ||||||
chr11:36650557 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0128 a0001c0001t0001g0151 |
3 | HG04115.hp1 HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.498+2402C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650557 | |||||||
chr11:36650558 | C | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+2403C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650558 | |||||||
chr11:36650559 | A | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0128 a0001c0001t0001g0151 |
3 | HG04115.hp1 HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.498+2404A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650559 | |||||||
chr11:36650613 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+2458G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650613 | |||||||
chr11:36650726 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.498+2571C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650726 | |||||||
chr11:36650743 | C | G | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+2588C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650743 | |||||||
chr11:36650768 | A | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+2613A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650768 | |||||||
chr11:36650856 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.498+2701T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650856 | |||||||
chr11:36650890 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.498+2735A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650890 | |||||||
chr11:36650930 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+2775C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650930 | |||||||
chr11:36650969 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.498+2814G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650969 | |||||||
chr11:36651005 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+2850G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651005 | |||||||
chr11:36651117 | T | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+2962T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651117 | |||||||
chr11:36651125 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(64): Show |
95 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.498+2970C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651125 | |||||||
chr11:36651150 | G | C | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0003g0013 others(3): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+2995G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651150 | |||||||
chr11:36651319 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3164G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651319 | |||||||
chr11:36651331 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3176T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651331 | |||||||
chr11:36651333 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3178T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651333 | |||||||
chr11:36651376 | G | A | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+3221G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651376 | |||||||
chr11:36651438 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3283G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651438 | |||||||
chr11:36651518 | G | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | NA18954.hp2 NA18969.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.498+3363G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651518 | |||||||
chr11:36651687 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3532T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651687 | |||||||
chr11:36651770 | T | G | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+3615T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651770 | |||||||
chr11:36651786 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.498+3631C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651786 | |||||||
chr11:36651798 | A | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.498+3643A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651798 | |||||||
chr11:36651801 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0078 others(14): Show |
24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.498+3646T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651801 | |||||||
chr11:36651985 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0229 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3830G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651985 | |||||||
chr11:36652018 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.498+3863T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652018 | |||||||
chr11:36652035 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+3880G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652035 | |||||||
chr11:36652123 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.498+3968A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652123 | |||||||
chr11:36652169 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0153 a0001c0001t0001g0183 |
4 | NA18942.hp2 NA18948.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+4014T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652169 | |||||||
chr11:36652324 | G | T | 39 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(36): Show |
47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+4169G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652324 | |||||||
chr11:36652381 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498+4226C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652381 | |||||||
chr11:36652381 | C | T | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+4226C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652381 | |||||||
chr11:36652632 | G | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+4477G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652632 | |||||||
chr11:36652782 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.498+4627A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652782 | |||||||
chr11:36652857 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.498+4702A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652857 | |||||||
chr11:36653198 | G | A | 13 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+5043G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653198 | |||||||
chr11:36653258 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+5103A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653258 | |||||||
chr11:36653270 | A | G | 1 | a0003c0006t0001g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498+5115A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653270 | |||||||
chr11:36653283 | G | C | 3 | a0002c0003t0002g0014 a0002c0004t0002g0014 a0002c0004t0002g0230 |
4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+5128G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653283 | |||||||
chr11:36653285 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.498+5130A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653285 | |||||||
chr11:36653408 | C | G | 1 | a0001c0001t0002g0054 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.498+5253C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653408 | |||||||
chr11:36653554 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.498+5399A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653554 | |||||||
chr11:36653613 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.499-5406A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653613 | |||||||
chr11:36653665 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.499-5354G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653665 | |||||||
chr11:36653718 | A | G | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-5301A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653718 | |||||||
chr11:36653864 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-5155A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653864 | |||||||
chr11:36653924 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.499-5095G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653924 | |||||||
chr11:36653963 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-5056C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653963 | |||||||
chr11:36654204 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.499-4815C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654204 | |||||||
chr11:36654343 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.499-4676T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654343 | |||||||
chr11:36654347 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-4672T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654347 | |||||||
chr11:36654353 | A | T | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-4666A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654353 | |||||||
chr11:36654387 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.499-4632T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654387 | |||||||
chr11:36654442 | C | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.499-4577C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654442 | |||||||
chr11:36654628 | C | A | 1 | a0001c0001t0002g0053 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.499-4391C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654628 | |||||||
chr11:36654669 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499-4350C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654669 | |||||||
chr11:36654720 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-4299T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654720 | |||||||
chr11:36654859 | C | T | 13 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4160C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654859 | |||||||
chr11:36654903 | C | T | 4 | a0001c0002t0003g0013 a0001c0002t0003g0203 a0001c0002t0003g0204 others(1): Show |
6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4116C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654903 | |||||||
chr11:36655106 | CTT | C | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-3910_499-3909d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36655106 | ||||||
chr11:36655367 | C | A | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-3652C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655367 | |||||||
chr11:36655504 | C | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-3515C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655504 | |||||||
chr11:36655635 | T | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-3384T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655635 | |||||||
chr11:36655689 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.499-3330G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655689 | |||||||
chr11:36655701 | T | C | 51 | a0001c0001t0001g0031 a0001c0001t0001g0135 a0001c0001t0001g0136 others(48): Show |
59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.499-3318T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655701 | |||||||
chr11:36655734 | C | T | 5 | a0001c0001t0002g0034 a0001c0001t0002g0210 a0001c0001t0002g0217 others(2): Show |
6 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3285C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655734 | |||||||
chr11:36655782 | T | G | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.499-3237T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655782 | |||||||
chr11:36655971 | A | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.499-3048A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655971 | |||||||
chr11:36655995 | A | G | 21 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(18): Show |
26 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.499-3024A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655995 | |||||||
chr11:36655996 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.499-3023T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655996 | |||||||
chr11:36656032 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.499-2987G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656032 | |||||||
chr11:36656137 | G | A | 1 | a0002c0004t0002g0230 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.499-2882G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656137 | |||||||
chr11:36656182 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-2837C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656182 | |||||||
chr11:36656398 | T | C | 11 | a0001c0001t0002g0016 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-2621T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656398 | |||||||
chr11:36656412 | A | C | 26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-2607A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656412 | |||||||
chr11:36656498 | A | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0209 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.499-2521A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656498 | |||||||
chr11:36656568 | TA | T | 39 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0032 others(36): Show |
45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.499-2440delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36656568 | ||||||
chr11:36656632 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.499-2387T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656632 | |||||||
chr11:36656650 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.499-2369G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656650 | |||||||
chr11:36656767 | T | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0141 others(8): Show |
16 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.499-2252T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656767 | |||||||
chr11:36656930 | G | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0157 a0001c0001t0001g0159 |
3 | HG02135.hp1 NA18943.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.499-2089G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656930 | |||||||
chr11:36657112 | A | T | 1 | a0001c0001t0002g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.499-1907A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657112 | |||||||
chr11:36657118 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-1901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657118 | |||||||
chr11:36657209 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.499-1810C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657209 | |||||||
chr11:36657260 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
172 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.499-1759G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657260 | |||||||
chr11:36657391 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499-1628A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657391 | |||||||
chr11:36657416 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.499-1603G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657416 | |||||||
chr11:36657423 | T | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-1596T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657423 | |||||||
chr11:36657454 | A | G | 1 | a0004c0007t0001g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.499-1565A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657454 | |||||||
chr11:36657528 | G | A | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-1491G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657528 | |||||||
chr11:36657580 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.499-1439C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657580 | |||||||
chr11:36657613 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.499-1406T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657613 | |||||||
chr11:36657655 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.499-1364C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657655 | |||||||
chr11:36657656 | C | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-1363C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657656 | |||||||
chr11:36657885 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-1134C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657885 | |||||||
chr11:36658100 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499-919G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658100 | |||||||
chr11:36658185 | T | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-834T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658185 | |||||||
chr11:36658330 | C | CT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.499-683dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36658330 | ||||||
chr11:36658356 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-663G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658356 | |||||||
chr11:36658644 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-375A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658644 | |||||||
chr11:36658675 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0115 others(2): Show |
7 | HG01884.hp2 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-344A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658675 | |||||||
chr11:36658908 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.499-111C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658908 | |||||||
chr11:36658917 | G | GA | 13 | a0001c0001t0002g0016 a0001c0001t0002g0024 a0001c0001t0002g0049 others(10): Show |
14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-96dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36658917 |