Item | Value |
---|---|
geneid | 55803 |
ensemblid | ENSG00000184060.11 |
hgncid | 16487 |
symbol | ADAP2 |
name | ArfGAP with dual PH domains 2 |
refseq_nuc | NM_018404.3 |
refseq_prot | NP_060874.1 |
ensembl_nuc | ENST00000330889.8 |
ensembl_prot | ENSP00000329468.3 |
mane_status | MANE Select |
chr | chr17 |
start | 30921945 |
end | 30959322 |
strand | + |
ver | v1.2 |
region | chr17:30921945-30959322 |
region5000 | chr17:30916945-30964322 |
regionname0 | ADAP2_chr17_30921945_30959322 |
regionname5000 | ADAP2_chr17_30916945_30964322 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 381 | 280 | 88 | 72 | 68 | 16 | 34 | 46 | ADAP2_chr17_30916945_30964322 | ADAP2 | MGDRE others(376): Show |
chr17 | 30916945 | 30964322 |
a0002 | 0/0 | 109 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | MGDRE others(104): Show |
chr17 | 30916945 | 30964322 |
a0003 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | MGDRE others(376): Show |
chr17 | 30916945 | 30964322 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1143 | 279 | 87 | 72 | 68 | 16 | 34 | ADAP2_chr17_30916945_30964322 | ADAP2 | ATGGG others(1138): Show |
chr17 | 30916945 | 30964322 | ||
a0001c0004 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | ATGGG others(1138): Show |
chr17 | 30916945 | 30964322 | ||
a0002c0003 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | ATGGG others(1138): Show |
chr17 | 30916945 | 30964322 | ||
a0003c0002 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | ATGGG others(1138): Show |
chr17 | 30916945 | 30964322 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2669 | 192 | 20 | 61 | 65 | 14 | 30 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0002 | 0/0 | 2670 | 46 | 40 | 6 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2665): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0003 | 0/0 | 2671 | 8 | 6 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2666): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0004 | 0/0 | 2669 | 6 | 6 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0005 | 0/0 | 2669 | 4 | 4 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0006 | 0/0 | 2670 | 3 | 1 | 0 | 1 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2665): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0007 | 0/0 | 2668 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2663): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0008 | 0/0 | 2669 | 2 | 0 | 0 | 0 | 1 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0009 | 0/0 | 2668 | 2 | 1 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2663): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0010 | 0/0 | 2669 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0011 | 0/0 | 2668 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2663): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0012 | 0/0 | 2669 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0013 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0014 | 0/0 | 2670 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2665): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0015 | 0/0 | 2704 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2699): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0016 | 0/0 | 2669 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0017 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0018 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0019 | 0/0 | 2669 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0001c0001t0020 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2665): Show |
chr17 | 30916945 | 30964322 |
a0001c0004t0002 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2665): Show |
chr17 | 30916945 | 30964322 |
a0002c0003t0001 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
a0003c0002t0001 | 0/0 | 2669 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | GTCCC others(2664): Show |
chr17 | 30916945 | 30964322 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 8 | 0 | 4 | 3 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0002 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0012g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0012g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0014g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0019g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0001t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0001c0004t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
a0003c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00280 | hp2 | a0001 | c0001 | t0015 | g0084 | EUR | FIN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00438 | hp2 | a0001 | c0001 | t0013 | g0106 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01261 | hp1 | a0001 | c0001 | t0012 | g0065 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01358 | hp1 | a0001 | c0001 | t0012 | g0007 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0063 | EUR | IBS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0190 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0236 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0186 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0152 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0197 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02886 | hp1 | a0001 | c0004 | t0002 | g0239 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02965 | hp1 | a0001 | c0001 | t0020 | g0025 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0078 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | ESN | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03704 | hp2 | a0001 | c0001 | t0014 | g0144 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04228 | hp1 | a0001 | c0001 | t0008 | g0120 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | YRI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA18994 | hp2 | a0003 | c0002 | t0001 | g0211 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19010 | hp1 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | YRI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ASW | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0173 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0172 | AFR | ACB | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | MSL | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | USA | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0174 | AFR | LWK | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0145 | REF | REF | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ADAP2_chr17_30916945_30964322 | ADAP2 | chr17 | 30916945 | 30964322 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30926831 | T | A | 1 | a0003 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.230T>A | p.Met77Lys | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/11 | 300/2669 | 230/1146 | 77/381 | chr17 | 30926831 | |||
chr17:30931899 | G | T | 1 | a0002 | 1 | NA18951.hp2 | stop_gained | HIGH | c.328G>T | p.Glu110* | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/11 | 398/2669 | 328/1146 | 110/381 | chr17 | 30931899 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30922074 | A | C | 1 | a0001c0004 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.60A>C | p.Thr20Thr | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 1/11 | 130/2669 | 60/1146 | 20/381 | chr17 | 30922074 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30957912 | C | A | 1 | a0001c0001t0013 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 43 | chr17 | 30957912 | ||||||
chr17:30958057 | C | T | 1 | a0001c0001t0012 | 2 | HG01261.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 188 | chr17 | 30958057 | ||||||
chr17:30958208 | C | G | 1 | a0001c0001t0020 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*339C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 339 | chr17 | 30958208 | ||||||
chr17:30958215 | T | TA | 2 | a0001c0001t0003 a0001c0001t0014 |
9 | HG01346.hp2 HG01433.hp1 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*361dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 362 | INFO_REALIGN_3_PRIME | chr17 | 30958215 | |||||
chr17:30958350 | C | CGGGCGCA others(28): Show |
1 | a0001c0001t0015 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485_*519dupCGCAGT others(29): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 520 | INFO_REALIGN_3_PRIME | chr17 | 30958350 | |||||
chr17:30958350 | C | T | 1 | a0001c0001t0019 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*481C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 481 | chr17 | 30958350 | ||||||
chr17:30958406 | G | A | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(4): Show |
65 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*537G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 537 | chr17 | 30958406 | ||||||
chr17:30958521 | A | G | 2 | a0001c0001t0011 a0001c0001t0019 |
3 | HG02280.hp1 HG02559.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*652A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 652 | chr17 | 30958521 | ||||||
chr17:30958585 | C | T | 1 | a0001c0001t0018 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*716C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 716 | chr17 | 30958585 | ||||||
chr17:30958883 | A | G | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
70 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1014A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1014 | chr17 | 30958883 | ||||||
chr17:30958887 | C | CA | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(2): Show |
59 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1032dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1033 | INFO_REALIGN_3_PRIME | chr17 | 30958887 | |||||
chr17:30958887 | CA | C | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0011 |
6 | HG02273.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1032delA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1032 | INFO_REALIGN_3_PRIME | chr17 | 30958887 | |||||
chr17:30958903 | C | G | 1 | a0001c0001t0010 | 2 | HG02257.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1034C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1034 | chr17 | 30958903 | ||||||
chr17:30959000 | G | A | 1 | a0001c0001t0017 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1131G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1131 | chr17 | 30959000 | ||||||
chr17:30959205 | T | A | 1 | a0001c0001t0008 | 2 | HG01515.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1336T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 11/11 | 1336 | chr17 | 30959205 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:30922215 | A | C | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.94+107A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 1/10 | chr17 | 30922215 | |||||||
chr17:30922236 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(93): Show |
108 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.94+128C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 1/10 | chr17 | 30922236 | |||||||
chr17:30922413 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+305G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 1/10 | chr17 | 30922413 | |||||||
chr17:30922693 | C | T | 3 | a0001c0001t0003g0241 a0001c0001t0004g0240 a0001c0004t0002g0239 |
3 | HG01433.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-247C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 1/10 | chr17 | 30922693 | |||||||
chr17:30923083 | G | C | 8 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0160 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+13G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923083 | |||||||
chr17:30923084 | C | T | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225+14C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923084 | |||||||
chr17:30923193 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.225+123G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923193 | |||||||
chr17:30923244 | C | G | 1 | a0001c0001t0003g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225+174C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923244 | |||||||
chr17:30923264 | C | CT | 31 | a0001c0001t0001g0018 a0001c0001t0001g0154 a0001c0001t0001g0155 others(28): Show |
35 | HG00597.hp1 HG00738.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.225+212dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30923264 | ||||||
chr17:30923264 | CT | C | 58 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 others(55): Show |
61 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.225+212delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30923264 | ||||||
chr17:30923264 | CTT | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.225+211_225+212del others(2): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30923264 | ||||||
chr17:30923270 | T | C | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225+200T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923270 | |||||||
chr17:30923286 | A | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+216A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923286 | |||||||
chr17:30923395 | G | T | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.225+325G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923395 | |||||||
chr17:30923413 | T | C | 16 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(13): Show |
18 | HG01433.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.225+343T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923413 | |||||||
chr17:30923475 | C | T | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.225+405C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923475 | |||||||
chr17:30923478 | T | A | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+408T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923478 | |||||||
chr17:30923560 | C | T | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225+490C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923560 | |||||||
chr17:30923562 | C | A | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.225+492C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923562 | |||||||
chr17:30923667 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.225+597C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923667 | |||||||
chr17:30923693 | C | CT | 19 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
22 | HG00597.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.225+647dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30923693 | ||||||
chr17:30923693 | CT | C | 33 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0070 others(30): Show |
35 | HG01074.hp1 HG01099.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.225+647delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30923693 | ||||||
chr17:30923811 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.225+741T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923811 | |||||||
chr17:30923835 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0026 others(3): Show |
6 | HG00741.hp1 HG01099.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+765G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923835 | |||||||
chr17:30923893 | G | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
51 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.225+823G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30923893 | |||||||
chr17:30924115 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.225+1045A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924115 | |||||||
chr17:30924132 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+1062G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924132 | |||||||
chr17:30924267 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.225+1197G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924267 | |||||||
chr17:30924370 | CA | C | 11 | a0001c0001t0001g0149 a0001c0001t0001g0166 a0001c0001t0001g0167 others(8): Show |
11 | HG01192.hp1 HG01515.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.225+1315delA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30924370 | ||||||
chr17:30924623 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(31): Show |
36 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.225+1553G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924623 | |||||||
chr17:30924646 | C | A | 9 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+1576C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924646 | |||||||
chr17:30924811 | A | T | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225+1741A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924811 | |||||||
chr17:30924812 | A | C | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.225+1742A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924812 | |||||||
chr17:30924866 | G | T | 16 | a0001c0001t0001g0163 a0001c0001t0002g0006 a0001c0001t0002g0158 others(13): Show |
18 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.225+1796G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924866 | |||||||
chr17:30924875 | G | GT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0010g0174 others(1): Show |
5 | HG01192.hp2 HG01978.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1819dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30924875 | ||||||
chr17:30924875 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0007g0162 a0001c0001t0007g0164 |
3 | HG02602.hp1 HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.225+1805G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924875 | |||||||
chr17:30924883 | T | C | 1 | a0001c0004t0002g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.225+1813T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924883 | |||||||
chr17:30924884 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.225+1814T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924884 | |||||||
chr17:30924976 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.226-1851G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30924976 | |||||||
chr17:30925033 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0157 others(40): Show |
49 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.226-1794C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925033 | |||||||
chr17:30925135 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0135 others(12): Show |
17 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.226-1692C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925135 | |||||||
chr17:30925183 | A | AT | 52 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0064 others(49): Show |
57 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.226-1624dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925183 | ||||||
chr17:30925183 | A | ATT | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
51 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.226-1625_226-1624d others(4): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925183 | ||||||
chr17:30925183 | A | ATTT | 11 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
11 | HG00140.hp2 HG01106.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.226-1626_226-1624d others(5): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925183 | ||||||
chr17:30925183 | AT | A | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0176 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.226-1624delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925183 | ||||||
chr17:30925218 | C | T | 24 | a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 others(21): Show |
28 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.226-1609C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925218 | |||||||
chr17:30925259 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.226-1568G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925259 | |||||||
chr17:30925501 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.226-1326T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925501 | |||||||
chr17:30925548 | CCTT | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0082 others(40): Show |
49 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.226-1261_226-1259d others(5): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925548 | ||||||
chr17:30925567 | CTCTTTTC others(3): Show |
C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0077 |
4 | HG00597.hp2 HG02132.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-1244_226-1235d others(12): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 30925567 | ||||||
chr17:30925685 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(24): Show |
32 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(29): Show |
intron_variant | MODIFIER | c.226-1142T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30925685 | |||||||
chr17:30926095 | C | T | 1 | a0001c0001t0004g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.226-732C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30926095 | |||||||
chr17:30926143 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0171 a0001c0001t0010g0174 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-684C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30926143 | |||||||
chr17:30926347 | A | G | 1 | a0001c0001t0011g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.226-480A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30926347 | |||||||
chr17:30926351 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.226-476G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30926351 | |||||||
chr17:30926656 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.226-171C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 2/10 | chr17 | 30926656 | |||||||
chr17:30927003 | T | G | 1 | a0001c0004t0002g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.317+85T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927003 | |||||||
chr17:30927376 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.317+458A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927376 | |||||||
chr17:30927478 | T | C | 2 | a0001c0001t0002g0075 a0001c0001t0011g0152 |
2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.317+560T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927478 | |||||||
chr17:30927534 | G | C | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+616G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927534 | |||||||
chr17:30927609 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0160 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+691C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927609 | |||||||
chr17:30927614 | C | CA | 45 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(42): Show |
49 | HG00738.hp1 HG01175.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.317+711dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30927614 | ||||||
chr17:30927626 | A | AT | 6 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0180 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+708_317+709ins others(1): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927626 | |||||||
chr17:30927627 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.317+709A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927627 | |||||||
chr17:30927908 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0083 others(5): Show |
9 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.317+990G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30927908 | |||||||
chr17:30928024 | G | GA | 9 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0002g0158 others(6): Show |
9 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+1119dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30928024 | ||||||
chr17:30928052 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.317+1134G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928052 | |||||||
chr17:30928190 | C | CA | 26 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0044 others(23): Show |
26 | HG00140.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.317+1295dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30928190 | ||||||
chr17:30928305 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0082 others(42): Show |
51 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.317+1387G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928305 | |||||||
chr17:30928312 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0171 a0001c0001t0010g0174 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+1394A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928312 | |||||||
chr17:30928330 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0003g0019 a0001c0001t0003g0228 |
4 | HG01884.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+1412T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928330 | |||||||
chr17:30928364 | T | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(44): Show |
51 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.317+1446T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928364 | |||||||
chr17:30928421 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0232 |
2 | HG01192.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.317+1503G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928421 | |||||||
chr17:30928443 | T | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(44): Show |
51 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.317+1525T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928443 | |||||||
chr17:30928576 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.317+1658C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928576 | |||||||
chr17:30928742 | G | A | 8 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0160 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+1824G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928742 | |||||||
chr17:30928761 | G | T | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.317+1843G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928761 | |||||||
chr17:30928869 | A | G | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.317+1951A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30928869 | |||||||
chr17:30929152 | G | A | 1 | a0001c0004t0002g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.317+2234G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929152 | |||||||
chr17:30929272 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.317+2354C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929272 | |||||||
chr17:30929286 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.317+2368C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929286 | |||||||
chr17:30929752 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.318-2137A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929752 | |||||||
chr17:30929761 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0126 |
2 | HG03669.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.318-2128A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929761 | |||||||
chr17:30929871 | A | G | 2 | a0001c0001t0002g0204 a0001c0001t0002g0214 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318-2018A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929871 | |||||||
chr17:30929886 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
5 | HG01192.hp2 HG01978.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.318-2003T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929886 | |||||||
chr17:30929891 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318-1998T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929891 | |||||||
chr17:30929965 | T | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(44): Show |
51 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.318-1924T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30929965 | |||||||
chr17:30930045 | C | CTTAT | 68 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.318-1805_318-1802d others(6): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30930045 | ||||||
chr17:30930045 | C | CTTATTTA others(1): Show |
15 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(12): Show |
19 | HG00280.hp2 HG00558.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.318-1809_318-1802d others(10): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30930045 | ||||||
chr17:30930045 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0001g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.318-1813_318-1802d others(14): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30930045 | ||||||
chr17:30930045 | CTTAT | C | 4 | a0001c0001t0001g0090 a0001c0001t0003g0241 a0001c0001t0004g0240 others(1): Show |
4 | HG01433.hp1 HG01496.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-1805_318-1802d others(6): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30930045 | ||||||
chr17:30930045 | CTTATTTA others(5): Show |
C | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.318-1813_318-1802d others(14): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30930045 | ||||||
chr17:30930153 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.318-1736C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930153 | |||||||
chr17:30930174 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.318-1715C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930174 | |||||||
chr17:30930255 | A | T | 1 | a0001c0001t0002g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.318-1634A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930255 | |||||||
chr17:30930261 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.318-1628G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930261 | |||||||
chr17:30930363 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0002g0053 a0001c0001t0004g0049 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.318-1526C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930363 | |||||||
chr17:30930697 | G | A | 27 | a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 others(24): Show |
31 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.318-1192G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930697 | |||||||
chr17:30930762 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.318-1127A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930762 | |||||||
chr17:30930962 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.318-927G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30930962 | |||||||
chr17:30931073 | T | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(44): Show |
51 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.318-816T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30931073 | |||||||
chr17:30931300 | C | T | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318-589C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30931300 | |||||||
chr17:30931332 | A | T | 1 | a0001c0001t0003g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.318-557A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30931332 | |||||||
chr17:30931438 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.318-451C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30931438 | |||||||
chr17:30931806 | G | T | 46 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0166 others(43): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.318-83G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | chr17 | 30931806 | |||||||
chr17:30931828 | C | CA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0163 others(8): Show |
11 | HG02630.hp2 HG02809.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.318-45dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 30931828 | ||||||
chr17:30932157 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.397+189G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932157 | |||||||
chr17:30932230 | C | CT | 13 | a0001c0001t0001g0041 a0001c0001t0001g0076 a0001c0001t0001g0079 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.397+282dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 30932230 | ||||||
chr17:30932230 | CT | C | 44 | a0001c0001t0001g0018 a0001c0001t0001g0097 a0001c0001t0001g0098 others(41): Show |
48 | HG00558.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.397+282delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 30932230 | ||||||
chr17:30932233 | T | C | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397+265T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932233 | |||||||
chr17:30932289 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.397+321G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932289 | |||||||
chr17:30932517 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.397+549G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932517 | |||||||
chr17:30932559 | CTT | C | 8 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0160 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+595_397+596del others(2): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 30932559 | ||||||
chr17:30932569 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0105 others(2): Show |
6 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+601T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932569 | |||||||
chr17:30932580 | C | CT | 5 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0208 others(2): Show |
5 | HG01433.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+626dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 30932580 | ||||||
chr17:30932580 | CT | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0168 a0001c0001t0005g0242 others(2): Show |
5 | HG00558.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+626delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 30932580 | ||||||
chr17:30932665 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0002g0158 a0001c0001t0002g0160 others(5): Show |
8 | HG02630.hp2 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+697C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932665 | |||||||
chr17:30932762 | G | T | 6 | a0001c0001t0001g0050 a0001c0001t0002g0053 a0001c0001t0004g0049 others(3): Show |
6 | HG02145.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.397+794G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932762 | |||||||
chr17:30932881 | G | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
163 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.397+913G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30932881 | |||||||
chr17:30933104 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.398-1081A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30933104 | |||||||
chr17:30933257 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0003g0057 |
2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.398-928G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30933257 | |||||||
chr17:30933568 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.398-617C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30933568 | |||||||
chr17:30933745 | G | T | 1 | a0001c0001t0014g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.398-440G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30933745 | |||||||
chr17:30933756 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398-429C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30933756 | |||||||
chr17:30934040 | T | C | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-145T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 4/10 | chr17 | 30934040 | |||||||
chr17:30934431 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG00738.hp2 HG01074.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+134C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30934431 | |||||||
chr17:30934757 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.510+460A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30934757 | |||||||
chr17:30934996 | T | G | 3 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0020g0025 |
3 | HG02717.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.510+699T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30934996 | |||||||
chr17:30935089 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0127 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.510+792G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935089 | |||||||
chr17:30935145 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.510+848T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935145 | |||||||
chr17:30935323 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.510+1026G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935323 | |||||||
chr17:30935362 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0151 |
2 | HG00741.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.510+1065C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935362 | |||||||
chr17:30935364 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0002g0071 a0001c0001t0002g0075 others(2): Show |
5 | HG01175.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+1067G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935364 | |||||||
chr17:30935541 | A | G | 48 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0230 others(45): Show |
54 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.510+1244A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935541 | |||||||
chr17:30935674 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0014g0144 |
2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.510+1377T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935674 | |||||||
chr17:30935696 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510+1399C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935696 | |||||||
chr17:30935755 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0017 others(102): Show |
117 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.510+1458T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935755 | |||||||
chr17:30935756 | G | A | 6 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0180 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+1459G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935756 | |||||||
chr17:30935761 | T | A | 27 | a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 others(24): Show |
31 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.510+1464T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935761 | |||||||
chr17:30935780 | G | T | 27 | a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 others(24): Show |
31 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.510+1483G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935780 | |||||||
chr17:30935787 | T | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0171 a0001c0001t0010g0174 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1490T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935787 | |||||||
chr17:30935940 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.510+1643T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935940 | |||||||
chr17:30935953 | A | T | 42 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0230 others(39): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+1656A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30935953 | |||||||
chr17:30936157 | C | T | 42 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0230 others(39): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+1860C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936157 | |||||||
chr17:30936180 | A | G | 42 | a0001c0001t0001g0018 a0001c0001t0001g0163 a0001c0001t0001g0230 others(39): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+1883A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936180 | |||||||
chr17:30936195 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.510+1898G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936195 | |||||||
chr17:30936291 | A | G | 5 | a0001c0001t0001g0163 a0001c0001t0003g0159 a0001c0001t0004g0161 others(2): Show |
5 | HG02809.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+1994A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936291 | |||||||
chr17:30936630 | A | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0212 |
2 | HG02129.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.510+2333A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936630 | |||||||
chr17:30936682 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(54): Show |
63 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.510+2385C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936682 | |||||||
chr17:30936920 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.510+2623T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936920 | |||||||
chr17:30936998 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0111 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.510+2701G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30936998 | |||||||
chr17:30937135 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.510+2838A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30937135 | |||||||
chr17:30937325 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.510+3028G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30937325 | |||||||
chr17:30937524 | A | T | 1 | a0001c0001t0004g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.510+3227A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30937524 | |||||||
chr17:30937653 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+3356C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30937653 | |||||||
chr17:30938059 | T | C | 2 | a0001c0001t0002g0217 a0001c0001t0003g0220 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.510+3762T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30938059 | |||||||
chr17:30938173 | A | T | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.510+3876A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30938173 | |||||||
chr17:30938350 | T | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0237 others(8): Show |
12 | HG02109.hp2 HG02145.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+4053T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30938350 | |||||||
chr17:30938603 | T | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(131): Show |
148 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+4306T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30938603 | |||||||
chr17:30939162 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
21 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.510+4865C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939162 | |||||||
chr17:30939433 | G | GA | 24 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0001g0166 others(21): Show |
25 | HG01346.hp2 HG01433.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.510+5152dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30939433 | ||||||
chr17:30939553 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.510+5256C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939553 | |||||||
chr17:30939576 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510+5279C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939576 | |||||||
chr17:30939608 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0116 a0001c0001t0001g0117 |
4 | HG00609.hp2 NA18747.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-5299A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939608 | |||||||
chr17:30939631 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.511-5276C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939631 | |||||||
chr17:30939676 | CAGG | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0237 a0001c0001t0006g0229 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-5228_511-5226d others(5): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30939676 | ||||||
chr17:30939697 | G | C | 1 | a0001c0001t0001g0005 | 3 | HG00735.hp2 HG01081.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.511-5210G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939697 | |||||||
chr17:30939762 | T | C | 80 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0101 others(77): Show |
87 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(84): Show |
intron_variant | MODIFIER | c.511-5145T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939762 | |||||||
chr17:30939771 | CA | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0104 a0001c0001t0001g0142 others(3): Show |
6 | HG00741.hp2 HG01981.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-5118delA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30939771 | ||||||
chr17:30939777 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.511-5130A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939777 | |||||||
chr17:30939864 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.511-5043A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30939864 | |||||||
chr17:30940062 | A | G | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-4845A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940062 | |||||||
chr17:30940066 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.511-4841C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940066 | |||||||
chr17:30940148 | C | T | 4 | a0001c0001t0003g0159 a0001c0001t0003g0220 a0001c0001t0003g0227 others(1): Show |
4 | HG01346.hp2 HG01433.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-4759C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940148 | |||||||
chr17:30940200 | C | T | 8 | a0001c0001t0003g0159 a0001c0001t0003g0220 a0001c0001t0003g0227 others(5): Show |
8 | HG01346.hp2 HG01433.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-4707C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940200 | |||||||
chr17:30940254 | C | T | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-4653C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940254 | |||||||
chr17:30940309 | A | ATT | 57 | a0001c0001t0001g0088 a0001c0001t0001g0231 a0001c0001t0002g0006 others(54): Show |
63 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.511-4587_511-4586d others(4): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30940309 | ||||||
chr17:30940309 | A | ATTT | 20 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(17): Show |
21 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.511-4588_511-4586d others(5): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30940309 | ||||||
chr17:30940343 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.511-4564C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940343 | |||||||
chr17:30940344 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.511-4563G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940344 | |||||||
chr17:30940556 | T | C | 80 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0101 others(77): Show |
87 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(84): Show |
intron_variant | MODIFIER | c.511-4351T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940556 | |||||||
chr17:30940585 | G | A | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.511-4322G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940585 | |||||||
chr17:30940809 | G | C | 58 | a0001c0001t0001g0088 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
64 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.511-4098G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940809 | |||||||
chr17:30940854 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0142 |
2 | HG01981.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.511-4053C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940854 | |||||||
chr17:30940887 | C | A | 5 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0180 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-4020C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30940887 | |||||||
chr17:30941066 | G | C | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.511-3841G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941066 | |||||||
chr17:30941121 | C | A | 57 | a0001c0001t0001g0088 a0001c0001t0001g0231 a0001c0001t0002g0006 others(54): Show |
63 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.511-3786C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941121 | |||||||
chr17:30941171 | G | A | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-3736G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941171 | |||||||
chr17:30941206 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.511-3701C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941206 | |||||||
chr17:30941384 | G | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(52): Show |
61 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.511-3523G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941384 | |||||||
chr17:30941545 | G | A | 55 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(52): Show |
61 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.511-3362G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941545 | |||||||
chr17:30941724 | A | G | 3 | a0001c0001t0002g0217 a0001c0001t0002g0223 a0001c0001t0002g0226 |
3 | HG01175.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.511-3183A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30941724 | |||||||
chr17:30942039 | G | C | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.511-2868G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30942039 | |||||||
chr17:30942155 | C | T | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.511-2752C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30942155 | |||||||
chr17:30942585 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.511-2322C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30942585 | |||||||
chr17:30943182 | A | T | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-1725A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943182 | |||||||
chr17:30943226 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.511-1681G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943226 | |||||||
chr17:30943280 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.511-1627G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943280 | |||||||
chr17:30943428 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0070 others(3): Show |
7 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-1479A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943428 | |||||||
chr17:30943532 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-1375T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943532 | |||||||
chr17:30943615 | G | A | 1 | a0001c0001t0010g0238 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.511-1292G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943615 | |||||||
chr17:30943776 | G | A | 2 | a0001c0001t0002g0071 a0001c0001t0002g0075 |
2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.511-1131G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943776 | |||||||
chr17:30943848 | A | AAAAT | 7 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0109 others(4): Show |
7 | HG00280.hp1 HG01993.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-1012_511-1009d others(6): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943848 | AAAAT | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(87): Show |
103 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.511-1012_511-1009d others(6): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943848 | AAAATAAA others(1): Show |
A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(61): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
intron_variant | MODIFIER | c.511-1016_511-1009d others(10): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943848 | AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
7 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-1020_511-1009d others(14): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943848 | AAAATAAA others(9): Show |
A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0142 a0001c0001t0001g0230 others(1): Show |
4 | HG01981.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-1024_511-1009d others(18): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943848 | AAAATAAA others(17): Show |
A | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-1032_511-1009d others(26): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 30943848 | ||||||
chr17:30943919 | G | A | 54 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(51): Show |
60 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.511-988G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943919 | |||||||
chr17:30943994 | C | G | 3 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0224 |
3 | HG02965.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.511-913C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30943994 | |||||||
chr17:30944000 | G | T | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.511-907G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944000 | |||||||
chr17:30944107 | G | A | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-800G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944107 | |||||||
chr17:30944142 | A | T | 1 | a0001c0001t0019g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-765A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944142 | |||||||
chr17:30944301 | A | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(160): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.511-606A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944301 | |||||||
chr17:30944337 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0231 |
2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.511-570A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944337 | |||||||
chr17:30944436 | T | C | 1 | a0001c0001t0017g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.511-471T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944436 | |||||||
chr17:30944512 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.511-395T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944512 | |||||||
chr17:30944584 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.511-323C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944584 | |||||||
chr17:30944597 | T | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-310T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944597 | |||||||
chr17:30944606 | T | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.511-301T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944606 | |||||||
chr17:30944616 | C | T | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.511-291C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944616 | |||||||
chr17:30944814 | A | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02602.hp1 HG03710.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-93A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944814 | |||||||
chr17:30944815 | T | C | 22 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(19): Show |
23 | HG01346.hp2 HG01433.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-92T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 5/10 | chr17 | 30944815 | |||||||
chr17:30945257 | G | T | 2 | a0001c0001t0011g0152 a0001c0001t0011g0236 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.657+204G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30945257 | |||||||
chr17:30945258 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.657+205C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30945258 | |||||||
chr17:30945367 | C | T | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.657+314C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30945367 | |||||||
chr17:30945848 | T | TA | 44 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(41): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.657+813dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 30945848 | ||||||
chr17:30945848 | TA | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0082 others(3): Show |
7 | HG00558.hp1 HG00639.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.657+813delA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 30945848 | ||||||
chr17:30945864 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0237 a0001c0001t0006g0229 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+811A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30945864 | |||||||
chr17:30946162 | C | CA | 10 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0166 others(7): Show |
10 | HG00621.hp1 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.657+1117dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 30946162 | ||||||
chr17:30946287 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG00738.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.657+1234C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946287 | |||||||
chr17:30946460 | C | A | 44 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(41): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.657+1407C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946460 | |||||||
chr17:30946499 | G | C | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.657+1446G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946499 | |||||||
chr17:30946760 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.657+1707T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946760 | |||||||
chr17:30946768 | C | T | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.657+1715C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946768 | |||||||
chr17:30946786 | G | T | 1 | a0001c0001t0002g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.657+1733G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30946786 | |||||||
chr17:30947096 | G | A | 2 | a0001c0001t0003g0019 a0001c0001t0003g0228 |
3 | HG01884.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.657+2043G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947096 | |||||||
chr17:30947317 | G | A | 1 | a0001c0001t0019g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-1970G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947317 | |||||||
chr17:30947434 | AC | A | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.658-1851delC | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 30947434 | ||||||
chr17:30947600 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.658-1687G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947600 | |||||||
chr17:30947677 | A | T | 1 | a0001c0001t0002g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.658-1610A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947677 | |||||||
chr17:30947719 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.658-1568C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947719 | |||||||
chr17:30947791 | A | G | 1 | a0001c0001t0019g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-1496A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30947791 | |||||||
chr17:30948026 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.658-1261C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948026 | |||||||
chr17:30948082 | T | C | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-1205T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948082 | |||||||
chr17:30948083 | G | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.658-1204G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948083 | |||||||
chr17:30948333 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.658-954C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948333 | |||||||
chr17:30948363 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02602.hp1 HG03710.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-924G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948363 | |||||||
chr17:30948408 | C | CA | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(26): Show |
35 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(32): Show |
intron_variant | MODIFIER | c.658-865dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 30948408 | ||||||
chr17:30948409 | A | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(8): Show |
12 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.658-878A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948409 | |||||||
chr17:30948410 | A | C | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.658-877A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948410 | |||||||
chr17:30948428 | C | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0228 |
3 | HG01884.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.658-859C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948428 | |||||||
chr17:30948463 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA18979.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.658-824G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948463 | |||||||
chr17:30948777 | G | T | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.658-510G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948777 | |||||||
chr17:30948788 | C | G | 1 | a0001c0001t0008g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.658-499C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948788 | |||||||
chr17:30948882 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.658-405G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948882 | |||||||
chr17:30948901 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0060 a0001c0001t0002g0171 |
5 | HG02258.hp2 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.658-386C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30948901 | |||||||
chr17:30949029 | A | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(41): Show |
50 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.658-258A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30949029 | |||||||
chr17:30949150 | C | T | 8 | a0001c0001t0004g0049 a0001c0001t0004g0054 a0001c0001t0004g0055 others(5): Show |
8 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-137C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30949150 | |||||||
chr17:30949202 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.658-85C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30949202 | |||||||
chr17:30949282 | C | T | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.658-5C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 6/10 | chr17 | 30949282 | |||||||
chr17:30949443 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0237 a0001c0001t0006g0229 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+73G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949443 | |||||||
chr17:30949545 | G | A | 4 | a0001c0001t0003g0159 a0001c0001t0003g0220 a0001c0001t0003g0227 others(1): Show |
4 | HG01346.hp2 HG01433.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+175G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949545 | |||||||
chr17:30949705 | C | T | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.741+335C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949705 | |||||||
chr17:30949748 | C | CA | 72 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(69): Show |
78 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.741+399dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 30949748 | ||||||
chr17:30949748 | C | CAA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0169 a0001c0001t0001g0237 others(3): Show |
7 | HG02109.hp2 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+398_741+399dup others(2): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 30949748 | ||||||
chr17:30949789 | T | G | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.741+419T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949789 | |||||||
chr17:30949814 | G | T | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.741+444G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949814 | |||||||
chr17:30949890 | G | A | 1 | a0001c0001t0017g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.741+520G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949890 | |||||||
chr17:30949992 | T | C | 3 | a0001c0001t0010g0174 a0001c0001t0010g0238 a0001c0001t0016g0078 |
3 | HG02257.hp2 HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.741+622T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30949992 | |||||||
chr17:30950096 | T | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.741+726T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950096 | |||||||
chr17:30950331 | A | G | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.741+961A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950331 | |||||||
chr17:30950334 | C | T | 8 | a0001c0001t0004g0049 a0001c0001t0004g0054 a0001c0001t0004g0055 others(5): Show |
8 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+964C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950334 | |||||||
chr17:30950471 | C | T | 55 | a0001c0001t0001g0107 a0001c0001t0002g0006 a0001c0001t0002g0012 others(52): Show |
61 | HG00621.hp2 HG00738.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.741+1101C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950471 | |||||||
chr17:30950503 | C | T | 1 | a0001c0001t0019g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741+1133C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950503 | |||||||
chr17:30950778 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.741+1408T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950778 | |||||||
chr17:30950794 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.741+1424A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950794 | |||||||
chr17:30950819 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0062 a0001c0001t0001g0076 others(3): Show |
7 | HG02132.hp1 HG03669.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+1449C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950819 | |||||||
chr17:30950912 | G | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.741+1542G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30950912 | |||||||
chr17:30951058 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.741+1688A>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951058 | |||||||
chr17:30951271 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.741+1901C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951271 | |||||||
chr17:30951498 | A | T | 17 | a0001c0001t0001g0018 a0001c0001t0001g0138 a0001c0001t0001g0166 others(14): Show |
18 | HG01074.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.742-1790A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951498 | |||||||
chr17:30951508 | A | T | 75 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(72): Show |
82 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(79): Show |
intron_variant | MODIFIER | c.742-1780A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951508 | |||||||
chr17:30951558 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.742-1730A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951558 | |||||||
chr17:30951654 | C | CT | 5 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0134 others(2): Show |
5 | HG00621.hp1 HG01109.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-1615dupT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 30951654 | ||||||
chr17:30951654 | CTTT | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0237 a0001c0001t0002g0006 others(65): Show |
75 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(72): Show |
intron_variant | MODIFIER | c.742-1617_742-1615d others(5): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 30951654 | ||||||
chr17:30951654 | CTTTT | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-1618_742-1615d others(6): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 30951654 | ||||||
chr17:30951662 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.742-1626T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951662 | |||||||
chr17:30951719 | C | G | 4 | a0001c0001t0003g0159 a0001c0001t0003g0220 a0001c0001t0003g0227 others(1): Show |
4 | HG01346.hp2 HG01433.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-1569C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951719 | |||||||
chr17:30951724 | T | C | 4 | a0001c0001t0003g0159 a0001c0001t0003g0220 a0001c0001t0003g0227 others(1): Show |
4 | HG01346.hp2 HG01433.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-1564T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951724 | |||||||
chr17:30951803 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
14 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.742-1485T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951803 | |||||||
chr17:30951817 | G | A | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.742-1471G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951817 | |||||||
chr17:30951856 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.742-1432C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951856 | |||||||
chr17:30951866 | A | G | 1 | a0001c0001t0006g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.742-1422A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951866 | |||||||
chr17:30951950 | T | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.742-1338T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951950 | |||||||
chr17:30951957 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.742-1331A>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951957 | |||||||
chr17:30951987 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.742-1301C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30951987 | |||||||
chr17:30952226 | T | C | 2 | a0001c0001t0004g0049 a0001c0001t0004g0059 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.742-1062T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952226 | |||||||
chr17:30952367 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.742-921C>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952367 | |||||||
chr17:30952497 | T | C | 58 | a0001c0001t0002g0006 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
64 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.742-791T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952497 | |||||||
chr17:30952520 | C | T | 1 | a0001c0001t0009g0190 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.742-768C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952520 | |||||||
chr17:30952522 | C | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(13): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.742-766C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952522 | |||||||
chr17:30952658 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.742-630G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952658 | |||||||
chr17:30952907 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
5 | HG00738.hp2 HG01106.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.742-381T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30952907 | |||||||
chr17:30953019 | T | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.742-269T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30953019 | |||||||
chr17:30953179 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.742-109C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30953179 | |||||||
chr17:30953246 | T | C | 1 | a0001c0001t0017g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.742-42T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30953246 | |||||||
chr17:30953262 | G | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(13): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.742-26G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 7/10 | chr17 | 30953262 | |||||||
chr17:30953383 | TGGTTTAA others(28): Show |
T | 1 | a0001c0001t0015g0084 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.804+36_804+70delTT others(33): Show |
ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 30953383 | ||||||
chr17:30953403 | G | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+53G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953403 | |||||||
chr17:30953423 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0060 a0001c0001t0002g0171 |
5 | HG02258.hp2 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+73G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953423 | |||||||
chr17:30953428 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.804+78T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953428 | |||||||
chr17:30953619 | C | T | 1 | a0001c0001t0016g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.804+269C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953619 | |||||||
chr17:30953655 | G | A | 3 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0005g0244 |
3 | HG03209.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.804+305G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953655 | |||||||
chr17:30953690 | C | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0066 others(1): Show |
4 | HG00642.hp2 HG01106.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+340C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953690 | |||||||
chr17:30953879 | AT | A | 74 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(71): Show |
81 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(78): Show |
intron_variant | MODIFIER | c.804+541delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 30953879 | ||||||
chr17:30953894 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.804+544C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953894 | |||||||
chr17:30953928 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.805-550G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30953928 | |||||||
chr17:30954047 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.805-431T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30954047 | |||||||
chr17:30954049 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.805-429T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30954049 | |||||||
chr17:30954406 | T | C | 3 | a0001c0001t0011g0152 a0001c0001t0011g0236 a0001c0001t0019g0172 |
3 | HG02280.hp1 HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.805-72T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 8/10 | chr17 | 30954406 | |||||||
chr17:30954677 | T | C | 1 | a0002c0003t0001g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.882+122T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30954677 | |||||||
chr17:30954678 | T | A | 1 | a0002c0003t0001g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.882+123T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30954678 | |||||||
chr17:30954836 | T | G | 1 | a0001c0001t0005g0215 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+281T>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30954836 | |||||||
chr17:30954896 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0231 |
2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.882+341C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30954896 | |||||||
chr17:30954955 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.882+400T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30954955 | |||||||
chr17:30955113 | AT | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.882+571delT | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 30955113 | ||||||
chr17:30955278 | T | TA | 7 | a0001c0001t0002g0053 a0001c0001t0002g0158 a0001c0001t0002g0160 others(4): Show |
7 | HG02486.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+735dupA | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 30955278 | ||||||
chr17:30955563 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.883-678C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30955563 | |||||||
chr17:30955567 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0077 |
3 | HG02132.hp1 NA18952.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.883-674C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30955567 | |||||||
chr17:30955632 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.883-609G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30955632 | |||||||
chr17:30955695 | C | T | 1 | a0001c0001t0011g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.883-546C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30955695 | |||||||
chr17:30955863 | C | T | 1 | a0001c0001t0019g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.883-378C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30955863 | |||||||
chr17:30956127 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.883-114T>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 9/10 | chr17 | 30956127 | |||||||
chr17:30956585 | C | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0015 others(9): Show |
16 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111+116C>G | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956585 | |||||||
chr17:30956654 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1111+185G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956654 | |||||||
chr17:30956676 | C | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0050 others(11): Show |
16 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111+207C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956676 | |||||||
chr17:30956758 | G | A | 8 | a0001c0001t0004g0049 a0001c0001t0004g0054 a0001c0001t0004g0055 others(5): Show |
8 | HG02145.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1111+289G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956758 | |||||||
chr17:30956784 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0009g0197 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1111+315C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956784 | |||||||
chr17:30956840 | T | C | 2 | a0001c0001t0011g0152 a0001c0001t0011g0236 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1111+371T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956840 | |||||||
chr17:30956906 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111+437T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30956906 | |||||||
chr17:30957012 | G | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.1111+543G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957012 | |||||||
chr17:30957018 | C | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(13): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111+549C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957018 | |||||||
chr17:30957196 | T | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0001t0001g0167 others(73): Show |
83 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(80): Show |
intron_variant | MODIFIER | c.1112-639T>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957196 | |||||||
chr17:30957257 | C | T | 10 | a0001c0001t0001g0128 a0001c0001t0001g0183 a0001c0001t0001g0185 others(7): Show |
10 | HG00642.hp1 HG01070.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1112-578C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957257 | |||||||
chr17:30957390 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1112-445G>A | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957390 | |||||||
chr17:30957432 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1112-403A>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957432 | |||||||
chr17:30957454 | G | T | 2 | a0001c0001t0010g0174 a0001c0001t0010g0238 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1112-381G>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957454 | |||||||
chr17:30957490 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0237 a0001c0001t0006g0229 |
4 | HG02109.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1112-345C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957490 | |||||||
chr17:30957645 | G | C | 4 | a0001c0001t0005g0215 a0001c0001t0005g0242 a0001c0001t0005g0243 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1112-190G>C | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957645 | |||||||
chr17:30957689 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1112-146C>T | ADAP2 | ENSG00000184060.11 | transcript | ENST00000330889.8 | protein_coding | 10/10 | chr17 | 30957689 |