Item | Value |
---|---|
geneid | 5074 |
ensemblid | ENSG00000177425.11 |
hgncid | 8614 |
symbol | PAWR |
name | pro-apoptotic WT1 regulator |
refseq_nuc | NM_002583.4 |
refseq_prot | NP_002574.2 |
ensembl_nuc | ENST00000328827.9 |
ensembl_prot | ENSP00000328088.4 |
mane_status | MANE Select |
chr | chr12 |
start | 79584879 |
end | 79690964 |
strand | - |
ver | v1.2 |
region | chr12:79584879-79690964 |
region5000 | chr12:79579879-79695964 |
regionname0 | PAWR_chr12_79584879_79690964 |
regionname5000 | PAWR_chr12_79579879_79695964 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 340 | 156 | 17 | 33 | 84 | 2 | 18 | 65 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0002 | 0/0 | 340 | 82 | 36 | 8 | 31 | 0 | 7 | 27 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0003 | 0/0 | 340 | 11 | 8 | 2 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0004 | 0/0 | 340 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0005 | 0/0 | 340 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0006 | 0/0 | 340 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
a0007 | 0/0 | 340 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | MATGG others(335): Show |
chr12 | 79579879 | 79695964 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1020 | 107 | 16 | 25 | 53 | 2 | 10 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0001c0003 | 1/0 | 1020 | 49 | 1 | 8 | 31 | 0 | 8 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0002c0002 | 0/0 | 1020 | 82 | 36 | 8 | 31 | 0 | 7 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0003c0004 | 0/0 | 1020 | 8 | 5 | 2 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0003c0005 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0004c0006 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0005c0007 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0006c0008 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 | ||
a0007c0009 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ATGGC others(1015): Show |
chr12 | 79579879 | 79695964 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 8987 | 57 | 1 | 15 | 33 | 1 | 6 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8982): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0003 | 0/0 | 8991 | 5 | 3 | 0 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0004 | 0/0 | 8991 | 30 | 9 | 6 | 11 | 1 | 3 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0006 | 0/0 | 8990 | 6 | 1 | 3 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8985): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0010 | 0/0 | 8991 | 3 | 0 | 0 | 3 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0016 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0025 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8983): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0026 | 0/0 | 8988 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8983): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0029 | 0/0 | 8987 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8982): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0030 | 0/0 | 8987 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8982): Show |
chr12 | 79579879 | 79695964 |
a0001c0001t0032 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0002 | 0/0 | 8987 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8982): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0003 | 1/0 | 8991 | 35 | 1 | 8 | 20 | 0 | 5 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0008 | 0/0 | 8991 | 5 | 0 | 0 | 5 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0013 | 0/0 | 8991 | 2 | 0 | 0 | 2 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0014 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0023 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0024 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8987): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0027 | 0/0 | 8992 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8987): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0028 | 0/0 | 8991 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0001c0003t0031 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0001 | 0/0 | 8991 | 61 | 21 | 5 | 29 | 0 | 6 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0005 | 0/0 | 8991 | 13 | 10 | 3 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0012 | 0/0 | 8992 | 2 | 0 | 0 | 1 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8987): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0015 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0017 | 0/0 | 8992 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8987): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0018 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0019 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0020 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0002c0002t0021 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0003c0004t0001 | 0/0 | 8991 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0003c0004t0007 | 0/0 | 8991 | 2 | 1 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0003c0004t0009 | 0/0 | 8989 | 4 | 3 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8984): Show |
chr12 | 79579879 | 79695964 |
a0003c0004t0022 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0003c0005t0007 | 0/0 | 8991 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0004c0006t0011 | 0/0 | 8992 | 3 | 3 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8987): Show |
chr12 | 79579879 | 79695964 |
a0005c0007t0033 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0005c0007t0034 | 0/0 | 8991 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0006c0008t0003 | 0/0 | 8991 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
a0007c0009t0003 | 0/0 | 8991 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | ACTTT others(8986): Show |
chr12 | 79579879 | 79695964 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0016g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0025g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0026g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0029g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0030g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0001t0032g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0014g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0023g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0024g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0027g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0028g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0001c0003t0031g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0017g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0018g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0019g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0002c0002t0021g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0004t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0003c0005t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0004c0006t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0005c0007t0033g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0005c0007t0034g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0006c0008t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
a0007c0009t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00423 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0141 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00621 | hp1 | a0001 | c0003 | t0003 | g0077 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00639 | hp2 | a0002 | c0002 | t0005 | g0181 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG00741 | hp2 | a0001 | c0003 | t0003 | g0099 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01069 | hp2 | a0001 | c0003 | t0003 | g0082 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0086 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01074 | hp2 | a0003 | c0004 | t0009 | g0159 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01099 | hp1 | a0001 | c0003 | t0003 | g0006 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01109 | hp1 | a0002 | c0002 | t0005 | g0247 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01169 | hp1 | a0006 | c0008 | t0003 | g0097 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01243 | hp1 | a0003 | c0004 | t0007 | g0166 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01261 | hp1 | a0002 | c0002 | t0005 | g0251 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01261 | hp2 | a0001 | c0003 | t0003 | g0095 | AMR | CLM | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0182 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0102 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01928 | hp1 | a0001 | c0003 | t0003 | g0098 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0045 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01975 | hp1 | a0001 | c0001 | t0030 | g0058 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01981 | hp2 | a0001 | c0003 | t0003 | g0078 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0013 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02055 | hp2 | a0002 | c0002 | t0005 | g0232 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02056 | hp1 | a0001 | c0001 | t0025 | g0109 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0145 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02071 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02145 | hp1 | a0005 | c0007 | t0033 | g0255 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02257 | hp1 | a0002 | c0002 | t0017 | g0183 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02258 | hp1 | a0004 | c0006 | t0011 | g0239 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02451 | hp2 | a0003 | c0004 | t0022 | g0165 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02523 | hp1 | a0001 | c0003 | t0013 | g0094 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02602 | hp1 | a0001 | c0003 | t0028 | g0083 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02615 | hp1 | a0002 | c0002 | t0015 | g0176 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02622 | hp2 | a0002 | c0002 | t0005 | g0243 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0242 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02683 | hp1 | a0001 | c0003 | t0003 | g0144 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02717 | hp2 | a0002 | c0002 | t0005 | g0249 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02886 | hp1 | a0002 | c0002 | t0021 | g0185 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02895 | hp2 | a0002 | c0002 | t0005 | g0213 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02896 | hp1 | a0003 | c0004 | t0009 | g0157 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02896 | hp2 | a0002 | c0002 | t0005 | g0250 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02922 | hp1 | a0003 | c0004 | t0007 | g0167 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02922 | hp2 | a0003 | c0005 | t0007 | g0164 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02976 | hp1 | a0005 | c0007 | t0034 | g0254 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03041 | hp2 | a0002 | c0002 | t0018 | g0244 | AFR | GWD | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0248 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03195 | hp2 | a0003 | c0004 | t0009 | g0156 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03209 | hp2 | a0002 | c0002 | t0019 | g0178 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03225 | hp1 | a0004 | c0006 | t0011 | g0238 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03453 | hp1 | a0003 | c0005 | t0007 | g0004 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03486 | hp2 | a0004 | c0006 | t0011 | g0240 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03490 | hp2 | a0001 | c0003 | t0003 | g0093 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0208 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03491 | hp2 | a0007 | c0009 | t0003 | g0151 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | ESN | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03654 | hp1 | a0001 | c0001 | t0029 | g0119 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03831 | hp2 | a0001 | c0003 | t0027 | g0134 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03927 | hp1 | a0002 | c0002 | t0012 | g0188 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03927 | hp2 | a0001 | c0003 | t0003 | g0253 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04115 | hp1 | a0001 | c0003 | t0024 | g0148 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0224 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04184 | hp1 | a0001 | c0003 | t0003 | g0096 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04228 | hp1 | a0001 | c0003 | t0003 | g0142 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | STU | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18939 | hp1 | a0001 | c0003 | t0003 | g0081 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18941 | hp2 | a0001 | c0001 | t0026 | g0055 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18942 | hp2 | a0001 | c0003 | t0014 | g0161 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18946 | hp1 | a0001 | c0003 | t0008 | g0135 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18956 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18957 | hp1 | a0001 | c0003 | t0023 | g0147 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18959 | hp2 | a0001 | c0003 | t0031 | g0121 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18960 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18966 | hp2 | a0001 | c0003 | t0008 | g0137 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0130 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18967 | hp2 | a0002 | c0002 | t0012 | g0220 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18968 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18969 | hp1 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18972 | hp1 | a0001 | c0003 | t0008 | g0150 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18982 | hp2 | a0001 | c0003 | t0008 | g0136 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18984 | hp1 | a0001 | c0003 | t0008 | g0138 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18985 | hp1 | a0001 | c0003 | t0013 | g0040 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18987 | hp2 | a0001 | c0001 | t0010 | g0128 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19001 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19002 | hp1 | a0001 | c0003 | t0003 | g0131 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0143 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19007 | hp2 | a0001 | c0003 | t0003 | g0100 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19056 | hp2 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19060 | hp2 | a0001 | c0003 | t0003 | g0101 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19065 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19066 | hp1 | a0002 | c0002 | t0020 | g0193 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19079 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19084 | hp1 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19085 | hp1 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0132 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0074 | EAS | JPT | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19240 | hp1 | a0002 | c0002 | t0005 | g0246 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA19240 | hp2 | a0003 | c0005 | t0007 | g0163 | AFR | YRI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0016 | EUR | TSI | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02486 | hp1 | a0002 | c0002 | t0005 | g0245 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG03471 | hp2 | a0003 | c0004 | t0009 | g0158 | AFR | MSL | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG06807 | hp1 | a0001 | c0001 | t0032 | g0007 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | USA | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0129 | REF | REF | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0105 | REF | REF | PAWR_chr12_79579879_79695964 | PAWR | chr12 | 79579879 | 79695964 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79596633 | C | A | 1 | a0006 | 1 | HG01169.hp1 | missense_variant | MODERATE | c.709G>T | p.Val237Phe | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/7 | 949/8991 | 709/1023 | 237/340 | chr12 | 79596633 | |||
chr12:79621127 | A | C | 4 | a0002 a0003 a0004 others(1): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
missense_variant | MODERATE | c.597T>G | p.Ile199Met | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 837/8991 | 597/1023 | 199/340 | chr12 | 79621127 | |||
chr12:79621147 | T | C | 1 | a0007 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.577A>G | p.Ile193Val | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 817/8991 | 577/1023 | 193/340 | chr12 | 79621147 | |||
chr12:79689874 | T | C | 1 | a0005 | 2 | HG02145.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.371A>G | p.Gln124Arg | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 611/8991 | 371/1023 | 124/340 | chr12 | 79689874 | |||
chr12:79690012 | G | C | 1 | a0002 | 82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
missense_variant | MODERATE | c.233C>G | p.Pro78Arg | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 473/8991 | 233/1023 | 78/340 | chr12 | 79690012 | |||
chr12:79690120 | G | A | 1 | a0004 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.125C>T | p.Pro42Leu | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/7 | 365/8991 | 125/1023 | 42/340 | chr12 | 79690120 | |||
chr12:79690874 | T | C | 1 | a0005 | 2 | HG02145.hp1 HG02976.hp1 |
splice_region_variant | LOW | c.-150A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/7 | chr12 | 79690874 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79592625 | C | A | 3 | a0003c0005 a0004c0006 a0005c0007 |
8 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(5): Show |
synonymous_variant | LOW | c.1005G>T | p.Val335Val | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1245/8991 | 1005/1023 | 335/340 | chr12 | 79592625 | |||
chr12:79621127 | A | T | 1 | a0001c0001 | 106 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
synonymous_variant | LOW | c.597T>A | p.Ile199Ile | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/7 | 837/8991 | 597/1023 | 199/340 | chr12 | 79621127 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79584919 | TAA | T | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7686_*7687delTT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7686 | chr12 | 79584919 | ||||||
chr12:79585275 | G | A | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7332C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7332 | chr12 | 79585275 | ||||||
chr12:79585294 | G | A | 1 | a0001c0001t0030 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7313C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7313 | chr12 | 79585294 | ||||||
chr12:79585414 | G | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7193C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7193 | chr12 | 79585414 | ||||||
chr12:79585415 | A | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7192T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7192 | chr12 | 79585415 | ||||||
chr12:79585535 | C | T | 1 | a0002c0002t0020 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7072G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 7072 | chr12 | 79585535 | ||||||
chr12:79585610 | C | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6997G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6997 | chr12 | 79585610 | ||||||
chr12:79585791 | G | C | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6816C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6816 | chr12 | 79585791 | ||||||
chr12:79586003 | C | T | 1 | a0001c0001t0025 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6604G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6604 | chr12 | 79586003 | ||||||
chr12:79586043 | C | T | 1 | a0001c0001t0029 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6564 | chr12 | 79586043 | ||||||
chr12:79586083 | C | T | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6524G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6524 | chr12 | 79586083 | ||||||
chr12:79586092 | A | G | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6515T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6515 | chr12 | 79586092 | ||||||
chr12:79586139 | A | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6468T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6468 | chr12 | 79586139 | ||||||
chr12:79586166 | C | T | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6441G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 6441 | chr12 | 79586166 | ||||||
chr12:79586925 | C | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5682G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5682 | chr12 | 79586925 | ||||||
chr12:79587035 | G | A | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5572C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5572 | chr12 | 79587035 | ||||||
chr12:79587262 | G | A | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5345C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 5345 | chr12 | 79587262 | ||||||
chr12:79587908 | GCTGT | G | 6 | a0001c0001t0002 a0001c0001t0025 a0001c0001t0026 others(3): Show |
61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*4695_*4698delACAG | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4695 | chr12 | 79587908 | ||||||
chr12:79587948 | G | C | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4659C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4659 | chr12 | 79587948 | ||||||
chr12:79588074 | C | A | 1 | a0001c0003t0013 | 2 | HG02523.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4533G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4533 | chr12 | 79588074 | ||||||
chr12:79588199 | C | T | 1 | a0001c0001t0016 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4408G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4408 | chr12 | 79588199 | ||||||
chr12:79588272 | A | G | 1 | a0001c0003t0028 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4335T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4335 | chr12 | 79588272 | ||||||
chr12:79588487 | T | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4120A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4120 | chr12 | 79588487 | ||||||
chr12:79588511 | A | C | 1 | a0001c0001t0032 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4096T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 4096 | chr12 | 79588511 | ||||||
chr12:79588722 | T | A | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3885A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3885 | chr12 | 79588722 | ||||||
chr12:79588797 | C | T | 2 | a0001c0003t0027 a0001c0003t0031 |
2 | HG03831.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3810G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3810 | chr12 | 79588797 | ||||||
chr12:79588909 | G | C | 3 | a0001c0003t0008 a0001c0003t0027 a0001c0003t0031 |
7 | HG03831.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3698C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3698 | chr12 | 79588909 | ||||||
chr12:79588916 | C | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3691G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3691 | chr12 | 79588916 | ||||||
chr12:79589262 | G | C | 1 | a0005c0007t0034 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3345C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3345 | chr12 | 79589262 | ||||||
chr12:79589274 | A | G | 1 | a0003c0004t0009 | 4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3333T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3333 | chr12 | 79589274 | ||||||
chr12:79589496 | T | C | 1 | a0002c0002t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3111A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3111 | chr12 | 79589496 | ||||||
chr12:79589527 | T | G | 1 | a0001c0001t0032 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3080A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 3080 | chr12 | 79589527 | ||||||
chr12:79589734 | T | C | 1 | a0002c0002t0018 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2873A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2873 | chr12 | 79589734 | ||||||
chr12:79589935 | C | T | 1 | a0004c0006t0011 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2672G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2672 | chr12 | 79589935 | ||||||
chr12:79590196 | A | AT | 10 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0016 others(7): Show |
44 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2410dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2410 | chr12 | 79590196 | ||||||
chr12:79590246 | C | G | 1 | a0002c0002t0019 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2361G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2361 | chr12 | 79590246 | ||||||
chr12:79590389 | C | T | 3 | a0002c0002t0005 a0002c0002t0017 a0002c0002t0018 |
15 | HG00639.hp2 HG01109.hp1 HG01261.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2218G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2218 | chr12 | 79590389 | ||||||
chr12:79590447 | C | T | 1 | a0001c0001t0010 | 3 | NA18968.hp2 NA18987.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2160G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2160 | chr12 | 79590447 | ||||||
chr12:79590515 | AT | A | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2091delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2091 | chr12 | 79590515 | ||||||
chr12:79590539 | T | C | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2068A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 2068 | chr12 | 79590539 | ||||||
chr12:79590908 | T | A | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1699A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1699 | chr12 | 79590908 | ||||||
chr12:79590919 | C | T | 10 | a0002c0002t0001 a0002c0002t0005 a0002c0002t0012 others(7): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1688G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1688 | chr12 | 79590919 | ||||||
chr12:79591014 | C | T | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1593G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1593 | chr12 | 79591014 | ||||||
chr12:79591146 | A | G | 1 | a0002c0002t0015 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1461 | chr12 | 79591146 | ||||||
chr12:79591540 | C | T | 2 | a0005c0007t0033 a0005c0007t0034 |
2 | HG02145.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 1067 | chr12 | 79591540 | ||||||
chr12:79591616 | G | A | 1 | a0003c0004t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*991C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 991 | chr12 | 79591616 | ||||||
chr12:79591895 | C | T | 1 | a0001c0003t0023 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 712 | chr12 | 79591895 | ||||||
chr12:79592094 | A | C | 21 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(18): Show |
138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*513T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 513 | chr12 | 79592094 | ||||||
chr12:79592224 | G | T | 1 | a0001c0003t0014 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 7/7 | 383 | chr12 | 79592224 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:79592875 | G | A | 137 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(134): Show |
138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.937-182C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79592875 | |||||||
chr12:79592919 | T | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.937-226A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79592919 | |||||||
chr12:79593068 | T | C | 2 | a0001c0003t0003g0099 a0001c0003t0003g0102 |
2 | HG00741.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.937-375A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593068 | |||||||
chr12:79593069 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.937-376T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593069 | |||||||
chr12:79593166 | A | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.937-473T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593166 | |||||||
chr12:79593454 | A | G | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.937-761T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593454 | |||||||
chr12:79593666 | T | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+663A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593666 | |||||||
chr12:79593701 | G | A | 38 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(35): Show |
39 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.936+628C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | |||||||
chr12:79593701 | G | GT | 37 | a0001c0001t0002g0065 a0001c0001t0002g0068 a0001c0001t0002g0092 others(34): Show |
37 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.936+627dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | |||||||
chr12:79593701 | G | T | 1 | a0001c0001t0004g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.936+628C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593701 | |||||||
chr12:79593740 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0025g0109 |
2 | HG02056.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.936+589G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593740 | |||||||
chr12:79593793 | C | T | 1 | a0003c0004t0009g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.936+536G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593793 | |||||||
chr12:79593892 | C | T | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.936+437G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593892 | |||||||
chr12:79593914 | G | C | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.936+415C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79593914 | |||||||
chr12:79594048 | A | G | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+281T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79594048 | |||||||
chr12:79594234 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936+95A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 6/6 | chr12 | 79594234 | |||||||
chr12:79594567 | T | C | 1 | a0003c0004t0009g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.832-134A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594567 | |||||||
chr12:79594700 | C | CGT | 12 | a0001c0001t0002g0060 a0001c0001t0002g0067 a0001c0003t0023g0147 others(9): Show |
12 | HG01074.hp2 HG01243.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.832-269_832-268dup others(2): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | |||||||
chr12:79594700 | C | CGTGTGTG others(5): Show |
1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-279_832-268dup others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | |||||||
chr12:79594700 | C | CGTGTGTG others(7): Show |
1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.832-281_832-268dup others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | |||||||
chr12:79594700 | CGT | C | 34 | a0001c0001t0002g0111 a0001c0001t0002g0114 a0001c0001t0004g0001 others(31): Show |
35 | HG00423.hp2 HG00438.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.832-269_832-268del others(2): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | |||||||
chr12:79594700 | CGTGTGTG others(5): Show |
C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.832-279_832-268del others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594700 | |||||||
chr12:79594744 | T | G | 7 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0124 others(4): Show |
7 | HG02040.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-311A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79594744 | |||||||
chr12:79595114 | T | C | 1 | a0001c0003t0003g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.832-681A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595114 | |||||||
chr12:79595393 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.832-960A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595393 | |||||||
chr12:79595617 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+894G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595617 | |||||||
chr12:79595646 | A | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+865T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79595646 | |||||||
chr12:79596174 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.831+337G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596174 | |||||||
chr12:79596295 | A | G | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.831+216T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596295 | |||||||
chr12:79596430 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.831+81A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 5/6 | chr12 | 79596430 | |||||||
chr12:79596713 | C | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-55G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79596713 | |||||||
chr12:79597057 | C | CT | 7 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0003t0003g0086 others(4): Show |
7 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.684-400dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597057 | |||||||
chr12:79597144 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.684-486C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597144 | |||||||
chr12:79597354 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-696C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597354 | |||||||
chr12:79597426 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.684-768A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597426 | |||||||
chr12:79597711 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.684-1053T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597711 | |||||||
chr12:79597751 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1093T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597751 | |||||||
chr12:79597816 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1158T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597816 | |||||||
chr12:79597880 | T | C | 1 | a0001c0003t0003g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.684-1222A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597880 | |||||||
chr12:79597971 | G | A | 131 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(128): Show |
132 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.684-1313C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79597971 | |||||||
chr12:79598003 | A | G | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-1345T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598003 | |||||||
chr12:79598017 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-1359A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598017 | |||||||
chr12:79598256 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.684-1598A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598256 | |||||||
chr12:79598413 | A | G | 2 | a0002c0002t0001g0214 a0002c0002t0001g0241 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.684-1755T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598413 | |||||||
chr12:79598607 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.684-1949T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598607 | |||||||
chr12:79598851 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-2193G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79598851 | |||||||
chr12:79599033 | C | T | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.684-2375G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599033 | |||||||
chr12:79599149 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.684-2491A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599149 | |||||||
chr12:79599162 | A | G | 1 | a0001c0001t0004g0028 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.684-2504T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599162 | |||||||
chr12:79599924 | C | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-3266G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599924 | |||||||
chr12:79599925 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.684-3267C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599925 | |||||||
chr12:79599940 | A | G | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-3282T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599940 | |||||||
chr12:79599992 | T | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-3334A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79599992 | |||||||
chr12:79600026 | G | T | 1 | a0003c0004t0009g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.684-3368C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600026 | |||||||
chr12:79600259 | A | G | 1 | a0002c0002t0001g0219 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.684-3601T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600259 | |||||||
chr12:79600478 | G | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-3820C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600478 | |||||||
chr12:79600486 | G | A | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.684-3828C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600486 | |||||||
chr12:79600488 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.684-3830C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600488 | |||||||
chr12:79600535 | C | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.684-3877G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600535 | |||||||
chr12:79600616 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-3958C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600616 | |||||||
chr12:79600648 | C | CT | 78 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0080 others(75): Show |
78 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.684-3991dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | |||||||
chr12:79600648 | C | CTT | 9 | a0002c0002t0001g0169 a0002c0002t0001g0189 a0002c0002t0001g0190 others(6): Show |
9 | HG01256.hp1 HG01261.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.684-3992_684-3991d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | |||||||
chr12:79600648 | CT | C | 9 | a0001c0001t0006g0022 a0003c0004t0007g0166 a0003c0004t0007g0167 others(6): Show |
9 | HG01074.hp2 HG01168.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-3991delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | |||||||
chr12:79600648 | CTT | C | 6 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.684-3992_684-3991d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600648 | |||||||
chr12:79600770 | A | G | 1 | a0001c0003t0003g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.684-4112T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600770 | |||||||
chr12:79600958 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.684-4300T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79600958 | |||||||
chr12:79601207 | A | AT | 12 | a0001c0001t0002g0049 a0001c0001t0002g0054 a0001c0001t0002g0075 others(9): Show |
12 | HG01243.hp2 HG01981.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.684-4550dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | |||||||
chr12:79601207 | AT | A | 40 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0010 others(37): Show |
40 | HG00423.hp2 HG01074.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.684-4550delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | |||||||
chr12:79601207 | ATT | A | 18 | a0001c0001t0004g0001 a0001c0001t0004g0016 a0001c0001t0004g0020 others(15): Show |
19 | HG00621.hp2 HG01074.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.684-4551_684-4550d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | |||||||
chr12:79601207 | ATTT | A | 74 | a0001c0001t0006g0015 a0002c0002t0001g0168 a0002c0002t0001g0171 others(71): Show |
74 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.684-4552_684-4550d others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601207 | |||||||
chr12:79601551 | T | G | 1 | a0001c0001t0004g0023 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.684-4893A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601551 | |||||||
chr12:79601907 | G | A | 3 | a0002c0002t0005g0182 a0002c0002t0005g0232 a0002c0002t0017g0183 |
3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.684-5249C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601907 | |||||||
chr12:79601908 | C | A | 3 | a0002c0002t0005g0182 a0002c0002t0005g0232 a0002c0002t0017g0183 |
3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.684-5250G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601908 | |||||||
chr12:79601999 | A | T | 2 | a0002c0002t0001g0175 a0002c0002t0001g0179 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.684-5341T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79601999 | |||||||
chr12:79602056 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-5398T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602056 | |||||||
chr12:79602135 | C | T | 1 | a0003c0005t0007g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.684-5477G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602135 | |||||||
chr12:79602213 | G | A | 1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.684-5555C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602213 | |||||||
chr12:79602348 | T | G | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.684-5690A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602348 | |||||||
chr12:79602770 | A | AT | 10 | a0001c0001t0002g0041 a0001c0001t0002g0052 a0001c0001t0002g0152 others(7): Show |
10 | HG00639.hp2 HG01891.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.684-6113dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79602770 | |||||||
chr12:79603153 | G | A | 1 | a0001c0001t0006g0024 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.684-6495C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603153 | |||||||
chr12:79603314 | C | G | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-6656G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603314 | |||||||
chr12:79603320 | CAAATAAG others(6): Show |
C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-6675_684-6663d others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603320 | |||||||
chr12:79603367 | A | G | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02523.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.684-6709T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603367 | |||||||
chr12:79603541 | C | T | 1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.684-6883G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603541 | |||||||
chr12:79603584 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.684-6926A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603584 | |||||||
chr12:79603665 | C | CAATTTTT others(4): Show |
1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.684-7008_684-7007i others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603665 | |||||||
chr12:79603666 | T | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-7008A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603666 | |||||||
chr12:79603667 | A | AT | 25 | a0001c0001t0002g0043 a0001c0001t0002g0050 a0001c0001t0002g0052 others(22): Show |
25 | HG00423.hp1 HG00438.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.684-7010dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | |||||||
chr12:79603667 | A | T | 4 | a0001c0003t0013g0040 a0001c0003t0013g0094 a0005c0007t0033g0255 others(1): Show |
4 | HG02145.hp1 HG02523.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.684-7009T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | |||||||
chr12:79603667 | AT | A | 82 | a0001c0001t0002g0005 a0001c0001t0002g0072 a0001c0001t0004g0001 others(79): Show |
83 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-7010delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | |||||||
chr12:79603667 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0029g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.684-7025_684-7010d others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79603667 | |||||||
chr12:79604174 | T | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.684-7516A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604174 | |||||||
chr12:79604834 | TAGAAAAC | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.684-8183_684-8177d others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604834 | |||||||
chr12:79604857 | G | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.684-8199C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79604857 | |||||||
chr12:79605018 | C | T | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-8360G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605018 | |||||||
chr12:79605020 | G | A | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.684-8362C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605020 | |||||||
chr12:79605047 | GATA | G | 4 | a0002c0002t0001g0171 a0002c0002t0001g0211 a0002c0002t0001g0212 others(1): Show |
4 | HG03139.hp1 HG03209.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.684-8392_684-8390d others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605047 | |||||||
chr12:79605060 | A | ATATAT | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.684-8403_684-8402i others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605060 | |||||||
chr12:79605090 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.684-8432A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605090 | |||||||
chr12:79605529 | T | A | 59 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0043 others(56): Show |
59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.683+8046A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605529 | |||||||
chr12:79605530 | A | T | 90 | a0001c0001t0006g0009 a0002c0002t0001g0168 a0002c0002t0001g0169 others(87): Show |
90 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.683+8045T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605530 | |||||||
chr12:79605531 | A | T | 4 | a0002c0002t0001g0218 a0003c0005t0007g0004 a0003c0005t0007g0163 others(1): Show |
4 | HG02922.hp2 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+8044T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605531 | |||||||
chr12:79605620 | G | A | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+7955C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605620 | |||||||
chr12:79605690 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7885T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605690 | |||||||
chr12:79605758 | T | C | 1 | a0001c0003t0003g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.683+7817A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605758 | |||||||
chr12:79605768 | C | T | 1 | a0002c0002t0005g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.683+7807G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605768 | |||||||
chr12:79605847 | C | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7728G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605847 | |||||||
chr12:79605919 | C | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.683+7656G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79605919 | |||||||
chr12:79606058 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.683+7517T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606058 | |||||||
chr12:79606397 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+7178A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606397 | |||||||
chr12:79606789 | T | C | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.683+6786A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606789 | |||||||
chr12:79606969 | C | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6606G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79606969 | |||||||
chr12:79607153 | G | A | 2 | a0001c0001t0002g0063 a0001c0001t0002g0071 |
2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.683+6422C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607153 | |||||||
chr12:79607310 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6265A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607310 | |||||||
chr12:79607423 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+6152G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607423 | |||||||
chr12:79607587 | G | A | 2 | a0001c0003t0003g0006 a0001c0003t0028g0083 |
2 | HG01099.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.683+5988C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607587 | |||||||
chr12:79607711 | G | A | 1 | a0001c0001t0004g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683+5864C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607711 | |||||||
chr12:79607728 | CA | C | 67 | a0001c0001t0002g0046 a0001c0001t0002g0052 a0001c0001t0002g0054 others(64): Show |
68 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.683+5846delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607728 | |||||||
chr12:79607734 | A | T | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5841T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607734 | |||||||
chr12:79607739 | A | T | 81 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(78): Show |
81 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.683+5836T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607739 | |||||||
chr12:79607743 | A | T | 18 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0006g0009 others(15): Show |
18 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.683+5832T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607743 | |||||||
chr12:79607744 | A | T | 88 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(85): Show |
88 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.683+5831T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607744 | |||||||
chr12:79607745 | AT | A | 33 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0047 others(30): Show |
33 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.683+5829delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607745 | |||||||
chr12:79607746 | T | A | 107 | a0001c0001t0002g0043 a0001c0001t0002g0089 a0001c0001t0002g0113 others(104): Show |
107 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.683+5829A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607746 | |||||||
chr12:79607878 | C | T | 1 | a0002c0002t0001g0236 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.683+5697G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607878 | |||||||
chr12:79607879 | G | A | 1 | a0002c0002t0019g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683+5696C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607879 | |||||||
chr12:79607887 | C | T | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+5688G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607887 | |||||||
chr12:79607894 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0073 |
2 | HG01069.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.683+5681T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607894 | |||||||
chr12:79607912 | G | A | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5663C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607912 | |||||||
chr12:79607980 | C | T | 1 | a0002c0002t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.683+5595G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607980 | |||||||
chr12:79607990 | A | C | 2 | a0001c0003t0003g0078 a0001c0003t0003g0101 |
2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.683+5585T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79607990 | |||||||
chr12:79608002 | T | C | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.683+5573A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608002 | |||||||
chr12:79608033 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+5542C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608033 | |||||||
chr12:79608044 | G | A | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.683+5531C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608044 | |||||||
chr12:79608049 | C | CA | 12 | a0001c0001t0002g0047 a0001c0001t0002g0059 a0001c0001t0002g0075 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.683+5525dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608049 | |||||||
chr12:79608326 | G | A | 141 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(138): Show |
142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.683+5249C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608326 | |||||||
chr12:79608418 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+5157C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608418 | |||||||
chr12:79608453 | C | T | 3 | a0001c0001t0002g0050 a0001c0001t0002g0092 a0001c0001t0002g0118 |
3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.683+5122G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79608453 | |||||||
chr12:79609008 | A | G | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.683+4567T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609008 | |||||||
chr12:79609052 | G | A | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.683+4523C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609052 | |||||||
chr12:79609429 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+4146G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609429 | |||||||
chr12:79609601 | A | G | 5 | a0001c0003t0008g0135 a0001c0003t0008g0136 a0001c0003t0008g0137 others(2): Show |
5 | NA18946.hp1 NA18966.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.683+3974T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609601 | |||||||
chr12:79609614 | G | T | 1 | a0001c0003t0003g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.683+3961C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609614 | |||||||
chr12:79609647 | T | C | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.683+3928A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609647 | |||||||
chr12:79609720 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+3855C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609720 | |||||||
chr12:79609784 | C | T | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.683+3791G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609784 | |||||||
chr12:79609790 | G | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+3785C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609790 | |||||||
chr12:79609891 | CT | C | 4 | a0001c0003t0002g0154 a0001c0003t0003g0085 a0001c0003t0003g0130 others(1): Show |
4 | NA18967.hp1 NA18969.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+3683delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79609891 | |||||||
chr12:79610086 | C | T | 1 | a0002c0002t0019g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.683+3489G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610086 | |||||||
chr12:79610098 | T | TG | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+3476dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610098 | |||||||
chr12:79610208 | T | C | 1 | a0002c0002t0018g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.683+3367A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610208 | |||||||
chr12:79610538 | C | T | 1 | a0001c0003t0003g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.683+3037G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610538 | |||||||
chr12:79610539 | G | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.683+3036C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610539 | |||||||
chr12:79610694 | G | C | 1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.683+2881C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610694 | |||||||
chr12:79610735 | T | C | 3 | a0002c0002t0001g0171 a0002c0002t0001g0211 a0002c0002t0001g0212 |
3 | HG03139.hp1 NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.683+2840A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610735 | |||||||
chr12:79610762 | TA | T | 7 | a0001c0001t0002g0005 a0001c0001t0002g0118 a0001c0001t0004g0026 others(4): Show |
7 | HG01257.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.683+2812delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610762 | |||||||
chr12:79610808 | A | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+2767T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610808 | |||||||
chr12:79610903 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+2672G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610903 | |||||||
chr12:79610922 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+2653C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610922 | |||||||
chr12:79610995 | A | T | 1 | a0001c0001t0003g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683+2580T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79610995 | |||||||
chr12:79611019 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0062 |
2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.683+2556T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611019 | |||||||
chr12:79611087 | T | G | 3 | a0002c0002t0005g0182 a0002c0002t0005g0232 a0002c0002t0017g0183 |
3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.683+2488A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611087 | |||||||
chr12:79611390 | C | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+2185G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611390 | |||||||
chr12:79611797 | T | C | 1 | a0002c0002t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.683+1778A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611797 | |||||||
chr12:79611881 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.683+1694T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611881 | |||||||
chr12:79611992 | A | G | 1 | a0002c0002t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.683+1583T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79611992 | |||||||
chr12:79612111 | G | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683+1464C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612111 | |||||||
chr12:79612324 | CTCTT | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+1247_683+1250d others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612324 | |||||||
chr12:79612349 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+1226A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612349 | |||||||
chr12:79612367 | A | G | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.683+1208T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612367 | |||||||
chr12:79612477 | A | C | 4 | a0001c0003t0002g0154 a0001c0003t0003g0085 a0001c0003t0003g0130 others(1): Show |
4 | NA18967.hp1 NA18969.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.683+1098T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612477 | |||||||
chr12:79612570 | A | G | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.683+1005T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612570 | |||||||
chr12:79612729 | G | C | 2 | a0001c0001t0004g0010 a0001c0001t0004g0011 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.683+846C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612729 | |||||||
chr12:79612738 | C | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+837G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612738 | |||||||
chr12:79612866 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+709T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612866 | |||||||
chr12:79612913 | G | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.683+662C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79612913 | |||||||
chr12:79613236 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683+339A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613236 | |||||||
chr12:79613391 | A | G | 1 | a0002c0002t0001g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.683+184T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613391 | |||||||
chr12:79613411 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.683+164G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613411 | |||||||
chr12:79613548 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683+27T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 4/6 | chr12 | 79613548 | |||||||
chr12:79613718 | G | A | 3 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0124 |
3 | HG02040.hp2 HG02080.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.649-109C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613718 | |||||||
chr12:79613899 | T | C | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649-290A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613899 | |||||||
chr12:79613931 | T | TTATATA | 4 | a0001c0001t0002g0043 a0001c0001t0002g0122 a0001c0001t0002g0133 others(1): Show |
4 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-328_649-323dup others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613931 | T | TTATATAT others(3): Show |
1 | a0001c0003t0003g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.649-332_649-323dup others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613931 | T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.649-334_649-323dup others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613931 | T | TTATATAT others(7): Show |
1 | a0001c0003t0008g0150 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.649-336_649-323dup others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613931 | T | TTATATAT others(11): Show |
1 | a0001c0003t0003g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.649-340_649-323dup others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613931 | TTATATAT others(15): Show |
T | 1 | a0001c0003t0003g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.649-344_649-323del others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613931 | |||||||
chr12:79613933 | A | T | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.649-324T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613933 | |||||||
chr12:79613943 | ATATATAT others(38): Show |
A | 1 | a0001c0001t0002g0071 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.649-379_649-335del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | |||||||
chr12:79613943 | ATATATAT others(41): Show |
A | 1 | a0001c0001t0002g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.649-382_649-335del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | |||||||
chr12:79613943 | ATATATAT others(48): Show |
A | 4 | a0001c0001t0004g0012 a0001c0001t0004g0123 a0001c0001t0004g0124 others(1): Show |
4 | HG01109.hp2 HG02683.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-389_649-335del others(55): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | |||||||
chr12:79613943 | ATATATAT others(49): Show |
A | 23 | a0001c0001t0004g0002 a0001c0001t0004g0010 a0001c0001t0004g0011 others(20): Show |
23 | HG01081.hp2 HG01099.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.649-390_649-335del others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | |||||||
chr12:79613943 | ATATATAT others(50): Show |
A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0127 |
2 | HG02976.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.649-391_649-335del others(57): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613943 | |||||||
chr12:79613945 | ATATATAT others(39): Show |
A | 1 | a0001c0003t0003g0139 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.649-382_649-337del others(46): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | |||||||
chr12:79613945 | ATATATAT others(40): Show |
A | 1 | a0001c0003t0028g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.649-383_649-337del others(47): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | |||||||
chr12:79613945 | ATATATAT others(48): Show |
A | 1 | a0001c0001t0004g0035 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.649-391_649-337del others(55): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | |||||||
chr12:79613945 | ATATATAT others(49): Show |
A | 8 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0023 others(5): Show |
9 | HG01257.hp2 HG01258.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.649-392_649-337del others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613945 | |||||||
chr12:79613947 | ATATATAT others(34): Show |
A | 1 | a0002c0002t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.649-379_649-339del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | |||||||
chr12:79613947 | ATATATAT others(35): Show |
A | 1 | a0001c0003t0003g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.649-380_649-339del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | |||||||
chr12:79613947 | ATATATAT others(38): Show |
A | 1 | a0001c0001t0002g0064 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.649-383_649-339del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | |||||||
chr12:79613947 | ATATATAT others(41): Show |
A | 1 | a0001c0001t0002g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-386_649-339del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | |||||||
chr12:79613947 | ATATATAT others(47): Show |
A | 1 | a0001c0001t0004g0155 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.649-392_649-339del others(54): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613947 | |||||||
chr12:79613949 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0020g0193 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.649-378_649-341del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | |||||||
chr12:79613949 | ATATATAT others(32): Show |
A | 1 | a0002c0002t0001g0217 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.649-379_649-341del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | |||||||
chr12:79613949 | ATATATAT others(44): Show |
A | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.649-391_649-341del others(51): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613949 | |||||||
chr12:79613951 | ATATATAT others(29): Show |
A | 1 | a0002c0002t0001g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.649-378_649-343del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(30): Show |
A | 1 | a0001c0001t0002g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.649-379_649-343del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(31): Show |
A | 3 | a0001c0001t0002g0152 a0002c0002t0001g0194 a0002c0002t0001g0235 |
3 | HG00673.hp2 HG04204.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.649-380_649-343del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(32): Show |
A | 3 | a0001c0001t0002g0106 a0001c0001t0002g0115 a0002c0002t0001g0197 |
3 | NA18987.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.649-381_649-343del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(33): Show |
A | 1 | a0002c0002t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.649-382_649-343del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(34): Show |
A | 5 | a0001c0003t0003g0099 a0002c0002t0001g0173 a0002c0002t0001g0191 others(2): Show |
5 | HG00741.hp2 HG03490.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-383_649-343del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(35): Show |
A | 1 | a0002c0002t0001g0172 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.649-384_649-343del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(41): Show |
A | 1 | a0003c0004t0007g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.649-390_649-343del others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613951 | ATATATAT others(42): Show |
A | 1 | a0003c0004t0007g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.649-391_649-343del others(49): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613951 | |||||||
chr12:79613953 | ATATATAT others(28): Show |
A | 1 | a0002c0002t0001g0234 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.649-379_649-345del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613953 | ATATATAT others(29): Show |
A | 2 | a0002c0002t0001g0215 a0002c0002t0019g0178 |
2 | HG00544.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.649-380_649-345del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613953 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0012g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.649-382_649-345del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613953 | ATATATAT others(32): Show |
A | 3 | a0002c0002t0001g0190 a0002c0002t0005g0248 a0002c0002t0005g0251 |
3 | HG01261.hp1 HG02027.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.649-383_649-345del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613953 | ATATATAT others(34): Show |
A | 5 | a0002c0002t0001g0195 a0002c0002t0001g0219 a0002c0002t0001g0225 others(2): Show |
5 | NA18946.hp2 NA18965.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-385_649-345del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613953 | ATATATAT others(35): Show |
A | 1 | a0002c0002t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.649-386_649-345del others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613953 | |||||||
chr12:79613955 | ATATATAT others(29): Show |
A | 2 | a0002c0002t0001g0230 a0002c0002t0001g0231 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.649-382_649-347del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613955 | ATATATAT others(30): Show |
A | 2 | a0002c0002t0001g0177 a0002c0002t0001g0228 |
2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.649-383_649-347del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613955 | ATATATAT others(31): Show |
A | 2 | a0002c0002t0001g0174 a0002c0002t0001g0186 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.649-384_649-347del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613955 | ATATATAT others(32): Show |
A | 12 | a0001c0001t0032g0007 a0002c0002t0001g0169 a0002c0002t0001g0192 others(9): Show |
12 | HG02572.hp1 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-385_649-347del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613955 | ATATATAT others(33): Show |
A | 2 | a0002c0002t0001g0241 a0002c0002t0005g0213 |
2 | HG02895.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.649-386_649-347del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613955 | ATATATAT others(34): Show |
A | 3 | a0002c0002t0001g0237 a0002c0002t0021g0185 a0003c0004t0001g0008 |
3 | HG02071.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.649-387_649-347del others(41): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613955 | |||||||
chr12:79613957 | ATATATAT others(26): Show |
A | 1 | a0001c0003t0008g0135 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.649-381_649-349del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0026g0055 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.649-382_649-349del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(28): Show |
A | 4 | a0002c0002t0001g0175 a0002c0002t0001g0179 a0002c0002t0001g0212 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-383_649-349del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(29): Show |
A | 4 | a0002c0002t0001g0187 a0002c0002t0001g0201 a0002c0002t0001g0211 others(1): Show |
4 | NA19003.hp1 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-384_649-349del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(30): Show |
A | 3 | a0002c0002t0001g0227 a0002c0002t0001g0229 a0002c0002t0005g0181 |
3 | HG00639.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.649-385_649-349del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0005g0232 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.649-386_649-349del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(32): Show |
A | 7 | a0002c0002t0001g0170 a0002c0002t0001g0184 a0002c0002t0005g0182 others(4): Show |
7 | HG01192.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-387_649-349del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613957 | ATATATAT others(33): Show |
A | 2 | a0002c0002t0005g0245 a0002c0002t0005g0247 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.649-388_649-349del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613957 | |||||||
chr12:79613959 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0002g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.649-379_649-351del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.649-380_649-351del others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(27): Show |
A | 1 | a0001c0001t0002g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.649-384_649-351del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(28): Show |
A | 1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.649-385_649-351del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(29): Show |
A | 5 | a0002c0002t0001g0189 a0002c0002t0001g0202 a0002c0002t0001g0204 others(2): Show |
5 | HG00621.hp2 HG02300.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-386_649-351del others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(30): Show |
A | 3 | a0002c0002t0001g0180 a0002c0002t0001g0207 a0002c0002t0017g0183 |
3 | HG01975.hp2 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.649-387_649-351del others(37): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(31): Show |
A | 1 | a0002c0002t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.649-388_649-351del others(38): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(33): Show |
A | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.649-390_649-351del others(40): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613959 | ATATATAT others(38): Show |
A | 1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.649-395_649-351del others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613959 | |||||||
chr12:79613961 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.649-383_649-353del others(31): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | |||||||
chr12:79613961 | ATATATAT others(27): Show |
A | 2 | a0001c0003t0003g0084 a0002c0002t0001g0203 |
2 | HG02071.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.649-386_649-353del others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | |||||||
chr12:79613961 | ATATATAT others(28): Show |
A | 1 | a0004c0006t0011g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.649-387_649-353del others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | |||||||
chr12:79613961 | ATATATAT others(32): Show |
A | 1 | a0002c0002t0005g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.649-391_649-353del others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613961 | |||||||
chr12:79613963 | ATATATAT others(25): Show |
A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.649-386_649-355del others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613963 | |||||||
chr12:79613963 | ATATATAT others(26): Show |
A | 1 | a0002c0002t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.649-387_649-355del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613963 | |||||||
chr12:79613965 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.649-379_649-357del others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | |||||||
chr12:79613965 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0002g0092 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.649-382_649-357del others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | |||||||
chr12:79613965 | ATATATAT others(24): Show |
A | 2 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.649-387_649-357del others(31): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | |||||||
chr12:79613965 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0003g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.649-388_649-357del others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613965 | |||||||
chr12:79613967 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.649-377_649-359del others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | |||||||
chr12:79613967 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.649-379_649-359del others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | |||||||
chr12:79613967 | ATATATAT others(17): Show |
A | 1 | a0001c0003t0008g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.649-382_649-359del others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613967 | |||||||
chr12:79613969 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0042 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.649-382_649-361del others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | |||||||
chr12:79613969 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0002g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.649-387_649-361del others(27): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | |||||||
chr12:79613969 | ATATATAT others(26): Show |
A | 1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.649-393_649-361del others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613969 | |||||||
chr12:79613973 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.649-378_649-365del others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | |||||||
chr12:79613973 | ATATATAT others(18): Show |
A | 1 | a0003c0004t0009g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.649-389_649-365del others(25): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | |||||||
chr12:79613973 | ATATATAT others(22): Show |
A | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.649-393_649-365del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613973 | |||||||
chr12:79613975 | A | T | 1 | a0003c0004t0009g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.649-366T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | |||||||
chr12:79613975 | ATATATTT others(6): Show |
A | 1 | a0001c0003t0003g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.649-379_649-367del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | |||||||
chr12:79613975 | ATATATTT others(8): Show |
A | 1 | a0001c0001t0002g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.649-381_649-367del others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | |||||||
chr12:79613975 | ATATATTT others(11): Show |
A | 1 | a0001c0003t0024g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.649-384_649-367del others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613975 | |||||||
chr12:79613977 | A | T | 1 | a0003c0004t0009g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.649-368T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613977 | ATATTTTT others(3): Show |
A | 1 | a0001c0001t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.649-378_649-369del others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613977 | ATATTTTT others(4): Show |
A | 3 | a0001c0001t0002g0060 a0001c0001t0029g0119 a0001c0001t0030g0058 |
3 | HG01952.hp1 HG01975.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.649-379_649-369del others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613977 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0002g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.649-381_649-369del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613977 | ATATTTTT others(8): Show |
A | 1 | a0001c0001t0002g0005 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.649-383_649-369del others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613977 | ATATTTTT others(9): Show |
A | 1 | a0001c0003t0003g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.649-384_649-369del others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613977 | |||||||
chr12:79613979 | A | T | 2 | a0001c0001t0003g0108 a0003c0004t0009g0157 |
2 | HG02896.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.649-370T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTT | A | 5 | a0001c0001t0002g0091 a0001c0003t0003g0142 a0001c0003t0003g0146 others(2): Show |
5 | HG04228.hp1 NA18939.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-373_649-371del others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0002g0054 a0001c0001t0002g0104 a0001c0001t0002g0113 others(3): Show |
6 | HG00639.hp1 HG01074.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-378_649-371del others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0002g0062 a0001c0001t0002g0107 a0001c0001t0002g0111 others(4): Show |
7 | HG00438.hp1 HG01891.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-380_649-371del others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(4): Show |
A | 7 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0059 others(4): Show |
7 | HG01081.hp1 HG01192.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.649-381_649-371del others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0057 a0006c0008t0003g0097 |
2 | HG01169.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.649-382_649-371del others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(6): Show |
A | 1 | a0003c0004t0009g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.649-383_649-371del others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613979 | ATTTTTTT others(22): Show |
A | 1 | a0001c0003t0003g0006 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.649-399_649-371del others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613979 | |||||||
chr12:79613980 | T | TA | 4 | a0001c0001t0002g0069 a0001c0003t0003g0140 a0001c0003t0027g0134 others(1): Show |
4 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-372_649-371ins others(1): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | |||||||
chr12:79613980 | T | TATA | 3 | a0001c0001t0002g0066 a0001c0003t0003g0081 a0001c0003t0003g0103 |
3 | HG01255.hp2 NA18939.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.649-372_649-371ins others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | |||||||
chr12:79613980 | T | TATATATA others(4): Show |
1 | a0001c0003t0003g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.649-372_649-371ins others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613980 | |||||||
chr12:79613981 | T | A | 10 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0061 others(7): Show |
10 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.649-372A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613981 | |||||||
chr12:79613982 | T | A | 12 | a0001c0001t0002g0069 a0001c0001t0002g0076 a0001c0001t0002g0090 others(9): Show |
12 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-373A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613982 | |||||||
chr12:79613983 | T | A | 11 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0061 others(8): Show |
11 | HG00544.hp1 HG00673.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.649-374A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613983 | |||||||
chr12:79613984 | T | A | 16 | a0001c0001t0002g0069 a0001c0001t0002g0076 a0001c0001t0002g0090 others(13): Show |
16 | HG02040.hp1 HG03491.hp2 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.649-375A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613984 | |||||||
chr12:79613985 | T | A | 12 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0061 others(9): Show |
12 | HG00544.hp1 HG00673.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.649-376A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613985 | |||||||
chr12:79613986 | T | A | 19 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0076 others(16): Show |
19 | HG01069.hp2 HG02040.hp1 HG03491.hp2 others(16): Show |
intron_variant | MODIFIER | c.649-377A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613986 | |||||||
chr12:79613987 | T | A | 15 | a0001c0001t0002g0043 a0001c0001t0002g0056 a0001c0001t0002g0061 others(12): Show |
15 | HG00544.hp1 HG00673.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.649-378A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613987 | |||||||
chr12:79613988 | T | A | 20 | a0001c0001t0002g0065 a0001c0001t0002g0067 a0001c0001t0002g0069 others(17): Show |
20 | HG00438.hp2 HG00621.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-379A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613988 | |||||||
chr12:79613989 | T | A | 20 | a0001c0001t0002g0043 a0001c0001t0002g0054 a0001c0001t0002g0056 others(17): Show |
20 | HG00639.hp1 HG00673.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-380A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613989 | |||||||
chr12:79613990 | T | A | 22 | a0001c0001t0002g0065 a0001c0001t0002g0069 a0001c0001t0002g0076 others(19): Show |
22 | HG00438.hp2 HG00621.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.649-381A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613990 | |||||||
chr12:79613991 | T | A | 24 | a0001c0001t0002g0043 a0001c0001t0002g0054 a0001c0001t0002g0061 others(21): Show |
24 | HG00438.hp1 HG00639.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.649-382A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613991 | |||||||
chr12:79613992 | T | A | 20 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0069 others(17): Show |
20 | HG00621.hp1 HG01192.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.649-383A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613992 | |||||||
chr12:79613993 | T | A | 14 | a0001c0001t0002g0043 a0001c0001t0002g0061 a0001c0001t0002g0068 others(11): Show |
14 | HG00639.hp1 HG00673.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-384A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613993 | |||||||
chr12:79613994 | T | A | 8 | a0001c0001t0002g0069 a0001c0001t0002g0091 a0001c0003t0003g0096 others(5): Show |
8 | HG02040.hp1 HG03471.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.649-385A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613994 | |||||||
chr12:79613995 | T | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0104 a0001c0003t0008g0150 |
3 | HG00639.hp1 HG02074.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.649-386A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613995 | |||||||
chr12:79613996 | T | A | 4 | a0001c0001t0002g0091 a0001c0003t0027g0134 a0001c0003t0031g0121 others(1): Show |
4 | HG03471.hp2 HG03831.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-387A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79613996 | |||||||
chr12:79614001 | T | A | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.649-392A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614001 | |||||||
chr12:79614010 | T | C | 1 | a0002c0002t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.649-401A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614010 | |||||||
chr12:79614044 | C | G | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-435G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614044 | |||||||
chr12:79614063 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.649-454A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614063 | |||||||
chr12:79614088 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-479C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614088 | |||||||
chr12:79614103 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.649-494G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614103 | |||||||
chr12:79614312 | A | ATAGTCTT | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-710_649-704dup others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614312 | |||||||
chr12:79614763 | G | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.649-1154C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614763 | |||||||
chr12:79614795 | T | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.649-1186A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79614795 | |||||||
chr12:79615291 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.649-1682G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615291 | |||||||
chr12:79615469 | C | T | 1 | a0002c0002t0001g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.649-1860G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615469 | |||||||
chr12:79615470 | G | T | 1 | a0002c0002t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.649-1861C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615470 | |||||||
chr12:79615572 | C | A | 1 | a0002c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.649-1963G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615572 | |||||||
chr12:79615657 | G | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-2048C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615657 | |||||||
chr12:79615662 | C | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-2053G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615662 | |||||||
chr12:79615828 | G | T | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.649-2219C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615828 | |||||||
chr12:79615914 | G | A | 1 | a0001c0003t0003g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.649-2305C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79615914 | |||||||
chr12:79616056 | C | CA | 86 | a0001c0001t0002g0071 a0001c0001t0002g0075 a0001c0001t0002g0153 others(83): Show |
86 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.649-2448dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616056 | |||||||
chr12:79616056 | CA | C | 10 | a0001c0001t0002g0063 a0001c0001t0002g0107 a0001c0001t0002g0115 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.649-2448delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616056 | |||||||
chr12:79616193 | A | T | 14 | a0003c0004t0007g0166 a0003c0004t0007g0167 a0003c0004t0009g0156 others(11): Show |
14 | HG01074.hp2 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-2584T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616193 | |||||||
chr12:79616389 | A | T | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.649-2780T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616389 | |||||||
chr12:79616428 | T | G | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-2819A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616428 | |||||||
chr12:79616674 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.649-3065C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616674 | |||||||
chr12:79616676 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.649-3067G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616676 | |||||||
chr12:79616680 | T | C | 1 | a0002c0002t0020g0193 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.649-3071A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616680 | |||||||
chr12:79616789 | C | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.649-3180G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616789 | |||||||
chr12:79616839 | C | A | 1 | a0003c0004t0009g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.649-3230G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616839 | |||||||
chr12:79616861 | C | T | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649-3252G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79616861 | |||||||
chr12:79617586 | A | AG | 141 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(138): Show |
142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.648+3489dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617586 | |||||||
chr12:79617628 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.648+3448A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617628 | |||||||
chr12:79617782 | T | G | 3 | a0002c0002t0005g0182 a0002c0002t0005g0232 a0002c0002t0017g0183 |
3 | HG01884.hp2 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.648+3294A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617782 | |||||||
chr12:79617884 | G | C | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+3192C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79617884 | |||||||
chr12:79618032 | C | A | 3 | a0001c0001t0002g0050 a0001c0001t0002g0092 a0001c0001t0002g0118 |
3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.648+3044G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618032 | |||||||
chr12:79618130 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+2946A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618130 | |||||||
chr12:79618202 | G | C | 8 | a0001c0003t0003g0045 a0001c0003t0003g0082 a0001c0003t0003g0086 others(5): Show |
8 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.648+2874C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618202 | |||||||
chr12:79618429 | C | T | 1 | a0001c0003t0003g0006 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.648+2647G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618429 | |||||||
chr12:79618549 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.648+2527A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618549 | |||||||
chr12:79618902 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+2174A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618902 | |||||||
chr12:79618963 | C | T | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.648+2113G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79618963 | |||||||
chr12:79619181 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1895G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619181 | |||||||
chr12:79619252 | G | A | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.648+1824C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619252 | |||||||
chr12:79619429 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1647A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619429 | |||||||
chr12:79619479 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+1597C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619479 | |||||||
chr12:79619580 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.648+1496C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619580 | |||||||
chr12:79619588 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.648+1488T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619588 | |||||||
chr12:79619710 | C | T | 1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.648+1366G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619710 | |||||||
chr12:79619729 | G | A | 1 | a0001c0001t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.648+1347C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619729 | |||||||
chr12:79619878 | C | T | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.648+1198G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619878 | |||||||
chr12:79619935 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.648+1141A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79619935 | |||||||
chr12:79620392 | G | C | 1 | a0002c0002t0005g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648+684C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620392 | |||||||
chr12:79620408 | A | G | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.648+668T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620408 | |||||||
chr12:79620528 | C | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.648+548G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620528 | |||||||
chr12:79620593 | T | C | 15 | a0002c0002t0001g0187 a0002c0002t0001g0189 a0002c0002t0001g0190 others(12): Show |
15 | HG00621.hp2 HG01975.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.648+483A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620593 | |||||||
chr12:79620744 | A | G | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.648+332T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620744 | |||||||
chr12:79620979 | G | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.648+97C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79620979 | |||||||
chr12:79621066 | A | C | 1 | a0001c0003t0003g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.648+10T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 3/6 | chr12 | 79621066 | |||||||
chr12:79621406 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-199G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621406 | |||||||
chr12:79621593 | A | C | 1 | a0002c0002t0005g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-386T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621593 | |||||||
chr12:79621756 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-549A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621756 | |||||||
chr12:79621779 | G | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-572C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621779 | |||||||
chr12:79621793 | G | A | 203 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(200): Show |
204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.517-586C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621793 | |||||||
chr12:79621813 | C | T | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-606G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621813 | |||||||
chr12:79621989 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-782A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79621989 | |||||||
chr12:79622308 | A | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-1101T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622308 | |||||||
chr12:79622482 | A | G | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1275T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622482 | |||||||
chr12:79622576 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-1369A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622576 | |||||||
chr12:79622579 | T | C | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-1372A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622579 | |||||||
chr12:79622632 | A | G | 1 | a0001c0003t0003g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-1425T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622632 | |||||||
chr12:79622941 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-1734C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622941 | |||||||
chr12:79622987 | T | C | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-1780A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79622987 | |||||||
chr12:79623068 | T | C | 2 | a0001c0003t0003g0095 a0001c0003t0003g0100 |
2 | HG01261.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.517-1861A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623068 | |||||||
chr12:79623083 | C | T | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-1876G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623083 | |||||||
chr12:79623359 | C | T | 1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-2152G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623359 | |||||||
chr12:79623428 | G | A | 2 | a0001c0003t0003g0144 a0001c0003t0024g0148 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-2221C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623428 | |||||||
chr12:79623496 | T | C | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-2289A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623496 | |||||||
chr12:79623508 | G | GTTAC | 140 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(137): Show |
141 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.517-2302_517-2301i others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623508 | |||||||
chr12:79623559 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.517-2352A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623559 | |||||||
chr12:79623634 | CTT | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-2429_517-2428d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623634 | |||||||
chr12:79623643 | A | T | 1 | a0001c0001t0004g0034 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517-2436T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623643 | |||||||
chr12:79623903 | G | C | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-2696C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623903 | |||||||
chr12:79623946 | G | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-2739C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79623946 | |||||||
chr12:79624056 | G | A | 1 | a0001c0001t0004g0027 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.517-2849C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624056 | |||||||
chr12:79624197 | G | A | 1 | a0003c0004t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-2990C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624197 | |||||||
chr12:79624288 | C | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-3081G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624288 | |||||||
chr12:79624352 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-3145C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624352 | |||||||
chr12:79624635 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-3428T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624635 | |||||||
chr12:79624700 | G | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 |
3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-3493C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79624700 | |||||||
chr12:79625063 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-3856A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625063 | |||||||
chr12:79625133 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517-3926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625133 | |||||||
chr12:79625134 | C | A | 1 | a0002c0002t0001g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.517-3927G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625134 | |||||||
chr12:79625214 | A | G | 1 | a0001c0003t0013g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.517-4007T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625214 | |||||||
chr12:79625305 | C | T | 1 | a0002c0002t0001g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-4098G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625305 | |||||||
chr12:79625352 | A | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4145T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625352 | |||||||
chr12:79625559 | C | T | 1 | a0001c0001t0004g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517-4352G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625559 | |||||||
chr12:79625560 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0062 |
2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-4353C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625560 | |||||||
chr12:79625593 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4386C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625593 | |||||||
chr12:79625647 | T | C | 61 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(58): Show |
61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.517-4440A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625647 | |||||||
chr12:79625674 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-4467C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625674 | |||||||
chr12:79625675 | C | A | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-4468G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625675 | |||||||
chr12:79625681 | G | A | 1 | a0003c0004t0009g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-4474C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625681 | |||||||
chr12:79625721 | A | G | 1 | a0001c0001t0006g0022 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.517-4514T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625721 | |||||||
chr12:79625744 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4537G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625744 | |||||||
chr12:79625769 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.517-4562C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625769 | |||||||
chr12:79625777 | G | A | 2 | a0001c0003t0013g0040 a0001c0003t0013g0094 |
2 | HG02523.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.517-4570C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625777 | |||||||
chr12:79625848 | C | T | 4 | a0002c0002t0005g0245 a0002c0002t0005g0246 a0002c0002t0005g0247 others(1): Show |
4 | HG01109.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-4641G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625848 | |||||||
chr12:79625849 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-4642C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625849 | |||||||
chr12:79625870 | A | C | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-4663T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625870 | |||||||
chr12:79625874 | G | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0062 |
2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-4667C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625874 | |||||||
chr12:79625928 | T | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4721A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625928 | |||||||
chr12:79625931 | G | A | 1 | a0001c0003t0003g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-4724C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79625931 | |||||||
chr12:79626049 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.517-4842T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626049 | |||||||
chr12:79626089 | G | A | 15 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(12): Show |
15 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-4882C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626089 | |||||||
chr12:79626162 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-4955A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626162 | |||||||
chr12:79626162 | T | TAAAAAAA others(17): Show |
1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-4956_517-4955i others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626162 | |||||||
chr12:79626163 | T | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-4956A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | |||||||
chr12:79626163 | T | TA | 30 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0010 others(27): Show |
30 | HG00423.hp2 HG01099.hp2 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.517-4957dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | |||||||
chr12:79626163 | T | TAAAAAAA others(9): Show |
2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-4972_517-4957d others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | |||||||
chr12:79626163 | TA | T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(58): Show |
61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.517-4957delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | |||||||
chr12:79626163 | TAAAAAAA | T | 82 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(79): Show |
82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.517-4963_517-4957d others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626163 | |||||||
chr12:79626220 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5013T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626220 | |||||||
chr12:79626266 | T | C | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-5059A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626266 | |||||||
chr12:79626420 | C | T | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-5213G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626420 | |||||||
chr12:79626554 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.517-5347G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626554 | |||||||
chr12:79626579 | CT | C | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-5373delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626579 | |||||||
chr12:79626590 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.517-5383A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626590 | |||||||
chr12:79626789 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.517-5582A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626789 | |||||||
chr12:79626801 | C | T | 1 | a0001c0003t0028g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.517-5594G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626801 | |||||||
chr12:79626956 | G | A | 3 | a0001c0001t0002g0050 a0001c0001t0002g0092 a0001c0001t0002g0118 |
3 | HG00423.hp1 NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.517-5749C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626956 | |||||||
chr12:79626989 | T | C | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-5782A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626989 | |||||||
chr12:79626997 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5790A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79626997 | |||||||
chr12:79627052 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-5845C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627052 | |||||||
chr12:79627059 | T | C | 1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-5852A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627059 | |||||||
chr12:79627102 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-5895G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627102 | |||||||
chr12:79627150 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-5943G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627150 | |||||||
chr12:79627187 | C | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-5980G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627187 | |||||||
chr12:79627254 | G | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-6047C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627254 | |||||||
chr12:79627275 | C | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-6068G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627275 | |||||||
chr12:79627276 | G | A | 2 | a0001c0001t0004g0002 a0001c0001t0004g0003 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.517-6069C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627276 | |||||||
chr12:79627386 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-6179G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627386 | |||||||
chr12:79627417 | G | A | 1 | a0006c0008t0003g0097 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517-6210C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627417 | |||||||
chr12:79627486 | A | G | 2 | a0002c0002t0001g0225 a0002c0002t0012g0220 |
2 | NA18946.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.517-6279T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627486 | |||||||
chr12:79627501 | C | G | 1 | a0001c0001t0004g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-6294G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627501 | |||||||
chr12:79627899 | C | T | 2 | a0001c0003t0003g0149 a0001c0003t0023g0147 |
2 | NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.517-6692G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627899 | |||||||
chr12:79627978 | C | A | 1 | a0002c0002t0012g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.517-6771G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79627978 | |||||||
chr12:79628053 | A | G | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-6846T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628053 | |||||||
chr12:79628176 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-6969A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628176 | |||||||
chr12:79628190 | C | G | 1 | a0002c0002t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517-6983G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628190 | |||||||
chr12:79628259 | C | T | 1 | a0002c0002t0005g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.517-7052G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628259 | |||||||
chr12:79628662 | T | TA | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-7456dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628662 | |||||||
chr12:79628677 | C | T | 1 | a0001c0003t0008g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.517-7470G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628677 | |||||||
chr12:79628735 | G | A | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-7528C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79628735 | |||||||
chr12:79629001 | G | A | 1 | a0001c0001t0029g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517-7794C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629001 | |||||||
chr12:79629035 | C | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-7828G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629035 | |||||||
chr12:79629330 | G | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-8123C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629330 | |||||||
chr12:79629344 | T | A | 2 | a0002c0002t0005g0245 a0002c0002t0005g0247 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.517-8137A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629344 | |||||||
chr12:79629449 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.517-8242A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629449 | |||||||
chr12:79629734 | G | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-8527C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629734 | |||||||
chr12:79629943 | T | C | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-8736A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629943 | |||||||
chr12:79629959 | C | T | 1 | a0002c0002t0001g0198 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-8752G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79629959 | |||||||
chr12:79630074 | TA | T | 3 | a0001c0001t0004g0012 a0001c0001t0004g0034 a0001c0001t0004g0123 |
3 | HG01099.hp2 HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.517-8868delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630074 | |||||||
chr12:79630240 | A | G | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-9033T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630240 | |||||||
chr12:79630315 | A | T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(58): Show |
61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.517-9108T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630315 | |||||||
chr12:79630315 | ATT | A | 97 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(94): Show |
97 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.517-9110_517-9109d others(4): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630315 | |||||||
chr12:79630317 | T | A | 1 | a0003c0004t0001g0008 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.517-9110A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630317 | |||||||
chr12:79630368 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-9161G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630368 | |||||||
chr12:79630454 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-9247A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630454 | |||||||
chr12:79630634 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-9427A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630634 | |||||||
chr12:79630660 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-9453G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630660 | |||||||
chr12:79630858 | CA | C | 30 | a0001c0001t0002g0064 a0001c0003t0003g0081 a0002c0002t0001g0169 others(27): Show |
30 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.517-9652delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79630858 | |||||||
chr12:79631005 | T | A | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-9798A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631005 | |||||||
chr12:79631021 | A | T | 7 | a0002c0002t0001g0192 a0002c0002t0001g0198 a0002c0002t0001g0199 others(4): Show |
7 | HG00673.hp2 NA18945.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-9814T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631021 | |||||||
chr12:79631291 | G | A | 137 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(134): Show |
138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-10084C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631291 | |||||||
chr12:79631434 | A | C | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.517-10227T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631434 | |||||||
chr12:79631646 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517-10439C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631646 | |||||||
chr12:79631740 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517-10533T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631740 | |||||||
chr12:79631742 | T | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-10535A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631742 | |||||||
chr12:79631931 | G | A | 1 | a0006c0008t0003g0097 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.517-10724C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79631931 | |||||||
chr12:79632013 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-10806T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632013 | |||||||
chr12:79632089 | T | C | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-10882A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632089 | |||||||
chr12:79632132 | C | CA | 9 | a0001c0001t0002g0061 a0001c0001t0002g0067 a0001c0001t0002g0090 others(6): Show |
9 | HG00423.hp2 HG02074.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-10926dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | |||||||
chr12:79632132 | C | CAAAAAAA others(6): Show |
1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-10938_517-1092 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | |||||||
chr12:79632132 | C | CAAAAAAA others(7): Show |
2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-10939_517-1092 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | |||||||
chr12:79632132 | CA | C | 86 | a0001c0001t0004g0027 a0002c0002t0001g0168 a0002c0002t0001g0169 others(83): Show |
86 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.517-10926delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632132 | |||||||
chr12:79632151 | A | G | 7 | a0001c0001t0002g0063 a0001c0001t0002g0069 a0001c0001t0002g0071 others(4): Show |
7 | HG02040.hp1 NA18941.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-10944T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632151 | |||||||
chr12:79632174 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-10967T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632174 | |||||||
chr12:79632179 | A | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-10972T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632179 | |||||||
chr12:79632257 | A | ACAAAT | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11051_517-1105 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632257 | |||||||
chr12:79632288 | A | AATATATA others(7): Show |
3 | a0001c0001t0004g0020 a0001c0001t0006g0015 a0001c0001t0006g0033 |
3 | HG01109.hp2 HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.517-11095_517-1108 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(19): Show |
A | 1 | a0002c0002t0001g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.517-11107_517-1108 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(21): Show |
A | 1 | a0003c0004t0007g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.517-11109_517-1108 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(23): Show |
A | 1 | a0003c0004t0007g0167 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-11111_517-1108 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(31): Show |
A | 5 | a0002c0002t0001g0174 a0003c0004t0009g0156 a0003c0004t0009g0157 others(2): Show |
5 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-11119_517-1108 others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(33): Show |
A | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11121_517-1108 others(44): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(35): Show |
A | 1 | a0002c0002t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.517-11123_517-1108 others(46): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632288 | AATATATA others(37): Show |
A | 5 | a0002c0002t0005g0181 a0003c0004t0022g0165 a0004c0006t0011g0238 others(2): Show |
5 | HG00639.hp2 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-11125_517-1108 others(48): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632288 | |||||||
chr12:79632290 | TATATACA others(15): Show |
T | 3 | a0002c0002t0001g0169 a0002c0002t0001g0171 a0002c0002t0001g0252 |
3 | HG02572.hp1 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.517-11105_517-1108 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632290 | |||||||
chr12:79632292 | T | A | 1 | a0002c0002t0001g0211 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.517-11085A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | |||||||
chr12:79632292 | TATACATA others(9): Show |
T | 11 | a0001c0001t0002g0089 a0002c0002t0001g0172 a0002c0002t0001g0173 others(8): Show |
11 | HG01261.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-11101_517-1108 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | |||||||
chr12:79632292 | TATACATA others(13): Show |
T | 2 | a0002c0002t0001g0190 a0002c0002t0017g0183 |
2 | HG02027.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.517-11105_517-1108 others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632292 | |||||||
chr12:79632294 | TACATATA others(7): Show |
T | 10 | a0002c0002t0001g0177 a0002c0002t0001g0187 a0002c0002t0001g0201 others(7): Show |
10 | HG00621.hp2 HG01891.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-11101_517-1108 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632294 | |||||||
chr12:79632294 | TACATATA others(11): Show |
T | 11 | a0002c0002t0001g0170 a0002c0002t0001g0184 a0002c0002t0001g0186 others(8): Show |
11 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-11105_517-1108 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632294 | |||||||
chr12:79632296 | C | CAT | 24 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(21): Show |
25 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.517-11091_517-1109 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | C | CATATATA others(11): Show |
3 | a0001c0001t0004g0014 a0001c0001t0004g0017 a0001c0001t0004g0019 |
3 | HG02615.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.517-11090_517-1108 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | C | CATATATA others(25): Show |
3 | a0001c0001t0004g0030 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG02080.hp1 HG02683.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.517-11090_517-1108 others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | C | CATATATA others(55): Show |
1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-11090_517-1108 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | C | T | 46 | a0002c0002t0001g0168 a0002c0002t0001g0175 a0002c0002t0001g0179 others(43): Show |
46 | HG00544.hp2 HG00673.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.517-11089G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(15): Show |
C | 1 | a0001c0003t0003g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.517-11111_517-1109 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(17): Show |
C | 1 | a0001c0003t0003g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-11113_517-1109 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(19): Show |
C | 2 | a0001c0001t0003g0039 a0001c0003t0003g0084 |
2 | HG02071.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.517-11115_517-1109 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(21): Show |
C | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.517-11117_517-1109 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(25): Show |
C | 2 | a0001c0001t0002g0048 a0001c0001t0016g0013 |
2 | HG02055.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.517-11121_517-1109 others(36): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632296 | CATATATA others(39): Show |
C | 2 | a0001c0001t0002g0063 a0001c0001t0002g0071 |
2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.517-11135_517-1109 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632296 | |||||||
chr12:79632298 | TATATATA others(7): Show |
T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(13): Show |
16 | HG00741.hp1 HG01243.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632298 | |||||||
chr12:79632300 | TATATATA others(5): Show |
T | 43 | a0001c0001t0002g0054 a0001c0001t0002g0057 a0001c0001t0002g0059 others(40): Show |
43 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632300 | |||||||
chr12:79632302 | TATATACA others(3): Show |
T | 13 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0003t0003g0077 others(10): Show |
13 | HG00621.hp1 HG01069.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632302 | |||||||
chr12:79632302 | TATATACA others(38): Show |
T | 1 | a0002c0002t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.517-11140_517-1109 others(49): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632302 | |||||||
chr12:79632303 | ATATACAT others(52): Show |
A | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-11155_517-1109 others(63): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632303 | |||||||
chr12:79632304 | TATACATA others(1): Show |
T | 8 | a0001c0001t0002g0056 a0001c0001t0002g0120 a0001c0003t0027g0134 others(5): Show |
8 | HG02145.hp2 HG02886.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-11105_517-1109 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632304 | |||||||
chr12:79632304 | TATACATA others(40): Show |
T | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-11144_517-1109 others(51): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632304 | |||||||
chr12:79632306 | TACATAC | T | 9 | a0001c0001t0002g0073 a0001c0001t0002g0079 a0001c0003t0003g0096 others(6): Show |
9 | HG01069.hp1 HG01192.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-11105_517-1110 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632306 | |||||||
chr12:79632307 | ACATACAT others(55): Show |
A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-11162_517-1110 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632307 | |||||||
chr12:79632308 | C | T | 63 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0068 others(60): Show |
63 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.517-11101G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632308 | |||||||
chr12:79632310 | T | C | 4 | a0001c0001t0004g0010 a0001c0001t0004g0027 a0001c0001t0004g0029 others(1): Show |
4 | HG02257.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11103A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632310 | |||||||
chr12:79632312 | C | CATATATA others(5): Show |
2 | a0001c0001t0002g0133 a0001c0003t0003g0074 |
2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.517-11117_517-1110 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | |||||||
chr12:79632312 | C | T | 62 | a0001c0001t0002g0076 a0001c0001t0004g0001 a0001c0001t0004g0002 others(59): Show |
63 | HG00423.hp2 HG00621.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.517-11105G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | |||||||
chr12:79632312 | CAT | C | 5 | a0001c0001t0002g0068 a0001c0003t0003g0099 a0001c0003t0003g0145 others(2): Show |
5 | HG00741.hp2 HG02056.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11107_517-1110 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | |||||||
chr12:79632312 | CATAT | C | 4 | a0001c0003t0003g0101 a0001c0003t0003g0102 a0001c0003t0003g0144 others(1): Show |
4 | HG01169.hp1 HG01891.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11109_517-1110 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632312 | |||||||
chr12:79632316 | T | TATATATA others(1): Show |
3 | a0001c0001t0004g0016 a0001c0001t0004g0031 a0001c0001t0006g0025 |
3 | HG03516.hp1 HG03654.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.517-11110_517-1110 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632316 | |||||||
chr12:79632318 | T | C | 5 | a0001c0001t0002g0073 a0001c0001t0002g0079 a0001c0003t0003g0096 others(2): Show |
5 | HG01069.hp1 HG01192.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11111A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632318 | |||||||
chr12:79632318 | T | TATATACA others(15): Show |
1 | a0001c0001t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.517-11112_517-1111 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632318 | |||||||
chr12:79632320 | T | C | 3 | a0001c0001t0002g0056 a0001c0001t0002g0120 a0001c0003t0027g0134 |
3 | HG03831.hp2 NA19003.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.517-11113A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632320 | |||||||
chr12:79632322 | T | C | 8 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0003t0003g0077 others(5): Show |
8 | HG00621.hp1 HG01069.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-11115A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632322 | |||||||
chr12:79632324 | T | C | 46 | a0001c0001t0002g0054 a0001c0001t0002g0057 a0001c0001t0002g0059 others(43): Show |
46 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.517-11117A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632324 | |||||||
chr12:79632324 | T | TATATATA others(13): Show |
1 | a0001c0001t0002g0152 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.517-11118_517-1111 others(24): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632324 | |||||||
chr12:79632326 | T | C | 19 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(16): Show |
19 | HG00741.hp1 HG01243.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-11119A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632326 | |||||||
chr12:79632326 | T | TATATATA others(11): Show |
3 | a0001c0001t0002g0106 a0001c0001t0002g0110 a0001c0001t0002g0115 |
3 | NA18987.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-11120_517-1111 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632326 | |||||||
chr12:79632328 | T | C | 3 | a0001c0001t0002g0089 a0001c0001t0002g0116 a0001c0001t0002g0117 |
3 | HG01168.hp1 HG01169.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.517-11121A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632328 | |||||||
chr12:79632330 | T | G | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11123A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632330 | |||||||
chr12:79632332 | T | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11125A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632332 | |||||||
chr12:79632334 | T | C | 2 | a0001c0001t0016g0013 a0001c0003t0003g0085 |
2 | HG02055.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.517-11127A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632334 | |||||||
chr12:79632338 | T | C | 12 | a0001c0001t0003g0039 a0001c0001t0004g0012 a0001c0001t0004g0030 others(9): Show |
12 | HG01099.hp2 HG02040.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-11131A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632338 | |||||||
chr12:79632339 | A | T | 1 | a0002c0002t0001g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11132T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632339 | |||||||
chr12:79632340 | T | C | 3 | a0001c0001t0002g0068 a0001c0001t0003g0037 a0001c0001t0003g0038 |
3 | HG02572.hp2 HG03041.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.517-11133A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632340 | |||||||
chr12:79632341 | A | T | 1 | a0002c0002t0001g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11134T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632341 | |||||||
chr12:79632341 | ATATATAT others(15): Show |
A | 5 | a0001c0003t0002g0154 a0001c0003t0003g0130 a0001c0003t0003g0131 others(2): Show |
5 | HG00544.hp1 NA18967.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11156_517-1113 others(26): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632341 | |||||||
chr12:79632343 | A | T | 1 | a0002c0002t0001g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11136T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632343 | |||||||
chr12:79632344 | T | C | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-11137A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632344 | |||||||
chr12:79632345 | A | T | 1 | a0002c0002t0001g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-11138T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632345 | |||||||
chr12:79632346 | T | TATATATA others(4): Show |
2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-11140_517-1113 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632346 | |||||||
chr12:79632346 | TA | T | 8 | a0002c0002t0001g0175 a0002c0002t0001g0187 a0002c0002t0001g0190 others(5): Show |
8 | HG02027.hp2 HG02258.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-11140delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632346 | |||||||
chr12:79632347 | A | T | 2 | a0002c0002t0001g0179 a0002c0002t0001g0191 |
2 | HG02559.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.517-11140T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632347 | |||||||
chr12:79632348 | T | C | 1 | a0001c0003t0003g0146 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.517-11141A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | |||||||
chr12:79632348 | TA | T | 5 | a0002c0002t0001g0194 a0002c0002t0001g0207 a0002c0002t0001g0208 others(2): Show |
5 | HG01975.hp2 HG02071.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11142delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | |||||||
chr12:79632348 | TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0113 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.517-11154_517-1114 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632348 | |||||||
chr12:79632349 | A | T | 23 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0175 others(20): Show |
23 | HG01256.hp1 HG01258.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.517-11142T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | |||||||
chr12:79632349 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0091 a0001c0001t0003g0108 |
2 | NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.517-11155_517-1114 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | |||||||
chr12:79632349 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0107 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.517-11156_517-1114 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632349 | |||||||
chr12:79632350 | TA | T | 3 | a0002c0002t0001g0170 a0002c0002t0001g0199 a0002c0002t0001g0222 |
3 | HG00621.hp2 HG01192.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.517-11144delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632350 | |||||||
chr12:79632350 | TATATATA others(4): Show |
T | 2 | a0001c0003t0003g0098 a0001c0003t0008g0138 |
2 | HG01928.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.517-11154_517-1114 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632350 | |||||||
chr12:79632351 | A | T | 46 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0172 others(43): Show |
46 | HG00544.hp2 HG00673.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.517-11144T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632351 | |||||||
chr12:79632351 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0050 a0001c0001t0029g0119 |
2 | HG00423.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.517-11156_517-1114 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632351 | |||||||
chr12:79632352 | TATATATA others(2): Show |
T | 4 | a0001c0003t0008g0135 a0001c0003t0008g0136 a0001c0003t0008g0137 others(1): Show |
4 | NA18946.hp1 NA18966.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11154_517-1114 others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632352 | |||||||
chr12:79632353 | A | G | 1 | a0001c0001t0004g0014 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.517-11146T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | |||||||
chr12:79632353 | A | T | 75 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(72): Show |
75 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.517-11146T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | |||||||
chr12:79632353 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0051 a0001c0001t0002g0118 a0001c0003t0003g0045 |
3 | HG01952.hp2 HG02080.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.517-11156_517-1114 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632353 | |||||||
chr12:79632355 | A | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-11148T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632355 | |||||||
chr12:79632357 | A | T | 85 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(82): Show |
85 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.517-11150T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632357 | |||||||
chr12:79632359 | A | T | 87 | a0001c0001t0004g0018 a0002c0002t0001g0168 a0002c0002t0001g0169 others(84): Show |
87 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.517-11152T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632359 | |||||||
chr12:79632361 | A | AT | 7 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0026 others(4): Show |
7 | HG01993.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-11155dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632361 | |||||||
chr12:79632361 | A | T | 119 | a0001c0001t0002g0042 a0001c0001t0002g0089 a0001c0001t0002g0122 others(116): Show |
119 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.517-11154T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632361 | |||||||
chr12:79632363 | T | A | 4 | a0001c0003t0003g0095 a0004c0006t0011g0238 a0004c0006t0011g0239 others(1): Show |
4 | HG01261.hp2 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-11156A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632363 | |||||||
chr12:79632377 | A | T | 1 | a0001c0003t0003g0132 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.517-11170T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632377 | |||||||
chr12:79632428 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-11221C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632428 | |||||||
chr12:79632545 | A | C | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-11338T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632545 | |||||||
chr12:79632772 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517-11565G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632772 | |||||||
chr12:79632773 | C | G | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-11566G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632773 | |||||||
chr12:79632855 | C | T | 2 | a0001c0001t0004g0002 a0001c0001t0004g0003 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.517-11648G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632855 | |||||||
chr12:79632882 | C | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11675G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79632882 | |||||||
chr12:79633126 | A | AAAAC | 4 | a0002c0002t0001g0224 a0004c0006t0011g0238 a0004c0006t0011g0239 others(1): Show |
4 | HG02258.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-11923_517-1192 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633126 | |||||||
chr12:79633187 | T | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-11980A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633187 | |||||||
chr12:79633260 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12053A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633260 | |||||||
chr12:79633514 | G | GT | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-12308dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633514 | |||||||
chr12:79633514 | G | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12307C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633514 | |||||||
chr12:79633526 | T | C | 1 | a0001c0003t0003g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-12319A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633526 | |||||||
chr12:79633716 | C | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-12509G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633716 | |||||||
chr12:79633955 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-12748G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633955 | |||||||
chr12:79633973 | A | G | 1 | a0001c0001t0006g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517-12766T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633973 | |||||||
chr12:79633974 | G | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 |
3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-12767C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79633974 | |||||||
chr12:79634061 | G | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-12854C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634061 | |||||||
chr12:79634664 | A | AAGAAAC | 137 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(134): Show |
138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-13458_517-1345 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634664 | |||||||
chr12:79634958 | C | T | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-13751G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634958 | |||||||
chr12:79634966 | C | A | 1 | a0001c0003t0003g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.517-13759G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79634966 | |||||||
chr12:79635032 | C | T | 1 | a0002c0002t0020g0193 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.517-13825G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635032 | |||||||
chr12:79635150 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-13943T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635150 | |||||||
chr12:79635464 | T | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-14257A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635464 | |||||||
chr12:79635643 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-14436C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635643 | |||||||
chr12:79635736 | T | G | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-14529A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79635736 | |||||||
chr12:79636338 | C | CAT | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-15132_517-1513 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636338 | |||||||
chr12:79636656 | C | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-15449G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636656 | |||||||
chr12:79636666 | T | C | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-15459A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636666 | |||||||
chr12:79636699 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0062 |
2 | HG02027.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.517-15492G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636699 | |||||||
chr12:79636927 | T | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-15720A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636927 | |||||||
chr12:79636939 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-15732A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79636939 | |||||||
chr12:79637191 | G | C | 4 | a0002c0002t0001g0171 a0002c0002t0001g0210 a0002c0002t0001g0211 others(1): Show |
4 | HG03139.hp1 NA18906.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-15984C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637191 | |||||||
chr12:79637446 | C | T | 1 | a0001c0003t0014g0161 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517-16239G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637446 | |||||||
chr12:79637489 | T | TAAGCCAA others(9): Show |
1 | a0002c0002t0001g0217 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-16298_517-1628 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637489 | |||||||
chr12:79637541 | T | TAAAAAAA others(317): Show |
2 | a0003c0004t0009g0158 a0003c0004t0009g0159 |
2 | HG01074.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.517-16335_517-1633 others(328): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | |||||||
chr12:79637541 | T | TAAAAAAA others(319): Show |
1 | a0003c0004t0009g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517-16335_517-1633 others(330): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | |||||||
chr12:79637541 | T | TAAAAAAA others(320): Show |
1 | a0003c0004t0009g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.517-16335_517-1633 others(331): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | |||||||
chr12:79637541 | TA | T | 92 | a0001c0001t0004g0026 a0002c0002t0001g0168 a0002c0002t0001g0169 others(89): Show |
92 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.517-16335delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637541 | |||||||
chr12:79637649 | A | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-16442T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637649 | |||||||
chr12:79637656 | C | T | 1 | a0004c0006t0011g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.517-16449G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637656 | |||||||
chr12:79637977 | A | G | 1 | a0001c0003t0003g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-16770T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79637977 | |||||||
chr12:79638138 | C | CA | 14 | a0002c0002t0005g0181 a0002c0002t0005g0182 a0002c0002t0005g0232 others(11): Show |
14 | HG00639.hp2 HG01109.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-16932dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638138 | |||||||
chr12:79638288 | T | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0112 |
2 | HG01928.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.517-17081A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638288 | |||||||
chr12:79638466 | T | C | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-17259A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638466 | |||||||
chr12:79638757 | C | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17550G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638757 | |||||||
chr12:79638790 | G | GGT | 69 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0043 others(66): Show |
69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.517-17585_517-1758 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | |||||||
chr12:79638790 | G | GGTGT | 3 | a0001c0001t0002g0051 a0001c0001t0002g0079 a0001c0003t0003g0085 |
3 | HG01192.hp2 HG02080.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.517-17587_517-1758 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | |||||||
chr12:79638790 | G | GT | 7 | a0001c0001t0002g0073 a0001c0001t0004g0035 a0001c0003t0002g0154 others(4): Show |
7 | HG00423.hp2 HG01069.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-17584_517-1758 others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | |||||||
chr12:79638790 | GGT | G | 88 | a0001c0003t0003g0045 a0001c0003t0003g0082 a0002c0002t0001g0168 others(85): Show |
88 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.517-17585_517-1758 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | |||||||
chr12:79638790 | GGTGTGTG others(3): Show |
G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17593_517-1758 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638790 | |||||||
chr12:79638794 | T | G | 18 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0180 others(15): Show |
18 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.517-17587A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638794 | |||||||
chr12:79638810 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-17603A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638810 | |||||||
chr12:79638863 | C | CAT | 6 | a0001c0001t0002g0091 a0001c0003t0003g0081 a0001c0003t0008g0150 others(3): Show |
6 | HG00673.hp2 HG02602.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-17658_517-1765 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATAT | 10 | a0001c0001t0002g0054 a0001c0001t0002g0080 a0001c0001t0002g0104 others(7): Show |
10 | HG00544.hp2 HG00639.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-17660_517-1765 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATAT | 5 | a0001c0001t0004g0035 a0001c0003t0002g0154 a0002c0002t0001g0187 others(2): Show |
5 | HG00423.hp2 HG01169.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17662_517-1765 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(1): Show |
12 | a0001c0001t0002g0070 a0001c0001t0002g0079 a0001c0001t0002g0116 others(9): Show |
12 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.517-17664_517-1765 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(3): Show |
10 | a0001c0001t0002g0041 a0001c0001t0002g0047 a0001c0001t0002g0048 others(7): Show |
10 | HG00438.hp1 HG01099.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-17666_517-1765 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(5): Show |
6 | a0001c0001t0002g0050 a0001c0001t0002g0069 a0001c0001t0002g0071 others(3): Show |
6 | HG00423.hp1 HG02040.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-17668_517-1765 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(7): Show |
4 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0122 others(1): Show |
4 | HG00741.hp1 HG01069.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17670_517-1765 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(9): Show |
1 | a0001c0001t0002g0061 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.517-17672_517-1765 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638863 | C | CATATATA others(17): Show |
1 | a0001c0001t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517-17680_517-1765 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638863 | |||||||
chr12:79638868 | ATATATAT others(34): Show |
A | 4 | a0002c0002t0001g0171 a0002c0002t0001g0210 a0002c0002t0001g0211 others(1): Show |
4 | HG03139.hp1 NA18906.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17702_517-1766 others(45): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638868 | |||||||
chr12:79638876 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0152 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.517-17670_517-1766 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638876 | |||||||
chr12:79638878 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0115 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.517-17672_517-1767 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638878 | |||||||
chr12:79638878 | ATATATAT others(31): Show |
A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-17709_517-1767 others(42): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638878 | |||||||
chr12:79638880 | ATATATAT others(17): Show |
A | 1 | a0003c0004t0009g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-17697_517-1767 others(28): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | |||||||
chr12:79638880 | ATATATAT others(18): Show |
A | 2 | a0003c0004t0009g0156 a0003c0004t0009g0159 |
2 | HG01074.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.517-17698_517-1767 others(29): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | |||||||
chr12:79638880 | ATATATAT others(19): Show |
A | 1 | a0003c0004t0009g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.517-17699_517-1767 others(30): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638880 | |||||||
chr12:79638890 | ATATATAT others(7): Show |
A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-17697_517-1768 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638890 | |||||||
chr12:79638892 | A | T | 1 | a0001c0003t0014g0161 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.517-17685T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638892 | |||||||
chr12:79638894 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0110 |
2 | NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-17687T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638894 | |||||||
chr12:79638894 | A | T | 2 | a0001c0001t0004g0023 a0001c0003t0014g0161 |
2 | HG02074.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.517-17687T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638894 | |||||||
chr12:79638896 | A | ATAT | 5 | a0001c0001t0004g0014 a0001c0001t0004g0016 a0001c0001t0004g0021 others(2): Show |
5 | HG01255.hp1 HG01981.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17690_517-1768 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(4): Show |
3 | a0001c0001t0002g0112 a0001c0001t0003g0053 a0001c0001t0026g0055 |
3 | HG01928.hp2 NA18941.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0092 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(8): Show |
1 | a0001c0003t0027g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(9): Show |
1 | a0001c0001t0004g0028 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(5): Show |
1 | a0001c0003t0031g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0064 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(5): Show |
1 | a0001c0001t0004g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0127 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(3): Show |
2 | a0001c0001t0010g0125 a0001c0003t0003g0084 |
2 | HG02071.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(5): Show |
1 | a0001c0001t0006g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(6): Show |
2 | a0001c0001t0010g0126 a0001c0001t0010g0128 |
2 | NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.517-17690_517-1768 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATATAT others(9): Show |
1 | a0001c0001t0004g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATTT | 5 | a0001c0001t0004g0010 a0001c0001t0006g0025 a0001c0003t0003g0074 others(2): Show |
5 | HG01074.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17690_517-1768 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATTTTT others(5): Show |
1 | a0001c0001t0004g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.517-17690_517-1768 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | ATATTTTT others(12): Show |
1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517-17690_517-1768 others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | A | T | 5 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0004g0023 others(2): Show |
5 | HG02074.hp2 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17689T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | AT | A | 11 | a0002c0002t0001g0180 a0002c0002t0001g0184 a0002c0002t0001g0192 others(8): Show |
11 | HG02622.hp1 HG03225.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-17690delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATT | A | 7 | a0001c0001t0002g0051 a0002c0002t0001g0179 a0002c0002t0001g0198 others(4): Show |
7 | HG02080.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATTT | A | 14 | a0002c0002t0001g0168 a0002c0002t0001g0191 a0002c0002t0001g0216 others(11): Show |
14 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-17692_517-1769 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATTTTT | A | 9 | a0001c0001t0004g0030 a0001c0001t0006g0022 a0002c0002t0001g0175 others(6): Show |
9 | HG01168.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-17694_517-1769 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATTTTTT | A | 5 | a0001c0001t0004g0032 a0002c0002t0001g0170 a0002c0002t0001g0231 others(2): Show |
5 | HG01192.hp1 HG02040.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-17695_517-1769 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATTTTTTT others(1): Show |
A | 5 | a0001c0001t0004g0001 a0002c0002t0001g0186 a0002c0002t0001g0227 others(2): Show |
5 | HG01258.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17697_517-1769 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638896 | ATTTTTTT others(5): Show |
A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17701_517-1769 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638896 | |||||||
chr12:79638897 | T | TA | 9 | a0001c0001t0002g0066 a0001c0001t0002g0072 a0001c0003t0024g0148 others(6): Show |
9 | HG01255.hp2 HG02071.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(5): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATA | 10 | a0001c0001t0004g0019 a0001c0003t0003g0077 a0002c0002t0001g0189 others(7): Show |
10 | HG00621.hp1 HG01975.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATA | 4 | a0001c0003t0003g0085 a0001c0003t0003g0088 a0002c0002t0001g0196 others(1): Show |
4 | HG02300.hp1 NA18969.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATATA | 9 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0067 others(6): Show |
9 | HG00621.hp2 HG01952.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATATA others(2): Show |
6 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0052 others(3): Show |
6 | HG01081.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(13): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATATA others(4): Show |
5 | a0001c0001t0002g0063 a0001c0001t0002g0090 a0001c0001t0002g0133 others(2): Show |
5 | HG00673.hp1 HG01069.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-17691_517-1769 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATATA others(10): Show |
2 | a0001c0001t0002g0106 a0001c0001t0002g0110 |
2 | NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.517-17691_517-1769 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638897 | T | TATATATA others(16): Show |
1 | a0001c0001t0002g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-17691_517-1769 others(27): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638897 | |||||||
chr12:79638898 | T | A | 34 | a0001c0001t0002g0041 a0001c0001t0002g0047 a0001c0001t0002g0054 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.517-17691A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638898 | |||||||
chr12:79638899 | T | A | 38 | a0001c0001t0002g0042 a0001c0001t0002g0052 a0001c0001t0002g0060 others(35): Show |
38 | HG00621.hp2 HG00673.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-17692A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638899 | |||||||
chr12:79638900 | T | A | 26 | a0001c0001t0002g0047 a0001c0001t0002g0054 a0001c0001t0002g0080 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.517-17693A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638900 | |||||||
chr12:79638901 | T | A | 39 | a0001c0001t0002g0072 a0001c0001t0002g0133 a0002c0002t0001g0168 others(36): Show |
39 | HG00621.hp2 HG00673.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.517-17694A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638901 | |||||||
chr12:79638901 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.517-17694A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638901 | |||||||
chr12:79638902 | T | A | 22 | a0001c0001t0002g0047 a0001c0001t0004g0124 a0001c0003t0023g0147 others(19): Show |
22 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.517-17695A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638902 | |||||||
chr12:79638903 | T | A | 33 | a0001c0001t0004g0030 a0002c0002t0001g0168 a0002c0002t0001g0175 others(30): Show |
33 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.517-17696A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638903 | |||||||
chr12:79638904 | T | A | 23 | a0001c0001t0002g0047 a0001c0001t0004g0032 a0001c0001t0004g0124 others(20): Show |
23 | HG00544.hp2 HG00639.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.517-17697A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638904 | |||||||
chr12:79638905 | T | A | 28 | a0001c0001t0004g0001 a0002c0002t0001g0175 a0002c0002t0001g0177 others(25): Show |
28 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.517-17698A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638905 | |||||||
chr12:79638906 | T | A | 21 | a0001c0001t0002g0047 a0001c0001t0004g0001 a0002c0002t0001g0169 others(18): Show |
21 | HG01192.hp1 HG01258.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.517-17699A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638906 | |||||||
chr12:79638907 | T | A | 19 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0177 others(16): Show |
19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.517-17700A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638907 | |||||||
chr12:79638908 | T | A | 12 | a0001c0001t0002g0047 a0002c0002t0001g0169 a0002c0002t0001g0170 others(9): Show |
12 | HG01192.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.517-17701A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638908 | |||||||
chr12:79638909 | T | A | 11 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0180 others(8): Show |
11 | HG01261.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-17702A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638909 | |||||||
chr12:79638910 | T | A | 9 | a0001c0001t0002g0047 a0002c0002t0001g0169 a0002c0002t0001g0179 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-17703A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638910 | |||||||
chr12:79638911 | T | A | 2 | a0002c0002t0001g0174 a0002c0002t0018g0244 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.517-17704A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638911 | |||||||
chr12:79638912 | T | A | 3 | a0002c0002t0001g0218 a0002c0002t0001g0229 a0002c0002t0001g0231 |
3 | HG02145.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.517-17705A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638912 | |||||||
chr12:79638914 | T | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17707A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638914 | |||||||
chr12:79638916 | T | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17709A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638916 | |||||||
chr12:79638918 | T | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-17711A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79638918 | |||||||
chr12:79639027 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.517-17820G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639027 | |||||||
chr12:79639049 | G | A | 1 | a0001c0001t0025g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-17842C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639049 | |||||||
chr12:79639078 | A | G | 1 | a0002c0002t0001g0189 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.517-17871T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639078 | |||||||
chr12:79639133 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-17926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639133 | |||||||
chr12:79639177 | C | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.517-17970G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639177 | |||||||
chr12:79639322 | C | A | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-18115G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639322 | |||||||
chr12:79639536 | A | C | 1 | a0002c0002t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.517-18329T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639536 | |||||||
chr12:79639567 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-18360A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639567 | |||||||
chr12:79639694 | G | A | 4 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0029 others(1): Show |
4 | NA18945.hp2 NA18966.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-18487C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639694 | |||||||
chr12:79639811 | A | ATTCCTT | 75 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0171 others(72): Show |
75 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.517-18610_517-1860 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | |||||||
chr12:79639811 | A | ATTCCTTT others(5): Show |
1 | a0002c0002t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-18616_517-1860 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | |||||||
chr12:79639811 | ATTCCTT | A | 7 | a0001c0001t0004g0034 a0001c0001t0004g0123 a0003c0004t0007g0166 others(4): Show |
7 | HG01099.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-18610_517-1860 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639811 | |||||||
chr12:79639831 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-18624A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639831 | |||||||
chr12:79639831 | T | TCCTTTTC others(47): Show |
1 | a0002c0002t0001g0241 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.517-18625_517-1862 others(58): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639831 | |||||||
chr12:79639832 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(56): Show |
59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.517-18625G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639832 | |||||||
chr12:79639833 | C | CATTCCTA others(23): Show |
1 | a0002c0002t0005g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-18656_517-1862 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | C | CATTCCTA others(41): Show |
1 | a0002c0002t0018g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.517-18674_517-1862 others(52): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | C | CTTTCCTA others(53): Show |
1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-18627_517-1862 others(64): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | C | T | 60 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(57): Show |
60 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.517-18626G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | CATTCCT | C | 42 | a0001c0003t0002g0154 a0001c0003t0003g0006 a0001c0003t0003g0045 others(39): Show |
42 | HG00544.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.517-18632_517-1862 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | CATTCCTA others(5): Show |
C | 7 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-18638_517-1862 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639833 | CATTCCTA others(11): Show |
C | 42 | a0001c0001t0002g0115 a0001c0001t0004g0001 a0001c0001t0004g0002 others(39): Show |
43 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.517-18644_517-1862 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639833 | |||||||
chr12:79639834 | A | T | 1 | a0002c0002t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.517-18627T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639834 | |||||||
chr12:79639837 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.517-18630G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639837 | |||||||
chr12:79639838 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0003g0053 |
2 | HG01928.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.517-18631G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639838 | |||||||
chr12:79639839 | T | C | 9 | a0002c0002t0001g0206 a0002c0002t0001g0214 a0002c0002t0001g0230 others(6): Show |
9 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-18632A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639839 | |||||||
chr12:79639840 | A | T | 1 | a0002c0002t0001g0236 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.517-18633T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639840 | |||||||
chr12:79639845 | T | C | 9 | a0002c0002t0001g0206 a0002c0002t0001g0224 a0002c0002t0001g0230 others(6): Show |
9 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-18638A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639845 | |||||||
chr12:79639851 | T | C | 10 | a0002c0002t0001g0206 a0002c0002t0001g0217 a0002c0002t0001g0224 others(7): Show |
10 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-18644A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639851 | |||||||
chr12:79639857 | T | C | 8 | a0002c0002t0001g0224 a0002c0002t0001g0230 a0002c0002t0001g0241 others(5): Show |
8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18650A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639857 | |||||||
chr12:79639863 | T | C | 8 | a0002c0002t0001g0224 a0002c0002t0001g0230 a0002c0002t0001g0241 others(5): Show |
8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18656A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639863 | |||||||
chr12:79639863 | TATTCCTA others(21): Show |
T | 6 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-18684_517-1865 others(32): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639863 | |||||||
chr12:79639869 | T | C | 8 | a0002c0002t0001g0224 a0002c0002t0001g0230 a0002c0002t0001g0241 others(5): Show |
8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18662A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639869 | |||||||
chr12:79639869 | TATTCCTA others(10): Show |
T | 3 | a0001c0001t0002g0080 a0005c0007t0033g0255 a0005c0007t0034g0254 |
3 | HG02145.hp1 HG02976.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.517-18679_517-1866 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639869 | |||||||
chr12:79639874 | CT | C | 35 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(32): Show |
35 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.517-18668delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639874 | |||||||
chr12:79639874 | CTATTCCT | C | 5 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 others(2): Show |
5 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-18674_517-1866 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639874 | |||||||
chr12:79639875 | T | C | 8 | a0002c0002t0001g0197 a0002c0002t0001g0224 a0002c0002t0001g0230 others(5): Show |
8 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18668A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639875 | |||||||
chr12:79639875 | TATTCCTA others(4): Show |
T | 1 | a0001c0003t0008g0135 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.517-18679_517-1866 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639875 | |||||||
chr12:79639879 | C | CCATT | 8 | a0002c0002t0001g0174 a0002c0002t0001g0197 a0002c0002t0001g0203 others(5): Show |
8 | HG02895.hp1 HG03516.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-18673_517-1867 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCATTCCA others(212): Show |
1 | a0002c0002t0001g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(223): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCATTCCA others(262): Show |
1 | a0002c0002t0001g0217 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(273): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(57): Show |
1 | a0002c0002t0005g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(68): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(64): Show |
2 | a0002c0002t0001g0230 a0002c0002t0019g0178 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-18673_517-1867 others(75): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(82): Show |
1 | a0002c0002t0001g0224 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(93): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(51): Show |
1 | a0002c0002t0005g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.517-18673_517-1867 others(62): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(45): Show |
1 | a0002c0002t0005g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-18673_517-1867 others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639879 | C | CCCATTCC others(39): Show |
1 | a0002c0002t0005g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-18673_517-1867 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639879 | |||||||
chr12:79639880 | CT | C | 35 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(32): Show |
35 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.517-18674delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639880 | |||||||
chr12:79639881 | T | C | 17 | a0002c0002t0001g0174 a0002c0002t0001g0197 a0002c0002t0001g0203 others(14): Show |
17 | HG01261.hp1 HG02630.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.517-18674A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCAT others(3): Show |
4 | a0002c0002t0001g0184 a0002c0002t0001g0186 a0002c0002t0001g0236 others(1): Show |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-18684_517-1867 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(24): Show |
1 | a0002c0002t0001g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(35): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(22): Show |
1 | a0002c0002t0005g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(33): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(32): Show |
1 | a0002c0002t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(43): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(23): Show |
1 | a0002c0002t0015g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(34): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(28): Show |
1 | a0002c0002t0001g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(39): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(33): Show |
1 | a0002c0002t0017g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(44): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(39): Show |
1 | a0002c0002t0001g0175 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(50): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(45): Show |
1 | a0002c0002t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(56): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(55): Show |
1 | a0002c0002t0001g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(66): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(63): Show |
1 | a0002c0002t0005g0181 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(74): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(70): Show |
2 | a0002c0002t0001g0231 a0002c0002t0005g0232 |
2 | HG02055.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.517-18675_517-1867 others(81): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(75): Show |
1 | a0002c0002t0005g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(86): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(85): Show |
1 | a0002c0002t0005g0250 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.517-18675_517-1867 others(96): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(86): Show |
1 | a0002c0002t0005g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(97): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(97): Show |
1 | a0002c0002t0001g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(108): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | T | TATTCCTA others(108): Show |
1 | a0002c0002t0005g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517-18675_517-1867 others(119): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | TATTCC | T | 62 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(59): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-18679_517-1867 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639881 | TATTCCAT others(3): Show |
T | 1 | a0001c0001t0025g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-18684_517-1867 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639881 | |||||||
chr12:79639911 | C | CATTCCAT others(8): Show |
1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-18705_517-1870 others(19): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639911 | |||||||
chr12:79639911 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-18704G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639911 | |||||||
chr12:79639916 | T | C | 5 | a0001c0003t0003g0093 a0002c0002t0001g0230 a0002c0002t0005g0181 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-18709A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639916 | |||||||
chr12:79639975 | TCTAAGCG others(10): Show |
T | 1 | a0002c0002t0005g0246 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517-18785_517-1876 others(21): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639975 | |||||||
chr12:79639982 | G | A | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-18775C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79639982 | |||||||
chr12:79640022 | A | G | 2 | a0002c0002t0001g0216 a0002c0002t0001g0221 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.517-18815T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640022 | |||||||
chr12:79640183 | C | A | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-18976G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640183 | |||||||
chr12:79640191 | C | T | 1 | a0001c0003t0003g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-18984G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640191 | |||||||
chr12:79640434 | C | T | 1 | a0003c0004t0009g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-19227G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640434 | |||||||
chr12:79640565 | ACT | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-19360_517-1935 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640565 | |||||||
chr12:79640642 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-19435C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640642 | |||||||
chr12:79640703 | T | C | 3 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 |
3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-19496A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640703 | |||||||
chr12:79640738 | C | T | 4 | a0001c0001t0002g0057 a0001c0001t0002g0059 a0001c0001t0002g0060 others(1): Show |
4 | HG01081.hp1 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-19531G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640738 | |||||||
chr12:79640972 | T | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-19765A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640972 | |||||||
chr12:79640974 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-19767C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79640974 | |||||||
chr12:79641257 | G | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-20050C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641257 | |||||||
chr12:79641289 | A | T | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-20082T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641289 | |||||||
chr12:79641582 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-20375G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641582 | |||||||
chr12:79641631 | G | A | 1 | a0002c0002t0005g0181 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517-20424C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641631 | |||||||
chr12:79641845 | CA | C | 54 | a0001c0001t0002g0048 a0001c0001t0002g0050 a0001c0001t0002g0054 others(51): Show |
54 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.517-20639delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | |||||||
chr12:79641845 | CAA | C | 84 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(81): Show |
85 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.517-20640_517-2063 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | |||||||
chr12:79641845 | CAAAA | C | 14 | a0002c0002t0001g0168 a0002c0002t0001g0173 a0002c0002t0001g0190 others(11): Show |
14 | HG00673.hp2 HG01074.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.517-20642_517-2063 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | |||||||
chr12:79641845 | CAAAAA | C | 44 | a0002c0002t0001g0169 a0002c0002t0001g0172 a0002c0002t0001g0187 others(41): Show |
44 | HG00544.hp2 HG00621.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.517-20643_517-2063 others(9): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | |||||||
chr12:79641845 | CAAAAAA | C | 37 | a0002c0002t0001g0170 a0002c0002t0001g0171 a0002c0002t0001g0174 others(34): Show |
37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.517-20644_517-2063 others(10): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79641845 | |||||||
chr12:79642030 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-20823G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642030 | |||||||
chr12:79642167 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-20960G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642167 | |||||||
chr12:79642185 | T | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-20978A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642185 | |||||||
chr12:79642252 | T | C | 1 | a0002c0002t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-21045A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642252 | |||||||
chr12:79642378 | AT | A | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-21172delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642378 | |||||||
chr12:79642553 | T | C | 1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.517-21346A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642553 | |||||||
chr12:79642595 | G | A | 1 | a0001c0003t0003g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.517-21388C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642595 | |||||||
chr12:79642742 | C | T | 1 | a0001c0003t0003g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.517-21535G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642742 | |||||||
chr12:79642743 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-21536T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642743 | |||||||
chr12:79642770 | G | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-21563C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642770 | |||||||
chr12:79642844 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-21637C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642844 | |||||||
chr12:79642915 | GA | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21709delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79642915 | |||||||
chr12:79643021 | T | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-21814A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643021 | |||||||
chr12:79643041 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-21834G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643041 | |||||||
chr12:79643137 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21930A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643137 | |||||||
chr12:79643168 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-21961C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643168 | |||||||
chr12:79643211 | A | G | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-22004T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643211 | |||||||
chr12:79643445 | C | A | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-22238G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643445 | |||||||
chr12:79643996 | G | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-22789C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79643996 | |||||||
chr12:79644350 | C | T | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-23143G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644350 | |||||||
chr12:79644659 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-23452A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644659 | |||||||
chr12:79644665 | TAGCAAAA others(3): Show |
T | 1 | a0001c0001t0002g0115 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.517-23468_517-2345 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644665 | |||||||
chr12:79644746 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-23539G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644746 | |||||||
chr12:79644806 | G | T | 2 | a0003c0004t0009g0158 a0003c0004t0009g0159 |
2 | HG01074.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.517-23599C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644806 | |||||||
chr12:79644872 | G | A | 1 | a0002c0002t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-23665C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79644872 | |||||||
chr12:79645007 | AAAG | A | 5 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-23803_517-2380 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645007 | |||||||
chr12:79645036 | C | CCA | 11 | a0001c0001t0002g0106 a0001c0001t0002g0110 a0001c0003t0003g0006 others(8): Show |
11 | HG00621.hp1 HG01074.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-23831_517-2383 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACA | 4 | a0001c0001t0002g0122 a0001c0001t0002g0152 a0001c0003t0023g0147 others(1): Show |
4 | HG01993.hp2 HG02145.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-23833_517-2383 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(1): Show |
42 | a0002c0002t0001g0168 a0002c0002t0001g0171 a0002c0002t0001g0172 others(39): Show |
42 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.517-23837_517-2383 others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(3): Show |
38 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0124 others(35): Show |
38 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.517-23839_517-2383 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(5): Show |
39 | a0001c0001t0002g0115 a0001c0001t0004g0001 a0001c0001t0004g0002 others(36): Show |
40 | HG00423.hp2 HG00639.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-23841_517-2383 others(16): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(7): Show |
7 | a0001c0001t0004g0020 a0001c0001t0004g0031 a0001c0001t0004g0162 others(4): Show |
7 | HG01081.hp2 HG01168.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-23843_517-2383 others(18): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(9): Show |
1 | a0001c0001t0004g0023 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.517-23845_517-2383 others(20): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645036 | C | CCACACAC others(11): Show |
1 | a0002c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-23847_517-2383 others(22): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645036 | |||||||
chr12:79645068 | A | ACACACAC others(6): Show |
1 | a0001c0001t0004g0155 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-23862_517-2386 others(17): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645068 | |||||||
chr12:79645069 | A | C | 46 | a0001c0001t0002g0115 a0001c0001t0004g0001 a0001c0001t0004g0002 others(43): Show |
47 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.517-23862T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645069 | |||||||
chr12:79645070 | A | C | 1 | a0001c0001t0004g0155 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.517-23863T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645070 | |||||||
chr12:79645084 | T | C | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-23877A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645084 | |||||||
chr12:79645399 | G | A | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-24192C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645399 | |||||||
chr12:79645524 | C | G | 2 | a0002c0002t0001g0230 a0002c0002t0019g0178 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-24317G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645524 | |||||||
chr12:79645562 | G | A | 2 | a0003c0004t0009g0156 a0003c0004t0009g0157 |
2 | HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.517-24355C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645562 | |||||||
chr12:79645652 | T | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 |
3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-24445A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645652 | |||||||
chr12:79645673 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-24466A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645673 | |||||||
chr12:79645967 | T | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-24760A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79645967 | |||||||
chr12:79646062 | T | C | 5 | a0001c0003t0002g0154 a0001c0003t0003g0085 a0001c0003t0003g0130 others(2): Show |
5 | HG00544.hp1 NA18967.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-24855A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646062 | |||||||
chr12:79646138 | ATCTTAAA others(4): Show |
A | 1 | a0002c0002t0001g0197 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.517-24942_517-2493 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646138 | |||||||
chr12:79646165 | C | T | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-24958G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646165 | |||||||
chr12:79646314 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-25107A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646314 | |||||||
chr12:79646354 | T | G | 9 | a0001c0001t0004g0001 a0001c0001t0004g0016 a0001c0001t0004g0020 others(6): Show |
10 | HG01081.hp2 HG01109.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-25147A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646354 | |||||||
chr12:79646384 | T | A | 1 | a0001c0003t0023g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.517-25177A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646384 | |||||||
chr12:79646391 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-25184A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646391 | |||||||
chr12:79646506 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-25299A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646506 | |||||||
chr12:79646552 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.517-25345A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646552 | |||||||
chr12:79646704 | G | C | 1 | a0001c0001t0006g0022 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.517-25497C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646704 | |||||||
chr12:79646710 | C | A | 2 | a0001c0003t0003g0144 a0001c0003t0024g0148 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.517-25503G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646710 | |||||||
chr12:79646742 | T | C | 1 | a0002c0002t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.517-25535A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646742 | |||||||
chr12:79646848 | C | A | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.517-25641G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646848 | |||||||
chr12:79646866 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517-25659G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646866 | |||||||
chr12:79646948 | C | T | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-25741G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79646948 | |||||||
chr12:79647173 | CA | C | 95 | a0001c0001t0004g0014 a0002c0002t0001g0168 a0002c0002t0001g0169 others(92): Show |
95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.517-25967delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647173 | |||||||
chr12:79647243 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.517-26036A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647243 | |||||||
chr12:79647759 | A | G | 37 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0171 others(34): Show |
37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.517-26552T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647759 | |||||||
chr12:79647812 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-26605T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647812 | |||||||
chr12:79647852 | A | G | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-26645T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647852 | |||||||
chr12:79647929 | A | G | 3 | a0002c0002t0001g0168 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG03491.hp1 HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.517-26722T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79647929 | |||||||
chr12:79648076 | T | C | 1 | a0002c0002t0001g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-26869A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648076 | |||||||
chr12:79648189 | A | G | 1 | a0001c0001t0010g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.517-26982T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648189 | |||||||
chr12:79648195 | T | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-26988A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648195 | |||||||
chr12:79648318 | A | G | 1 | a0001c0003t0003g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.517-27111T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648318 | |||||||
chr12:79648363 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-27156C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648363 | |||||||
chr12:79648468 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27261G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648468 | |||||||
chr12:79648554 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27347C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648554 | |||||||
chr12:79648557 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27350C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648557 | |||||||
chr12:79648563 | G | A | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-27356C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648563 | |||||||
chr12:79648617 | T | TA | 80 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(77): Show |
81 | HG00423.hp2 HG00639.hp2 HG01074.hp2 others(78): Show |
intron_variant | MODIFIER | c.517-27411dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | |||||||
chr12:79648617 | T | TAA | 16 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0032 others(13): Show |
16 | HG01975.hp2 HG02040.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.517-27412_517-2741 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | |||||||
chr12:79648617 | T | TAAA | 34 | a0001c0001t0004g0034 a0002c0002t0001g0168 a0002c0002t0001g0172 others(31): Show |
34 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-27413_517-2741 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | |||||||
chr12:79648617 | TA | T | 9 | a0001c0001t0002g0056 a0001c0001t0002g0070 a0001c0001t0002g0091 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-27411delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648617 | |||||||
chr12:79648721 | C | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517-27514G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648721 | |||||||
chr12:79648738 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27531T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648738 | |||||||
chr12:79648757 | C | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-27550G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648757 | |||||||
chr12:79648793 | G | GA | 13 | a0001c0001t0002g0070 a0002c0002t0001g0168 a0002c0002t0001g0186 others(10): Show |
13 | HG02071.hp2 HG02145.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.517-27587dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648793 | |||||||
chr12:79648794 | A | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27587T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648794 | |||||||
chr12:79648804 | AT | A | 3 | a0003c0004t0022g0165 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02451.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-27598delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648804 | |||||||
chr12:79648805 | T | A | 95 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(92): Show |
95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.517-27598A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648805 | |||||||
chr12:79648922 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-27715A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79648922 | |||||||
chr12:79649333 | A | T | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-28126T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649333 | |||||||
chr12:79649380 | C | A | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-28173G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649380 | |||||||
chr12:79649596 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-28389C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649596 | |||||||
chr12:79649897 | T | G | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-28690A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79649897 | |||||||
chr12:79650015 | A | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-28808T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650015 | |||||||
chr12:79650147 | C | G | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-28940G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650147 | |||||||
chr12:79650305 | G | GC | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-29099dupG | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650305 | |||||||
chr12:79650387 | C | T | 62 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(59): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-29180G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650387 | |||||||
chr12:79650631 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-29424G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650631 | |||||||
chr12:79650714 | T | TA | 86 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0010 others(83): Show |
86 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.517-29508dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | |||||||
chr12:79650714 | T | TAA | 16 | a0001c0001t0004g0001 a0001c0001t0004g0016 a0001c0001t0004g0020 others(13): Show |
17 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.517-29509_517-2950 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | |||||||
chr12:79650714 | TA | T | 62 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(59): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-29508delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650714 | |||||||
chr12:79650785 | A | G | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-29578T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650785 | |||||||
chr12:79650825 | T | C | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-29618A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79650825 | |||||||
chr12:79651209 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.517-30002G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651209 | |||||||
chr12:79651291 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-30084C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651291 | |||||||
chr12:79651397 | G | A | 2 | a0001c0001t0002g0111 a0001c0001t0002g0114 |
2 | HG00438.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.517-30190C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651397 | |||||||
chr12:79651687 | G | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517-30480C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651687 | |||||||
chr12:79651712 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30505C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651712 | |||||||
chr12:79651713 | G | A | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-30506C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651713 | |||||||
chr12:79651713 | G | T | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-30506C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651713 | |||||||
chr12:79651752 | T | C | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30545A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651752 | |||||||
chr12:79651755 | G | A | 2 | a0002c0002t0001g0211 a0002c0002t0001g0212 |
2 | NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.517-30548C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651755 | |||||||
chr12:79651805 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.517-30598G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651805 | |||||||
chr12:79651836 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-30629C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651836 | |||||||
chr12:79651981 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.517-30774C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79651981 | |||||||
chr12:79652085 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.517-30878C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652085 | |||||||
chr12:79652232 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31025C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652232 | |||||||
chr12:79652509 | G | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-31302C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652509 | |||||||
chr12:79652544 | C | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.517-31337G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652544 | |||||||
chr12:79652576 | A | C | 2 | a0003c0005t0007g0163 a0003c0005t0007g0164 |
2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-31369T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79652576 | |||||||
chr12:79653041 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31834T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653041 | |||||||
chr12:79653057 | T | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-31850A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653057 | |||||||
chr12:79653080 | G | A | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.517-31873C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653080 | |||||||
chr12:79653087 | G | A | 16 | a0001c0003t0002g0154 a0001c0003t0003g0074 a0001c0003t0003g0085 others(13): Show |
16 | HG00544.hp1 HG02056.hp2 HG03491.hp2 others(13): Show |
intron_variant | MODIFIER | c.517-31880C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653087 | |||||||
chr12:79653186 | C | T | 2 | a0002c0002t0001g0177 a0002c0002t0001g0252 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.517-31979G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653186 | |||||||
chr12:79653287 | T | C | 137 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(134): Show |
138 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.517-32080A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653287 | |||||||
chr12:79653362 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-32155C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653362 | |||||||
chr12:79653430 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-32223A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653430 | |||||||
chr12:79653443 | A | C | 7 | a0001c0003t0003g0074 a0001c0003t0003g0132 a0001c0003t0003g0143 others(4): Show |
7 | HG02056.hp2 NA18957.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-32236T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653443 | |||||||
chr12:79653519 | G | T | 1 | a0002c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.517-32312C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653519 | |||||||
chr12:79653543 | G | A | 1 | a0007c0009t0003g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.517-32336C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653543 | |||||||
chr12:79653583 | G | A | 5 | a0002c0002t0001g0190 a0002c0002t0001g0195 a0002c0002t0001g0196 others(2): Show |
5 | HG02027.hp2 HG02071.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-32376C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653583 | |||||||
chr12:79653605 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.517-32398C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653605 | |||||||
chr12:79653657 | T | C | 1 | a0001c0003t0003g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.517-32450A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653657 | |||||||
chr12:79653843 | T | C | 1 | a0001c0001t0004g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.517-32636A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79653843 | |||||||
chr12:79654015 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.517-32808A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654015 | |||||||
chr12:79654032 | A | G | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-32825T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654032 | |||||||
chr12:79654202 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.517-32995C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654202 | |||||||
chr12:79654420 | C | CT | 141 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(138): Show |
142 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(139): Show |
intron_variant | MODIFIER | c.517-33214dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654420 | |||||||
chr12:79654698 | C | T | 62 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(59): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.517-33491G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654698 | |||||||
chr12:79654733 | G | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33526C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654733 | |||||||
chr12:79654774 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-33567A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654774 | |||||||
chr12:79654795 | C | T | 1 | a0001c0003t0003g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-33588G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654795 | |||||||
chr12:79654843 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33636A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79654843 | |||||||
chr12:79655017 | G | A | 1 | a0001c0003t0003g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.517-33810C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655017 | |||||||
chr12:79655042 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.517-33835C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655042 | |||||||
chr12:79655070 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.517-33863T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655070 | |||||||
chr12:79655109 | T | A | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.517-33902A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655109 | |||||||
chr12:79655122 | T | C | 2 | a0002c0002t0001g0230 a0002c0002t0019g0178 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.517-33915A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655122 | |||||||
chr12:79655245 | G | T | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.517-34038C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655245 | |||||||
chr12:79655387 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0237 a0002c0002t0021g0185 |
3 | HG02622.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.517-34180G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655387 | |||||||
chr12:79655410 | T | C | 1 | a0001c0003t0003g0100 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.517-34203A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655410 | |||||||
chr12:79655477 | A | G | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+34252T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655477 | |||||||
chr12:79655611 | C | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+34118G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655611 | |||||||
chr12:79655820 | T | C | 37 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0171 others(34): Show |
37 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.516+33909A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655820 | |||||||
chr12:79655966 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+33763T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79655966 | |||||||
chr12:79656135 | C | T | 1 | a0001c0003t0003g0139 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.516+33594G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656135 | |||||||
chr12:79656185 | A | G | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+33544T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656185 | |||||||
chr12:79656420 | C | T | 10 | a0002c0002t0001g0187 a0002c0002t0001g0189 a0002c0002t0001g0201 others(7): Show |
10 | HG00621.hp2 HG01975.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.516+33309G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656420 | |||||||
chr12:79656654 | T | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+33075A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79656654 | |||||||
chr12:79657420 | T | TA | 7 | a0001c0001t0032g0007 a0003c0004t0009g0156 a0003c0004t0009g0157 others(4): Show |
7 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+32308dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657420 | |||||||
chr12:79657421 | A | T | 35 | a0002c0002t0001g0168 a0002c0002t0001g0187 a0002c0002t0001g0189 others(32): Show |
35 | HG00621.hp2 HG00673.hp2 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.516+32308T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657421 | |||||||
chr12:79657552 | G | A | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+32177C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657552 | |||||||
chr12:79657562 | C | T | 1 | a0001c0001t0004g0016 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.516+32167G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657562 | |||||||
chr12:79657563 | G | A | 1 | a0001c0003t0013g0094 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.516+32166C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657563 | |||||||
chr12:79657635 | C | T | 1 | a0002c0002t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.516+32094G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657635 | |||||||
chr12:79657663 | G | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+32066C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657663 | |||||||
chr12:79657749 | G | A | 4 | a0002c0002t0001g0229 a0003c0005t0007g0004 a0003c0005t0007g0163 others(1): Show |
4 | HG02922.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+31980C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657749 | |||||||
chr12:79657875 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.516+31854A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79657875 | |||||||
chr12:79658020 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+31709A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658020 | |||||||
chr12:79658224 | T | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0092 a0001c0003t0031g0121 |
3 | HG00423.hp1 NA18959.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.516+31505A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658224 | |||||||
chr12:79658436 | T | C | 1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516+31293A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658436 | |||||||
chr12:79658541 | A | G | 2 | a0001c0003t0003g0144 a0001c0003t0024g0148 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.516+31188T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658541 | |||||||
chr12:79658770 | T | C | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+30959A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658770 | |||||||
chr12:79658789 | G | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+30940C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658789 | |||||||
chr12:79658792 | T | C | 1 | a0001c0003t0003g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.516+30937A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658792 | |||||||
chr12:79658880 | T | G | 2 | a0002c0002t0005g0182 a0002c0002t0017g0183 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.516+30849A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79658880 | |||||||
chr12:79659019 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+30710A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659019 | |||||||
chr12:79659043 | A | G | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+30686T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659043 | |||||||
chr12:79659141 | C | T | 2 | a0001c0001t0002g0072 a0001c0001t0026g0055 |
2 | NA18941.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.516+30588G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659141 | |||||||
chr12:79659158 | G | A | 2 | a0002c0002t0001g0214 a0002c0002t0005g0213 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+30571C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659158 | |||||||
chr12:79659165 | C | T | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+30564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659165 | |||||||
chr12:79659166 | G | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+30563C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659166 | |||||||
chr12:79659169 | C | T | 2 | a0002c0002t0001g0175 a0002c0002t0001g0179 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.516+30560G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659169 | |||||||
chr12:79659218 | C | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+30511G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659218 | |||||||
chr12:79659255 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+30474G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659255 | |||||||
chr12:79659297 | GA | G | 5 | a0002c0002t0001g0218 a0003c0004t0009g0156 a0003c0004t0009g0157 others(2): Show |
5 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+30431delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659297 | |||||||
chr12:79659311 | T | C | 1 | a0002c0002t0001g0207 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.516+30418A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659311 | |||||||
chr12:79659442 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+30287A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79659442 | |||||||
chr12:79660170 | T | C | 1 | a0007c0009t0003g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+29559A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660170 | |||||||
chr12:79660185 | A | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+29544T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660185 | |||||||
chr12:79660254 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+29475T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660254 | |||||||
chr12:79660358 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0005g0213 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+29371G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660358 | |||||||
chr12:79660540 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.516+29189G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660540 | |||||||
chr12:79660583 | C | CT | 48 | a0001c0001t0002g0054 a0001c0001t0002g0115 a0001c0001t0003g0053 others(45): Show |
48 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.516+29145dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660583 | |||||||
chr12:79660583 | CT | C | 5 | a0001c0001t0002g0114 a0001c0001t0002g0122 a0002c0002t0005g0250 others(2): Show |
5 | HG01993.hp2 HG02145.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+29145delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660583 | |||||||
chr12:79660906 | A | G | 1 | a0001c0001t0004g0023 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.516+28823T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660906 | |||||||
chr12:79660911 | T | C | 9 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+28818A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79660911 | |||||||
chr12:79661040 | G | C | 1 | a0001c0003t0003g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.516+28689C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661040 | |||||||
chr12:79661148 | C | A | 2 | a0001c0003t0003g0078 a0001c0003t0003g0101 |
2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.516+28581G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661148 | |||||||
chr12:79661206 | G | A | 1 | a0004c0006t0011g0239 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.516+28523C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661206 | |||||||
chr12:79661248 | C | CA | 40 | a0001c0001t0002g0071 a0001c0001t0002g0152 a0001c0001t0004g0023 others(37): Show |
40 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.516+28480dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | |||||||
chr12:79661248 | C | CAA | 9 | a0001c0001t0002g0115 a0001c0003t0003g0078 a0002c0002t0001g0177 others(6): Show |
9 | HG01891.hp2 HG01981.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.516+28479_516+2848 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | |||||||
chr12:79661248 | CA | C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0073 a0001c0001t0004g0127 others(2): Show |
5 | HG01069.hp1 HG01069.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+28480delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661248 | |||||||
chr12:79661347 | T | C | 30 | a0001c0001t0002g0118 a0001c0003t0002g0154 a0001c0003t0003g0074 others(27): Show |
30 | HG00544.hp1 HG02056.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+28382A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661347 | |||||||
chr12:79661355 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+28374T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661355 | |||||||
chr12:79661403 | C | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+28326G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661403 | |||||||
chr12:79661452 | A | G | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+28277T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661452 | |||||||
chr12:79661900 | G | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+27829C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661900 | |||||||
chr12:79661986 | A | G | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+27743T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79661986 | |||||||
chr12:79662191 | A | G | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+27538T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662191 | |||||||
chr12:79662201 | C | CA | 65 | a0001c0001t0002g0080 a0001c0001t0002g0115 a0001c0001t0006g0033 others(62): Show |
65 | HG00544.hp2 HG00673.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.516+27527dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | |||||||
chr12:79662201 | C | CAA | 30 | a0002c0002t0001g0170 a0002c0002t0001g0184 a0002c0002t0001g0187 others(27): Show |
30 | HG00621.hp2 HG00639.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+27526_516+2752 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | |||||||
chr12:79662201 | CA | C | 9 | a0001c0001t0002g0005 a0001c0001t0003g0037 a0001c0001t0003g0038 others(6): Show |
9 | HG01257.hp1 HG02040.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+27527delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662201 | |||||||
chr12:79662246 | C | T | 2 | a0002c0002t0001g0214 a0002c0002t0005g0213 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.516+27483G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662246 | |||||||
chr12:79662334 | C | G | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+27395G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662334 | |||||||
chr12:79662453 | C | A | 1 | a0001c0001t0002g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.516+27276G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662453 | |||||||
chr12:79662523 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+27206T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662523 | |||||||
chr12:79662648 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+27081T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662648 | |||||||
chr12:79662761 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+26968A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662761 | |||||||
chr12:79662813 | T | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+26916A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79662813 | |||||||
chr12:79663355 | T | C | 28 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0174 others(25): Show |
28 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.516+26374A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663355 | |||||||
chr12:79663583 | C | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+26146G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663583 | |||||||
chr12:79663601 | A | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+26128T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663601 | |||||||
chr12:79663770 | C | CA | 7 | a0001c0001t0002g0080 a0001c0001t0002g0117 a0001c0001t0004g0002 others(4): Show |
7 | HG01168.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+25958dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79663770 | |||||||
chr12:79664009 | T | C | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+25720A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664009 | |||||||
chr12:79664131 | T | A | 1 | a0002c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+25598A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664131 | |||||||
chr12:79664132 | C | T | 1 | a0002c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+25597G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664132 | |||||||
chr12:79664137 | A | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+25592T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664137 | |||||||
chr12:79664365 | C | G | 2 | a0001c0001t0002g0118 a0001c0003t0027g0134 |
2 | HG03831.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.516+25364G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664365 | |||||||
chr12:79664411 | C | G | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+25318G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664411 | |||||||
chr12:79664554 | G | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+25175C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664554 | |||||||
chr12:79664658 | C | CG | 105 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(102): Show |
106 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.516+25070dupC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664658 | C | CGG | 49 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0004g0035 others(46): Show |
49 | HG00423.hp2 HG00621.hp2 HG01256.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+25069_516+2507 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664658 | C | CGGG | 25 | a0002c0002t0001g0170 a0002c0002t0001g0179 a0002c0002t0001g0180 others(22): Show |
25 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+25068_516+2507 others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664658 | C | CGGGG | 16 | a0002c0002t0001g0169 a0002c0002t0001g0174 a0002c0002t0001g0175 others(13): Show |
16 | HG01261.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.516+25067_516+2507 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664658 | C | CGGGGGGG others(3): Show |
1 | a0003c0005t0007g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516+25070_516+2507 others(14): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664658 | C | CGGGGGGG others(4): Show |
2 | a0003c0005t0007g0004 a0003c0005t0007g0163 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+25070_516+2507 others(15): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664658 | |||||||
chr12:79664662 | G | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+25067C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79664662 | |||||||
chr12:79665417 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24312A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665417 | |||||||
chr12:79665498 | A | G | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+24231T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665498 | |||||||
chr12:79665541 | A | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+24188T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665541 | |||||||
chr12:79665651 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+24078A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665651 | |||||||
chr12:79665661 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24068T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665661 | |||||||
chr12:79665679 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+24050A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665679 | |||||||
chr12:79665848 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.516+23881A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665848 | |||||||
chr12:79665850 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+23879A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665850 | |||||||
chr12:79665994 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+23735G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79665994 | |||||||
chr12:79666125 | A | G | 1 | a0001c0003t0003g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+23604T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666125 | |||||||
chr12:79666700 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.516+23029A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666700 | |||||||
chr12:79666818 | A | G | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+22911T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666818 | |||||||
chr12:79666833 | T | C | 2 | a0002c0002t0001g0225 a0002c0002t0012g0220 |
2 | NA18946.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.516+22896A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666833 | |||||||
chr12:79666985 | T | C | 2 | a0001c0001t0004g0010 a0001c0001t0004g0011 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.516+22744A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79666985 | |||||||
chr12:79667295 | C | G | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+22434G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667295 | |||||||
chr12:79667299 | G | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+22430C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667299 | |||||||
chr12:79667506 | CTG | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+22221_516+2222 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667506 | |||||||
chr12:79667576 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+22153A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667576 | |||||||
chr12:79667601 | A | C | 1 | a0002c0002t0012g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.516+22128T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667601 | |||||||
chr12:79667632 | T | G | 2 | a0001c0001t0010g0126 a0002c0002t0005g0250 |
2 | HG02896.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.516+22097A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667632 | |||||||
chr12:79667713 | G | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+22016C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667713 | |||||||
chr12:79667846 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0133 |
2 | HG00673.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.516+21883A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667846 | |||||||
chr12:79667863 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+21866C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667863 | |||||||
chr12:79667925 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.516+21804G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667925 | |||||||
chr12:79667942 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+21787A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79667942 | |||||||
chr12:79668081 | T | C | 6 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0028 others(3): Show |
6 | NA18942.hp1 NA18945.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+21648A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668081 | |||||||
chr12:79668104 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+21625A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668104 | |||||||
chr12:79668376 | T | C | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+21353A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668376 | |||||||
chr12:79668450 | A | G | 236 | a0001c0001t0002g0005 a0001c0001t0002g0041 a0001c0001t0002g0042 others(233): Show |
237 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.516+21279T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668450 | |||||||
chr12:79668458 | C | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+21271G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668458 | |||||||
chr12:79668545 | T | C | 40 | a0002c0002t0001g0168 a0002c0002t0001g0172 a0002c0002t0001g0173 others(37): Show |
40 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+21184A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668545 | |||||||
chr12:79668581 | C | T | 1 | a0001c0001t0004g0124 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.516+21148G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668581 | |||||||
chr12:79668765 | T | TGCTCACC | 4 | a0001c0001t0004g0127 a0001c0001t0010g0125 a0001c0001t0010g0126 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+20957_516+2096 others(11): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79668765 | |||||||
chr12:79669231 | G | C | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+20498C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669231 | |||||||
chr12:79669271 | T | C | 11 | a0002c0002t0001g0241 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01109.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+20458A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669271 | |||||||
chr12:79669335 | A | G | 1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+20394T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669335 | |||||||
chr12:79669494 | A | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+20235T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669494 | |||||||
chr12:79669517 | C | T | 3 | a0001c0001t0010g0125 a0001c0001t0010g0126 a0001c0001t0010g0128 |
3 | NA18968.hp2 NA18987.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.516+20212G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79669517 | |||||||
chr12:79670058 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+19671C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670058 | |||||||
chr12:79670212 | A | C | 1 | a0001c0003t0003g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.516+19517T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670212 | |||||||
chr12:79670355 | C | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+19374G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670355 | |||||||
chr12:79670465 | GA | G | 28 | a0001c0001t0002g0050 a0001c0003t0031g0121 a0002c0002t0001g0169 others(25): Show |
28 | HG00423.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.516+19263delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670465 | |||||||
chr12:79670586 | A | T | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+19143T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670586 | |||||||
chr12:79670702 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.516+19027C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670702 | |||||||
chr12:79670732 | A | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+18997T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670732 | |||||||
chr12:79670873 | AG | A | 3 | a0002c0002t0001g0217 a0005c0007t0033g0255 a0005c0007t0034g0254 |
3 | HG02145.hp1 HG02976.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.516+18855delC | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670873 | |||||||
chr12:79670877 | G | T | 95 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(92): Show |
95 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.516+18852C>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79670877 | |||||||
chr12:79671053 | C | G | 1 | a0001c0001t0002g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.516+18676G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671053 | |||||||
chr12:79671086 | T | C | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+18643A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671086 | |||||||
chr12:79671123 | T | TA | 9 | a0001c0001t0002g0080 a0002c0002t0001g0217 a0002c0002t0001g0218 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+18605dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671123 | |||||||
chr12:79671123 | TA | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(6): Show |
9 | HG01074.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+18605delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671123 | |||||||
chr12:79671160 | C | T | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+18569G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671160 | |||||||
chr12:79671406 | T | C | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+18323A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671406 | |||||||
chr12:79671418 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+18311C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671418 | |||||||
chr12:79671536 | T | G | 39 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(36): Show |
40 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.516+18193A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671536 | |||||||
chr12:79671636 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+18093G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671636 | |||||||
chr12:79671699 | T | C | 1 | a0001c0003t0003g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.516+18030A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671699 | |||||||
chr12:79671726 | A | G | 7 | a0001c0003t0002g0154 a0001c0003t0003g0085 a0001c0003t0003g0130 others(4): Show |
7 | HG00544.hp1 NA18967.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+18003T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79671726 | |||||||
chr12:79672005 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+17724A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672005 | |||||||
chr12:79672095 | G | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+17634C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672095 | |||||||
chr12:79672142 | C | T | 1 | a0001c0001t0029g0119 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.516+17587G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672142 | |||||||
chr12:79672165 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+17564G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672165 | |||||||
chr12:79672177 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+17552C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672177 | |||||||
chr12:79672299 | A | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+17430T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672299 | |||||||
chr12:79672400 | C | T | 98 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(95): Show |
98 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.516+17329G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672400 | |||||||
chr12:79672657 | TTGTG | T | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+17068_516+1707 others(8): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672657 | |||||||
chr12:79672918 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+16811T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79672918 | |||||||
chr12:79673213 | G | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+16516C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673213 | |||||||
chr12:79673218 | T | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+16511A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673218 | |||||||
chr12:79673358 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+16371G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673358 | |||||||
chr12:79673507 | A | G | 1 | a0001c0001t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.516+16222T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673507 | |||||||
chr12:79673802 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.516+15927G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79673802 | |||||||
chr12:79674250 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+15479G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674250 | |||||||
chr12:79674388 | TA | T | 58 | a0001c0001t0004g0014 a0002c0002t0001g0168 a0002c0002t0001g0172 others(55): Show |
58 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.516+15340delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674388 | |||||||
chr12:79674389 | A | T | 1 | a0001c0003t0003g0006 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.516+15340T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674389 | |||||||
chr12:79674423 | C | T | 1 | a0003c0005t0007g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.516+15306G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674423 | |||||||
chr12:79674575 | G | C | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+15154C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674575 | |||||||
chr12:79674729 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+15000G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674729 | |||||||
chr12:79674783 | C | T | 1 | a0001c0003t0003g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.516+14946G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674783 | |||||||
chr12:79674909 | C | T | 7 | a0001c0001t0002g0118 a0001c0003t0008g0135 a0001c0003t0008g0136 others(4): Show |
7 | HG03831.hp2 NA18946.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+14820G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79674909 | |||||||
chr12:79675001 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+14728C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675001 | |||||||
chr12:79675452 | C | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+14277G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675452 | |||||||
chr12:79675619 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+14110G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675619 | |||||||
chr12:79675882 | T | C | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+13847A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675882 | |||||||
chr12:79675990 | G | A | 6 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(3): Show |
6 | HG01074.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+13739C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79675990 | |||||||
chr12:79676023 | C | T | 1 | a0002c0002t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+13706G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676023 | |||||||
chr12:79676030 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+13699T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676030 | |||||||
chr12:79676236 | T | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+13493A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676236 | |||||||
chr12:79676240 | G | C | 1 | a0001c0003t0008g0150 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.516+13489C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676240 | |||||||
chr12:79676380 | T | G | 1 | a0005c0007t0033g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516+13349A>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676380 | |||||||
chr12:79676505 | A | G | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+13224T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676505 | |||||||
chr12:79676659 | C | T | 1 | a0001c0003t0028g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.516+13070G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676659 | |||||||
chr12:79676754 | C | T | 2 | a0001c0003t0003g0045 a0001c0003t0003g0082 |
2 | HG01069.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.516+12975G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676754 | |||||||
chr12:79676758 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+12971G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79676758 | |||||||
chr12:79677022 | T | C | 1 | a0007c0009t0003g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+12707A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677022 | |||||||
chr12:79677157 | A | T | 1 | a0001c0001t0002g0042 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+12572T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677157 | |||||||
chr12:79677216 | A | G | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+12513T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677216 | |||||||
chr12:79677419 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516+12310A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677419 | |||||||
chr12:79677861 | A | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+11868T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677861 | |||||||
chr12:79677873 | A | G | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11856T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677873 | |||||||
chr12:79677911 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+11818G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677911 | |||||||
chr12:79677944 | T | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11785A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79677944 | |||||||
chr12:79678072 | T | C | 4 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0124 others(1): Show |
4 | HG02040.hp2 HG02080.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+11657A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678072 | |||||||
chr12:79678175 | G | A | 82 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(79): Show |
82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+11554C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678175 | |||||||
chr12:79678357 | C | T | 1 | a0001c0003t0003g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.516+11372G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678357 | |||||||
chr12:79678609 | A | C | 1 | a0001c0003t0014g0161 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.516+11120T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678609 | |||||||
chr12:79678663 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+11066G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678663 | |||||||
chr12:79678853 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+10876C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678853 | |||||||
chr12:79678868 | A | AT | 141 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0090 others(138): Show |
142 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.516+10860dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678868 | |||||||
chr12:79678868 | A | ATT | 100 | a0001c0001t0002g0005 a0001c0001t0002g0042 a0001c0001t0002g0043 others(97): Show |
100 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.516+10859_516+1086 others(6): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79678868 | |||||||
chr12:79679052 | T | C | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+10677A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679052 | |||||||
chr12:79679088 | C | A | 1 | a0007c0009t0003g0151 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.516+10641G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679088 | |||||||
chr12:79679613 | A | C | 1 | a0001c0001t0004g0012 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+10116T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679613 | |||||||
chr12:79679622 | C | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG01192.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.516+10107G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679622 | |||||||
chr12:79679623 | C | T | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+10106G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679623 | |||||||
chr12:79679634 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+10095T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679634 | |||||||
chr12:79679897 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.516+9832C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679897 | |||||||
chr12:79679918 | A | G | 40 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(37): Show |
41 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+9811T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679918 | |||||||
chr12:79679960 | A | G | 1 | a0002c0002t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.516+9769T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679960 | |||||||
chr12:79679995 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+9734A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79679995 | |||||||
chr12:79680014 | G | A | 14 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(11): Show |
14 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.516+9715C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680014 | |||||||
chr12:79680020 | C | T | 31 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0174 others(28): Show |
31 | HG00639.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.516+9709G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680020 | |||||||
chr12:79680094 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+9635T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680094 | |||||||
chr12:79680127 | A | G | 82 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(79): Show |
82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+9602T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680127 | |||||||
chr12:79680274 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+9455G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680274 | |||||||
chr12:79680305 | C | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+9424G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680305 | |||||||
chr12:79680405 | A | G | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+9324T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680405 | |||||||
chr12:79680941 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.516+8788G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79680941 | |||||||
chr12:79681028 | T | C | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+8701A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681028 | |||||||
chr12:79681042 | G | C | 1 | a0002c0002t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+8687C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681042 | |||||||
chr12:79681045 | G | C | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+8684C>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681045 | |||||||
chr12:79681126 | A | AGGGAGGG others(3): Show |
2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+8593_516+8602d others(12): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681126 | |||||||
chr12:79681137 | G | A | 1 | a0001c0001t0032g0007 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+8592C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681137 | |||||||
chr12:79681145 | TGGGGA | T | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+8579_516+8583d others(7): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681145 | |||||||
chr12:79681688 | A | C | 1 | a0001c0003t0003g0045 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.516+8041T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681688 | |||||||
chr12:79681695 | C | CT | 4 | a0002c0002t0001g0241 a0002c0002t0005g0242 a0003c0004t0007g0166 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+8033dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681695 | |||||||
chr12:79681789 | G | A | 1 | a0001c0001t0006g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.516+7940C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681789 | |||||||
chr12:79681981 | T | C | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.516+7748A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79681981 | |||||||
chr12:79682161 | A | G | 5 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+7568T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682161 | |||||||
chr12:79682221 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.516+7508C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682221 | |||||||
chr12:79682286 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.516+7443C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682286 | |||||||
chr12:79682504 | T | C | 1 | a0002c0002t0001g0235 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.516+7225A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682504 | |||||||
chr12:79682638 | T | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+7091A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682638 | |||||||
chr12:79682946 | A | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0011 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.516+6783T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79682946 | |||||||
chr12:79683593 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+6136G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683593 | |||||||
chr12:79683605 | C | CT | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0003c0004t0009g0156 others(2): Show |
5 | HG02896.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+6123dupA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683605 | |||||||
chr12:79683605 | CT | C | 11 | a0001c0001t0002g0120 a0001c0001t0004g0034 a0001c0001t0010g0128 others(8): Show |
11 | HG01074.hp2 HG01099.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+6123delA | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683605 | |||||||
chr12:79683621 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.516+6108A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683621 | |||||||
chr12:79683692 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+6037C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683692 | |||||||
chr12:79683752 | C | A | 1 | a0001c0003t0031g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.516+5977G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683752 | |||||||
chr12:79683895 | G | A | 4 | a0001c0001t0004g0127 a0001c0001t0010g0125 a0001c0001t0010g0126 others(1): Show |
4 | NA18941.hp1 NA18968.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5834C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683895 | |||||||
chr12:79683930 | G | A | 2 | a0003c0004t0007g0166 a0003c0004t0007g0167 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.516+5799C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79683930 | |||||||
chr12:79684084 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG02523.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.516+5645G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684084 | |||||||
chr12:79684183 | A | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+5546T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684183 | |||||||
chr12:79684292 | TA | T | 9 | a0002c0002t0001g0171 a0003c0004t0009g0156 a0003c0004t0009g0157 others(6): Show |
9 | HG01074.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+5436delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684292 | |||||||
chr12:79684303 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516+5426A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684303 | |||||||
chr12:79684448 | T | C | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+5281A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684448 | |||||||
chr12:79684540 | G | A | 1 | a0001c0003t0002g0154 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.516+5189C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684540 | |||||||
chr12:79684614 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+5115G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684614 | |||||||
chr12:79684636 | G | GA | 4 | a0002c0002t0001g0222 a0002c0002t0001g0223 a0002c0002t0001g0224 others(1): Show |
4 | HG00621.hp2 HG04115.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5092dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684636 | |||||||
chr12:79684644 | C | G | 97 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0171 others(94): Show |
97 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.516+5085G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684644 | |||||||
chr12:79684856 | G | A | 1 | a0001c0001t0004g0035 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.516+4873C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79684856 | |||||||
chr12:79685182 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG01192.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.516+4547T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685182 | |||||||
chr12:79685268 | G | A | 140 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(137): Show |
141 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.516+4461C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685268 | |||||||
chr12:79685304 | T | C | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+4425A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685304 | |||||||
chr12:79685350 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+4379T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685350 | |||||||
chr12:79685525 | G | A | 1 | a0004c0006t0011g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+4204C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685525 | |||||||
chr12:79685546 | T | C | 1 | a0002c0002t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.516+4183A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685546 | |||||||
chr12:79685803 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+3926C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685803 | |||||||
chr12:79685961 | C | A | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+3768G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79685961 | |||||||
chr12:79686441 | C | G | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+3288G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686441 | |||||||
chr12:79686463 | T | C | 1 | a0002c0002t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516+3266A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686463 | |||||||
chr12:79686782 | T | C | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+2947A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686782 | |||||||
chr12:79686811 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.516+2918T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686811 | |||||||
chr12:79686838 | T | C | 83 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(80): Show |
83 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.516+2891A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79686838 | |||||||
chr12:79687174 | G | A | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+2555C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687174 | |||||||
chr12:79687214 | C | T | 1 | a0001c0003t0013g0040 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.516+2515G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687214 | |||||||
chr12:79687301 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+2428T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687301 | |||||||
chr12:79687391 | A | T | 1 | a0003c0004t0022g0165 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+2338T>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687391 | |||||||
chr12:79687409 | A | C | 1 | a0001c0001t0006g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.516+2320T>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687409 | |||||||
chr12:79687589 | T | C | 3 | a0004c0006t0011g0238 a0004c0006t0011g0239 a0004c0006t0011g0240 |
3 | HG02258.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.516+2140A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687589 | |||||||
chr12:79687601 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02630.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.516+2128A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687601 | |||||||
chr12:79687615 | T | A | 1 | a0002c0002t0001g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.516+2114A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687615 | |||||||
chr12:79687846 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+1883C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79687846 | |||||||
chr12:79688029 | C | T | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+1700G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688029 | |||||||
chr12:79688200 | C | A | 1 | a0002c0002t0001g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.516+1529G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688200 | |||||||
chr12:79688227 | T | TA | 40 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(37): Show |
41 | HG00423.hp2 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+1501dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688227 | |||||||
chr12:79688321 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG02572.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.516+1408T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688321 | |||||||
chr12:79688467 | T | TA | 27 | a0001c0001t0002g0133 a0001c0001t0002g0152 a0001c0001t0002g0153 others(24): Show |
27 | HG00544.hp1 HG00673.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.516+1261dupT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688467 | |||||||
chr12:79688467 | TA | T | 112 | a0001c0001t0002g0005 a0001c0001t0004g0001 a0001c0001t0004g0002 others(109): Show |
113 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.516+1261delT | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688467 | |||||||
chr12:79688708 | T | A | 4 | a0003c0004t0009g0156 a0003c0004t0009g0157 a0003c0004t0009g0158 others(1): Show |
4 | HG01074.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+1021A>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688708 | |||||||
chr12:79688935 | C | G | 1 | a0005c0007t0034g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.516+794G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688935 | |||||||
chr12:79688985 | T | TAAC | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+741_516+743dup others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79688985 | |||||||
chr12:79689126 | G | A | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.516+603C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689126 | |||||||
chr12:79689355 | TGTC | T | 3 | a0003c0005t0007g0004 a0003c0005t0007g0163 a0003c0005t0007g0164 |
3 | HG02922.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.516+371_516+373del others(3): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689355 | |||||||
chr12:79689397 | ACAGCCAA others(16): Show |
A | 2 | a0001c0003t0003g0160 a0001c0003t0014g0161 |
2 | NA18942.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.516+309_516+331del others(23): Show |
PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689397 | |||||||
chr12:79689512 | C | G | 82 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(79): Show |
82 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.516+217G>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689512 | |||||||
chr12:79689524 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.516+205C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689524 | |||||||
chr12:79689644 | C | T | 2 | a0001c0001t0004g0002 a0001c0001t0004g0003 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.516+85G>A | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 2/6 | chr12 | 79689644 | |||||||
chr12:79690423 | G | A | 11 | a0002c0002t0001g0241 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01109.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-147-32C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690423 | |||||||
chr12:79690570 | C | A | 1 | a0001c0001t0004g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-147-179G>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690570 | |||||||
chr12:79690596 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-147-205C>T | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690596 | |||||||
chr12:79690648 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-148+224T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690648 | |||||||
chr12:79690683 | T | C | 92 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 others(89): Show |
92 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-148+189A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690683 | |||||||
chr12:79690726 | T | C | 1 | a0001c0003t0003g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-148+146A>G | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690726 | |||||||
chr12:79690729 | A | G | 2 | a0005c0007t0033g0255 a0005c0007t0034g0254 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-148+143T>C | PAWR | ENSG00000177425.11 | transcript | ENST00000328827.9 | protein_coding | 1/6 | chr12 | 79690729 |