Item | Value |
---|---|
geneid | 1525 |
ensemblid | ENSG00000154639.19 |
hgncid | 2559 |
symbol | CXADR |
name | CXADR Ig-like cell adhesion molecule |
refseq_nuc | NM_001338.5 |
refseq_prot | NP_001329.1 |
ensembl_nuc | ENST00000284878.12 |
ensembl_prot | ENSP00000284878.7 |
mane_status | MANE Select |
chr | chr21 |
start | 17513043 |
end | 17570100 |
strand | + |
ver | v1.2 |
region | chr21:17513043-17570100 |
region5000 | chr21:17508043-17575100 |
regionname0 | CXADR_chr21_17513043_17570100 |
regionname5000 | CXADR_chr21_17508043_17575100 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 365 | 343 | 88 | 56 | 143 | 12 | 42 | 97 | CXADR_chr21_17508043_17575100 | CXADR | MALLL others(360): Show |
chr21 | 17508043 | 17575100 |
a0002 | 0/0 | 365 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | MALLL others(360): Show |
chr21 | 17508043 | 17575100 |
a0003 | 0/0 | 365 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | MALLL others(360): Show |
chr21 | 17508043 | 17575100 |
a0004 | 0/0 | 365 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CXADR_chr21_17508043_17575100 | CXADR | MALLL others(360): Show |
chr21 | 17508043 | 17575100 |
a0005 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | MALLL others(360): Show |
chr21 | 17508043 | 17575100 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1095 | 250 | 40 | 45 | 113 | 12 | 39 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0002 | 0/1 | 1095 | 67 | 25 | 8 | 30 | 0 | 3 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0003 | 0/0 | 1095 | 9 | 8 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0004 | 0/0 | 1095 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0006 | 0/0 | 1095 | 3 | 2 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0007 | 0/0 | 1095 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0009 | 0/0 | 1095 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0011 | 0/0 | 1095 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0001c0013 | 0/0 | 1095 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0002c0005 | 0/0 | 1095 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0003c0010 | 0/0 | 1095 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0004c0008 | 0/0 | 1095 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 | ||
a0005c0012 | 0/0 | 1095 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | ATGGC others(1090): Show |
chr21 | 17508043 | 17575100 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5595 | 74 | 3 | 13 | 44 | 4 | 10 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0002 | 0/0 | 5594 | 49 | 14 | 3 | 19 | 1 | 12 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0003 | 0/0 | 5592 | 47 | 4 | 10 | 23 | 1 | 9 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0005 | 0/0 | 5594 | 12 | 8 | 4 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0007 | 0/0 | 5595 | 9 | 0 | 5 | 1 | 1 | 2 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0012 | 0/0 | 5595 | 5 | 0 | 0 | 5 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0015 | 0/0 | 5594 | 3 | 0 | 1 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0016 | 0/0 | 5589 | 2 | 0 | 0 | 1 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5584): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0017 | 0/0 | 5593 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0019 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0022 | 0/0 | 5595 | 2 | 0 | 1 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0023 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0024 | 0/0 | 5596 | 2 | 0 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5591): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0025 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5591): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0026 | 0/0 | 5595 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0028 | 0/0 | 5593 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0029 | 0/0 | 5591 | 2 | 0 | 0 | 1 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0030 | 0/0 | 5593 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0031 | 0/0 | 5594 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0033 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0041 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0042 | 0/0 | 5594 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0043 | 0/0 | 5594 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0044 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0045 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0046 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0047 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0048 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0049 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0050 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5591): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0051 | 0/0 | 5597 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5592): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0052 | 0/0 | 5595 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0053 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0054 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0055 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0056 | 0/0 | 5594 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0058 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0065 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0066 | 0/0 | 5591 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0067 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0068 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5584): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0076 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0079 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0080 | 1/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0001t0081 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0004 | 0/0 | 5593 | 11 | 0 | 0 | 11 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0006 | 0/0 | 5592 | 10 | 8 | 2 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0008 | 0/0 | 5591 | 8 | 0 | 0 | 7 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0010 | 0/1 | 5593 | 6 | 2 | 2 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0011 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5581): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0013 | 0/0 | 5594 | 4 | 4 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0014 | 0/0 | 5593 | 4 | 3 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0020 | 0/0 | 5591 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0021 | 0/0 | 5591 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0027 | 0/0 | 5591 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0034 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0035 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0037 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0038 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0039 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0057 | 0/0 | 5590 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5585): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0059 | 0/0 | 5588 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5583): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0060 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5584): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0061 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5591): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0062 | 0/0 | 5591 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0070 | 0/0 | 5594 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0071 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0072 | 0/0 | 5590 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5585): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0073 | 0/0 | 5591 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0083 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0085 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0001c0002t0086 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0003t0009 | 0/0 | 5594 | 7 | 7 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0003t0016 | 0/0 | 5589 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5584): Show |
chr21 | 17508043 | 17575100 |
a0001c0003t0064 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0001c0004t0011 | 0/0 | 5586 | 5 | 5 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5581): Show |
chr21 | 17508043 | 17575100 |
a0001c0004t0040 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5581): Show |
chr21 | 17508043 | 17575100 |
a0001c0004t0069 | 0/0 | 5591 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5586): Show |
chr21 | 17508043 | 17575100 |
a0001c0006t0032 | 0/0 | 5594 | 2 | 1 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0006t0078 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0007t0002 | 0/0 | 5594 | 2 | 2 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0001c0007t0033 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0009t0074 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
a0001c0009t0075 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0011t0063 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0001c0013t0010 | 0/0 | 5593 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0002c0005t0018 | 0/0 | 5594 | 3 | 3 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5589): Show |
chr21 | 17508043 | 17575100 |
a0002c0005t0077 | 0/0 | 5593 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0003c0010t0004 | 0/0 | 5593 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0003c0010t0036 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0004c0008t0082 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5587): Show |
chr21 | 17508043 | 17575100 |
a0004c0008t0084 | 0/0 | 5593 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5588): Show |
chr21 | 17508043 | 17575100 |
a0005c0012t0001 | 0/0 | 5595 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | AGTCG others(5590): Show |
chr21 | 17508043 | 17575100 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0012g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0015g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0016g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0016g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0019g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0019g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0022g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0022g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0023g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0023g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0024g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0024g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0025g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0026g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0026g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0028g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0028g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0029g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0029g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0030g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0030g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0031g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0031g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0033g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0041g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0042g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0043g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0044g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0045g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0046g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0047g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0048g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0049g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0050g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0051g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0052g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0053g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0054g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0055g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0056g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0058g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0065g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0066g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0067g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0068g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0076g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0079g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0080g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0001t0081g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0296 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0010g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0020g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0020g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0021g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0021g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0027g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0034g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0035g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0037g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0038g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0039g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0057g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0059g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0060g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0061g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0062g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0070g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0071g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0072g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0073g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0083g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0085g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0002t0086g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0016g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0003t0064g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0040g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0004t0069g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0032g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0032g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0006t0078g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0007t0033g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0009t0074g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0009t0075g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0011t0063g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0001c0013t0010g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0002c0005t0077g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0003c0010t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0003c0010t0036g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0004c0008t0082g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0004c0008t0084g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
a0005c0012t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0314 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00140 | hp2 | a0001 | c0001 | t0052 | g0044 | EUR | GBR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00323 | hp1 | a0001 | c0001 | t0042 | g0270 | EUR | FIN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00423 | hp1 | a0001 | c0001 | t0025 | g0249 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0322 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0321 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00639 | hp1 | a0001 | c0002 | t0006 | g0099 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00639 | hp2 | a0001 | c0001 | t0045 | g0261 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00642 | hp1 | a0001 | c0002 | t0014 | g0074 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0258 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00673 | hp2 | a0001 | c0002 | t0035 | g0337 | EAS | CHS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0233 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00741 | hp1 | a0001 | c0001 | t0022 | g0259 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01069 | hp1 | a0001 | c0001 | t0054 | g0239 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01074 | hp1 | a0001 | c0001 | t0043 | g0117 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01074 | hp2 | a0001 | c0002 | t0083 | g0122 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01081 | hp2 | a0001 | c0001 | t0065 | g0062 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01099 | hp1 | a0001 | c0002 | t0086 | g0001 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01109 | hp2 | a0001 | c0006 | t0032 | g0014 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01175 | hp1 | a0001 | c0013 | t0010 | g0295 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01192 | hp2 | a0001 | c0002 | t0006 | g0001 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01243 | hp1 | a0001 | c0003 | t0016 | g0184 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0214 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01258 | hp1 | a0001 | c0001 | t0047 | g0262 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0215 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01346 | hp1 | a0001 | c0002 | t0010 | g0225 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0010 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01361 | hp2 | a0001 | c0001 | t0024 | g0254 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01433 | hp1 | a0001 | c0002 | t0010 | g0313 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01496 | hp1 | a0001 | c0001 | t0015 | g0251 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0199 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01884 | hp2 | a0001 | c0002 | t0011 | g0105 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0101 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01975 | hp1 | a0001 | c0002 | t0027 | g0142 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02015 | hp2 | a0001 | c0002 | t0034 | g0329 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02027 | hp1 | a0005 | c0012 | t0001 | g0279 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02027 | hp2 | a0001 | c0002 | t0008 | g0042 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02055 | hp1 | a0001 | c0001 | t0028 | g0088 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02056 | hp2 | a0001 | c0002 | t0008 | g0158 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0319 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02074 | hp1 | a0001 | c0002 | t0004 | g0339 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02074 | hp2 | a0001 | c0002 | t0021 | g0331 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02080 | hp2 | a0001 | c0001 | t0019 | g0320 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02129 | hp1 | a0001 | c0001 | t0046 | g0203 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0230 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0100 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02145 | hp2 | a0001 | c0001 | t0079 | g0077 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02155 | hp1 | a0003 | c0010 | t0004 | g0340 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CDX | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02257 | hp2 | a0001 | c0002 | t0013 | g0102 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02258 | hp1 | a0001 | c0001 | t0028 | g0089 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02258 | hp2 | a0002 | c0005 | t0018 | g0150 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02273 | hp1 | a0001 | c0001 | t0030 | g0163 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02280 | hp1 | a0001 | c0002 | t0013 | g0104 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02280 | hp2 | a0001 | c0004 | t0069 | g0303 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02300 | hp2 | a0001 | c0001 | t0024 | g0208 | AMR | PEL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02451 | hp2 | a0001 | c0006 | t0078 | g0012 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02523 | hp1 | a0001 | c0002 | t0021 | g0330 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02572 | hp2 | a0001 | c0004 | t0011 | g0041 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0115 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02622 | hp1 | a0001 | c0004 | t0011 | g0185 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02622 | hp2 | a0002 | c0005 | t0018 | g0152 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02630 | hp1 | a0001 | c0003 | t0009 | g0179 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02630 | hp2 | a0001 | c0001 | t0067 | g0015 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02698 | hp1 | a0001 | c0002 | t0010 | g0308 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0234 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02717 | hp1 | a0001 | c0007 | t0002 | g0090 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0086 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02723 | hp1 | a0001 | c0002 | t0013 | g0103 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02723 | hp2 | a0001 | c0002 | t0006 | g0001 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0232 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02738 | hp1 | a0001 | c0001 | t0051 | g0204 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0048 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0149 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02895 | hp1 | a0002 | c0005 | t0077 | g0147 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02895 | hp2 | a0001 | c0002 | t0085 | g0073 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02896 | hp1 | a0001 | c0003 | t0064 | g0145 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02896 | hp2 | a0001 | c0001 | t0017 | g0175 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02897 | hp1 | a0001 | c0002 | t0014 | g0076 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02897 | hp2 | a0001 | c0003 | t0009 | g0151 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02922 | hp1 | a0001 | c0002 | t0014 | g0078 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02922 | hp2 | a0001 | c0002 | t0006 | g0144 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02965 | hp2 | a0001 | c0001 | t0017 | g0096 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02970 | hp1 | a0001 | c0002 | t0061 | g0016 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0299 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02976 | hp2 | a0001 | c0009 | t0075 | g0187 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03041 | hp2 | a0001 | c0004 | t0011 | g0079 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03098 | hp1 | a0002 | c0005 | t0018 | g0143 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03139 | hp2 | a0001 | c0004 | t0040 | g0316 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03195 | hp2 | a0001 | c0006 | t0032 | g0013 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03209 | hp2 | a0001 | c0001 | t0031 | g0182 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0091 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03225 | hp2 | a0001 | c0002 | t0060 | g0005 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03486 | hp2 | a0001 | c0002 | t0027 | g0018 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03490 | hp1 | a0004 | c0008 | t0082 | g0309 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03490 | hp2 | a0001 | c0001 | t0066 | g0054 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03492 | hp1 | a0004 | c0008 | t0084 | g0310 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03516 | hp1 | a0001 | c0001 | t0031 | g0183 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03516 | hp2 | a0001 | c0003 | t0009 | g0024 | AFR | ESN | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03540 | hp1 | a0001 | c0011 | t0063 | g0159 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03540 | hp2 | a0001 | c0009 | t0074 | g0188 | AFR | GWD | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03654 | hp1 | a0001 | c0001 | t0048 | g0228 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03654 | hp2 | a0001 | c0002 | t0070 | g0028 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03704 | hp2 | a0001 | c0001 | t0015 | g0265 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04184 | hp1 | a0001 | c0001 | t0058 | g0243 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04184 | hp2 | a0001 | c0002 | t0008 | g0047 | SAS | BEB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18522 | hp2 | a0001 | c0003 | t0009 | g0023 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18747 | hp2 | a0001 | c0001 | t0025 | g0008 | EAS | CHB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18906 | hp1 | a0001 | c0002 | t0013 | g0106 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18906 | hp2 | a0001 | c0007 | t0033 | g0186 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18940 | hp2 | a0001 | c0001 | t0041 | g0256 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18941 | hp1 | a0001 | c0002 | t0008 | g0061 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18941 | hp2 | a0001 | c0001 | t0055 | g0305 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18944 | hp1 | a0001 | c0001 | t0076 | g0291 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18947 | hp1 | a0001 | c0001 | t0023 | g0238 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18948 | hp1 | a0001 | c0002 | t0008 | g0003 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18966 | hp2 | a0001 | c0001 | t0026 | g0241 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18967 | hp1 | a0001 | c0002 | t0004 | g0334 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18967 | hp2 | a0001 | c0001 | t0068 | g0029 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18970 | hp2 | a0001 | c0001 | t0081 | g0162 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18971 | hp1 | a0001 | c0002 | t0037 | g0323 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18975 | hp2 | a0001 | c0001 | t0050 | g0216 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18977 | hp2 | a0001 | c0001 | t0016 | g0068 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18981 | hp2 | a0001 | c0002 | t0008 | g0157 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18983 | hp1 | a0001 | c0002 | t0071 | g0123 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18987 | hp1 | a0001 | c0002 | t0004 | g0327 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18988 | hp2 | a0001 | c0002 | t0072 | g0148 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18989 | hp2 | a0001 | c0001 | t0012 | g0087 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18993 | hp1 | a0001 | c0002 | t0020 | g0333 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0135 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18994 | hp1 | a0001 | c0002 | t0020 | g0332 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0335 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18995 | hp2 | a0001 | c0001 | t0056 | g0132 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18998 | hp1 | a0001 | c0002 | t0008 | g0003 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0338 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA18999 | hp2 | a0001 | c0001 | t0012 | g0134 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19002 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19005 | hp2 | a0001 | c0002 | t0039 | g0318 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19010 | hp1 | a0001 | c0002 | t0073 | g0282 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19010 | hp2 | a0001 | c0001 | t0049 | g0277 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19011 | hp1 | a0001 | c0002 | t0008 | g0174 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19030 | hp1 | a0001 | c0002 | t0010 | g0180 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | LWK | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19062 | hp1 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0336 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19068 | hp1 | a0001 | c0001 | t0023 | g0245 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19070 | hp1 | a0001 | c0002 | t0004 | g0324 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19072 | hp1 | a0003 | c0010 | t0036 | g0341 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19072 | hp2 | a0001 | c0001 | t0012 | g0131 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19075 | hp1 | a0001 | c0001 | t0053 | g0113 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19075 | hp2 | a0001 | c0001 | t0029 | g0307 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19079 | hp2 | a0001 | c0001 | t0026 | g0209 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19085 | hp1 | a0001 | c0002 | t0038 | g0325 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19086 | hp2 | a0001 | c0001 | t0019 | g0328 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19240 | hp1 | a0001 | c0002 | t0057 | g0021 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA19240 | hp2 | a0001 | c0004 | t0011 | g0194 | AFR | YRI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ASW | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | ASW | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20752 | hp1 | a0001 | c0001 | t0033 | g0083 | EUR | TSI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20752 | hp2 | a0001 | c0001 | t0022 | g0116 | EUR | TSI | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0191 | SAS | GIH | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02109 | hp1 | a0001 | c0002 | t0059 | g0005 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02109 | hp2 | a0001 | c0003 | t0009 | g0026 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02486 | hp2 | a0001 | c0001 | t0017 | g0294 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02559 | hp1 | a0001 | c0001 | t0044 | g0207 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG02559 | hp2 | a0001 | c0002 | t0014 | g0075 | AFR | ACB | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03471 | hp1 | a0001 | c0004 | t0011 | g0192 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG03471 | hp2 | a0001 | c0002 | t0062 | g0161 | AFR | MSL | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG06807 | hp1 | a0001 | c0001 | t0030 | g0019 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
HG06807 | hp2 | a0001 | c0002 | t0010 | g0119 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20300 | hp1 | a0001 | c0003 | t0009 | g0025 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | USA | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
homoSapiens | chm13v2 | a0001 | c0002 | t0010 | g0296 | REF | REF | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
homoSapiens | grch38p0 | a0001 | c0001 | t0080 | g0031 | REF | REF | CXADR_chr21_17508043_17575100 | CXADR | chr21 | 17508043 | 17575100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513172 | G | C | 1 | a0004 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant&splice_region_variant | MODERATE | c.43G>C | p.Asp15His | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 130/5593 | 43/1098 | 15/365 | chr21 | 17513172 | |||
chr21:17565507 | A | G | 1 | a0005 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.913A>G | p.Met305Val | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1000/5593 | 913/1098 | 305/365 | chr21 | 17565507 | |||
chr21:17565577 | G | A | 1 | a0003 | 2 | HG02155.hp1 NA19072.hp1 |
missense_variant | MODERATE | c.983G>A | p.Arg328His | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1070/5593 | 983/1098 | 328/365 | chr21 | 17565577 | |||
chr21:17565660 | C | T | 1 | a0002 | 4 | HG02258.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1066C>T | p.Pro356Ser | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1153/5593 | 1066/1098 | 356/365 | chr21 | 17565660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513150 | C | T | 1 | a0001c0013 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.21C>T | p.Phe7Phe | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 108/5593 | 21/1098 | 7/365 | chr21 | 17513150 | |||
chr21:17547103 | A | G | 1 | a0001c0007 | 3 | HG02717.hp1 HG03225.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.120A>G | p.Pro40Pro | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/7 | 207/5593 | 120/1098 | 40/365 | chr21 | 17547103 | |||
chr21:17547148 | C | A | 1 | a0001c0011 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.165C>A | p.Ile55Ile | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/7 | 252/5593 | 165/1098 | 55/365 | chr21 | 17547148 | |||
chr21:17551871 | A | G | 2 | a0001c0003 a0001c0004 |
16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
synonymous_variant | LOW | c.333A>G | p.Gln111Gln | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/7 | 420/5593 | 333/1098 | 111/365 | chr21 | 17551871 | |||
chr21:17560709 | T | A | 1 | a0001c0009 | 2 | HG02976.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.579T>A | p.Thr193Thr | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/7 | 666/5593 | 579/1098 | 193/365 | chr21 | 17560709 | |||
chr21:17565440 | A | G | 5 | a0001c0002 a0001c0004 a0001c0013 others(2): Show |
78 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(75): Show |
synonymous_variant | LOW | c.846A>G | p.Pro282Pro | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 933/5593 | 846/1098 | 282/365 | chr21 | 17565440 | |||
chr21:17565644 | G | A | 1 | a0001c0006 | 3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1050G>A | p.Ala350Ala | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1137/5593 | 1050/1098 | 350/365 | chr21 | 17565644 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513072 | T | C | 11 | a0001c0001t0019 a0001c0002t0004 a0001c0002t0020 others(8): Show |
24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-58T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 58 | chr21 | 17513072 | ||||||
chr21:17513072 | T | G | 1 | a0001c0004t0040 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/7 | 58 | chr21 | 17513072 | ||||||
chr21:17565725 | T | C | 3 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 |
7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*33T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 33 | chr21 | 17565725 | ||||||
chr21:17565762 | G | T | 9 | a0001c0002t0006 a0001c0002t0010 a0001c0002t0014 others(6): Show |
25 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*70G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 70 | chr21 | 17565762 | ||||||
chr21:17565800 | ATAAGT | A | 3 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 |
7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*112_*116delGTTAA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 112 | INFO_REALIGN_3_PRIME | chr21 | 17565800 | |||||
chr21:17565858 | G | A | 27 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(24): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*166G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 166 | chr21 | 17565858 | ||||||
chr21:17565942 | T | G | 48 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(45): Show |
146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 250 | chr21 | 17565942 | ||||||
chr21:17566091 | G | T | 15 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0020 others(12): Show |
34 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*399G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 399 | chr21 | 17566091 | ||||||
chr21:17566167 | C | T | 2 | a0001c0002t0006 a0001c0002t0086 |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*475C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 475 | chr21 | 17566167 | ||||||
chr21:17566297 | A | G | 1 | a0001c0001t0026 | 2 | NA18966.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*605A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 605 | chr21 | 17566297 | ||||||
chr21:17566351 | T | C | 1 | a0001c0002t0027 | 2 | HG01975.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*659T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 659 | chr21 | 17566351 | ||||||
chr21:17566359 | T | C | 31 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(28): Show |
106 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*667T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 667 | chr21 | 17566359 | ||||||
chr21:17566421 | T | C | 14 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0020 others(11): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*729T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 729 | chr21 | 17566421 | ||||||
chr21:17566449 | G | A | 4 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 others(1): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*757G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 757 | chr21 | 17566449 | ||||||
chr21:17566662 | ATGT | A | 14 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0020 others(11): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*981_*983delGTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 981 | INFO_REALIGN_3_PRIME | chr21 | 17566662 | |||||
chr21:17566684 | G | A | 2 | a0001c0009t0074 a0001c0009t0075 |
2 | HG02976.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 992 | chr21 | 17566684 | ||||||
chr21:17566861 | G | C | 1 | a0001c0001t0041 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1169G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1169 | chr21 | 17566861 | ||||||
chr21:17566946 | T | TA | 29 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(26): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1266dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1267 | INFO_REALIGN_3_PRIME | chr21 | 17566946 | |||||
chr21:17566946 | TA | T | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1266delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1266 | INFO_REALIGN_3_PRIME | chr21 | 17566946 | |||||
chr21:17566986 | G | A | 91 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(88): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1294G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1294 | chr21 | 17566986 | ||||||
chr21:17567065 | C | G | 1 | a0001c0001t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1373 | chr21 | 17567065 | ||||||
chr21:17567111 | T | C | 31 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(28): Show |
106 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1419 | chr21 | 17567111 | ||||||
chr21:17567128 | C | T | 14 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(11): Show |
69 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1436C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1436 | chr21 | 17567128 | ||||||
chr21:17567156 | C | G | 2 | a0001c0002t0014 a0001c0002t0085 |
5 | HG00642.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1464C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1464 | chr21 | 17567156 | ||||||
chr21:17567251 | A | G | 1 | a0001c0001t0068 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1559A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1559 | chr21 | 17567251 | ||||||
chr21:17567306 | T | C | 1 | a0001c0002t0020 | 2 | NA18993.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1614T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1614 | chr21 | 17567306 | ||||||
chr21:17567390 | G | A | 2 | a0001c0001t0007 a0001c0001t0042 |
10 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1698 | chr21 | 17567390 | ||||||
chr21:17567511 | C | T | 2 | a0001c0002t0039 a0001c0002t0073 |
2 | NA19005.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1819C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1819 | chr21 | 17567511 | ||||||
chr21:17567621 | A | G | 27 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(24): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1929A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1929 | chr21 | 17567621 | ||||||
chr21:17567638 | T | C | 1 | a0001c0001t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1946T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1946 | chr21 | 17567638 | ||||||
chr21:17567657 | G | A | 4 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 others(1): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1965G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 1965 | chr21 | 17567657 | ||||||
chr21:17567770 | C | T | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2078 | chr21 | 17567770 | ||||||
chr21:17567862 | C | CT | 25 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(22): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2181dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2182 | INFO_REALIGN_3_PRIME | chr21 | 17567862 | |||||
chr21:17567862 | CT | C | 16 | a0001c0001t0028 a0001c0002t0004 a0001c0002t0008 others(13): Show |
36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2181delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2181 | INFO_REALIGN_3_PRIME | chr21 | 17567862 | |||||
chr21:17568012 | T | C | 5 | a0001c0002t0013 a0001c0002t0057 a0001c0002t0059 others(2): Show |
8 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2320T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2320 | chr21 | 17568012 | ||||||
chr21:17568125 | C | CT | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(38): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*2454dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | |||||
chr21:17568125 | C | CTT | 22 | a0001c0001t0025 a0001c0001t0029 a0001c0001t0033 others(19): Show |
50 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2453_*2454dupTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | |||||
chr21:17568125 | C | CTTT | 11 | a0001c0001t0003 a0001c0001t0028 a0001c0001t0051 others(8): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2452_*2454dupTTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2455 | INFO_REALIGN_3_PRIME | chr21 | 17568125 | |||||
chr21:17568161 | G | C | 49 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(46): Show |
147 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*2469G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2469 | chr21 | 17568161 | ||||||
chr21:17568168 | A | G | 35 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(32): Show |
114 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2476A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2476 | chr21 | 17568168 | ||||||
chr21:17568189 | C | T | 1 | a0001c0001t0046 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2497 | chr21 | 17568189 | ||||||
chr21:17568191 | G | C | 2 | a0001c0001t0046 a0001c0001t0047 |
2 | HG01258.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2499G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2499 | chr21 | 17568191 | ||||||
chr21:17568206 | G | T | 31 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(28): Show |
106 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2514G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2514 | chr21 | 17568206 | ||||||
chr21:17568207 | C | T | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2515 | chr21 | 17568207 | ||||||
chr21:17568215 | G | A | 2 | a0001c0001t0022 a0001c0001t0044 |
3 | HG00741.hp1 HG02559.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2523 | chr21 | 17568215 | ||||||
chr21:17568330 | G | A | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2638G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2638 | chr21 | 17568330 | ||||||
chr21:17568379 | C | T | 7 | a0001c0002t0004 a0001c0002t0035 a0001c0002t0037 others(4): Show |
17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2687C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2687 | chr21 | 17568379 | ||||||
chr21:17568406 | G | A | 4 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 others(1): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2714G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2714 | chr21 | 17568406 | ||||||
chr21:17568407 | C | T | 1 | a0001c0001t0049 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2715 | chr21 | 17568407 | ||||||
chr21:17568498 | CTT | C | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2808_*2809delTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2808 | INFO_REALIGN_3_PRIME | chr21 | 17568498 | |||||
chr21:17568529 | A | G | 2 | a0001c0006t0032 a0001c0006t0078 |
3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2837A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2837 | chr21 | 17568529 | ||||||
chr21:17568540 | G | T | 2 | a0001c0001t0031 a0001c0001t0079 |
3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2848G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2848 | chr21 | 17568540 | ||||||
chr21:17568557 | C | CT | 25 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(22): Show |
91 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2882dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2883 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | |||||
chr21:17568557 | C | CTT | 5 | a0001c0001t0067 a0001c0002t0011 a0001c0004t0011 others(2): Show |
9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2881_*2882dupTT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2883 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | |||||
chr21:17568557 | CT | C | 42 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(39): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2882delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2882 | INFO_REALIGN_3_PRIME | chr21 | 17568557 | |||||
chr21:17568566 | T | C | 4 | a0001c0001t0031 a0001c0001t0079 a0002c0005t0018 others(1): Show |
7 | HG02145.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2874 | chr21 | 17568566 | ||||||
chr21:17568582 | A | G | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2890A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2890 | chr21 | 17568582 | ||||||
chr21:17568605 | G | C | 30 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(27): Show |
105 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2913G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2913 | chr21 | 17568605 | ||||||
chr21:17568671 | G | T | 2 | a0001c0001t0012 a0001c0001t0056 |
6 | NA18989.hp2 NA18993.hp2 NA18995.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2979G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 2979 | chr21 | 17568671 | ||||||
chr21:17568743 | G | C | 4 | a0001c0002t0011 a0001c0004t0011 a0001c0004t0040 others(1): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3051 | chr21 | 17568743 | ||||||
chr21:17568769 | G | A | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3077G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3077 | chr21 | 17568769 | ||||||
chr21:17568781 | C | G | 2 | a0001c0002t0027 a0001c0002t0062 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3089C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3089 | chr21 | 17568781 | ||||||
chr21:17568797 | C | G | 9 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0029 others(6): Show |
57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3105C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3105 | chr21 | 17568797 | ||||||
chr21:17568828 | A | G | 1 | a0001c0002t0037 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3136 | chr21 | 17568828 | ||||||
chr21:17568945 | A | G | 18 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(15): Show |
77 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3253A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3253 | chr21 | 17568945 | ||||||
chr21:17569132 | A | G | 1 | a0001c0001t0055 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3440A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3440 | chr21 | 17569132 | ||||||
chr21:17569133 | T | C | 1 | a0001c0002t0070 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3441T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3441 | chr21 | 17569133 | ||||||
chr21:17569366 | T | TTA | 17 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0020 others(14): Show |
36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3686_*3687dupAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3688 | INFO_REALIGN_3_PRIME | chr21 | 17569366 | |||||
chr21:17569366 | TTA | T | 16 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0029 others(13): Show |
68 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3686_*3687delAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3686 | INFO_REALIGN_3_PRIME | chr21 | 17569366 | |||||
chr21:17569383 | C | T | 26 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(23): Show |
101 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3691C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3691 | chr21 | 17569383 | ||||||
chr21:17569397 | A | G | 1 | a0001c0001t0048 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3705A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3705 | chr21 | 17569397 | ||||||
chr21:17569515 | A | G | 1 | a0001c0001t0028 | 2 | HG02055.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3823A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3823 | chr21 | 17569515 | ||||||
chr21:17569657 | G | C | 34 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0028 others(31): Show |
113 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3965G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 3965 | chr21 | 17569657 | ||||||
chr21:17569753 | G | A | 2 | a0001c0001t0028 a0001c0011t0063 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4061G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4061 | chr21 | 17569753 | ||||||
chr21:17569758 | C | T | 2 | a0004c0008t0082 a0004c0008t0084 |
2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4066C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4066 | chr21 | 17569758 | ||||||
chr21:17569787 | T | C | 2 | a0001c0003t0009 a0001c0003t0064 |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4095T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4095 | chr21 | 17569787 | ||||||
chr21:17569870 | G | A | 3 | a0001c0001t0023 a0001c0001t0050 a0001c0001t0055 |
4 | NA18941.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4178G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4178 | chr21 | 17569870 | ||||||
chr21:17569905 | G | A | 28 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(25): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*4213G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4213 | chr21 | 17569905 | ||||||
chr21:17569931 | G | A | 7 | a0001c0002t0011 a0001c0002t0057 a0001c0002t0059 others(4): Show |
11 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4239G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4239 | chr21 | 17569931 | ||||||
chr21:17570025 | C | G | 2 | a0001c0002t0027 a0001c0002t0062 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4333C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 7/7 | 4333 | chr21 | 17570025 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr21:17513186 | A | C | 24 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(21): Show |
24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+14A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513186 | |||||||
chr21:17513228 | C | G | 29 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.43+56C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513228 | |||||||
chr21:17513267 | C | G | 1 | a0003c0010t0036g0341 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.43+95C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513267 | |||||||
chr21:17513356 | C | A | 17 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(14): Show |
17 | HG00423.hp2 HG00609.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.43+184C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513356 | |||||||
chr21:17513408 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+236C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513408 | |||||||
chr21:17513410 | G | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.43+238G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513410 | |||||||
chr21:17513423 | G | A | 1 | a0001c0001t0007g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.43+251G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513423 | |||||||
chr21:17513454 | C | T | 23 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(20): Show |
23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+282C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513454 | |||||||
chr21:17513575 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.43+403T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513575 | |||||||
chr21:17513580 | C | T | 97 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0196 others(94): Show |
99 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.43+408C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513580 | |||||||
chr21:17513624 | T | C | 8 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+452T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513624 | |||||||
chr21:17513642 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+470A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513642 | |||||||
chr21:17513649 | A | G | 3 | a0001c0001t0002g0193 a0001c0004t0011g0192 a0001c0004t0011g0194 |
3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+477A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513649 | |||||||
chr21:17513651 | G | A | 23 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(20): Show |
23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+479G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513651 | |||||||
chr21:17513657 | G | T | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.43+485G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513657 | |||||||
chr21:17513942 | A | C | 1 | a0001c0001t0003g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43+770A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513942 | |||||||
chr21:17513950 | G | C | 1 | a0001c0001t0002g0020 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.43+778G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17513950 | |||||||
chr21:17514192 | C | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+1020C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514192 | |||||||
chr21:17514201 | G | A | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+1029G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514201 | |||||||
chr21:17514208 | T | G | 1 | a0001c0001t0003g0006 | 2 | NA18953.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.43+1036T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514208 | |||||||
chr21:17514447 | G | A | 5 | a0001c0001t0003g0022 a0001c0003t0009g0023 a0001c0003t0009g0024 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1275G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514447 | |||||||
chr21:17514524 | C | T | 3 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 |
3 | HG00323.hp2 NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.43+1352C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514524 | |||||||
chr21:17514565 | GA | G | 238 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(235): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.43+1407delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514565 | ||||||
chr21:17514565 | GAAA | G | 15 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+1405_43+1407del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514565 | ||||||
chr21:17514567 | A | G | 3 | a0001c0001t0002g0193 a0001c0004t0011g0192 a0001c0004t0011g0194 |
3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+1395A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514567 | |||||||
chr21:17514637 | CT | C | 7 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(4): Show |
7 | HG01243.hp1 HG01257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+1479delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514637 | ||||||
chr21:17514685 | G | A | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+1513G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514685 | |||||||
chr21:17514733 | A | G | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0007t0033g0186 others(2): Show |
5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+1561A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514733 | |||||||
chr21:17514739 | T | G | 24 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(21): Show |
24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+1567T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514739 | |||||||
chr21:17514794 | C | T | 2 | a0001c0001t0031g0182 a0001c0001t0031g0183 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.43+1622C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514794 | |||||||
chr21:17514813 | T | C | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+1641T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514813 | |||||||
chr21:17514883 | C | G | 85 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0110 others(82): Show |
88 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.43+1711C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514883 | |||||||
chr21:17514886 | A | T | 8 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+1714A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17514886 | |||||||
chr21:17514973 | A | AT | 14 | a0001c0001t0001g0181 a0001c0001t0002g0017 a0001c0001t0002g0189 others(11): Show |
14 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.43+1813dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17514973 | ||||||
chr21:17515130 | C | A | 2 | a0001c0001t0003g0200 a0001c0001t0029g0199 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.43+1958C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515130 | |||||||
chr21:17515165 | C | T | 85 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0110 others(82): Show |
88 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.43+1993C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515165 | |||||||
chr21:17515283 | A | G | 84 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0110 others(81): Show |
87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.43+2111A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515283 | |||||||
chr21:17515360 | T | A | 256 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.43+2188T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515360 | |||||||
chr21:17515408 | G | A | 16 | a0001c0001t0002g0017 a0001c0001t0002g0107 a0001c0001t0002g0189 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+2236G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515408 | |||||||
chr21:17515432 | A | T | 11 | a0001c0001t0003g0022 a0001c0002t0006g0101 a0001c0002t0011g0105 others(8): Show |
11 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+2260A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515432 | |||||||
chr21:17515447 | C | CA | 16 | a0001c0001t0001g0201 a0001c0001t0002g0017 a0001c0001t0002g0189 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+2286dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17515447 | ||||||
chr21:17515476 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.43+2304T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515476 | |||||||
chr21:17515509 | A | G | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+2337A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515509 | |||||||
chr21:17515559 | C | T | 1 | a0001c0002t0010g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+2387C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515559 | |||||||
chr21:17515602 | G | A | 8 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+2430G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515602 | |||||||
chr21:17515636 | C | A | 6 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(3): Show |
6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2464C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515636 | |||||||
chr21:17515662 | A | T | 1 | a0001c0004t0040g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43+2490A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515662 | |||||||
chr21:17515717 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+2545A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515717 | |||||||
chr21:17515808 | A | C | 24 | a0001c0001t0002g0009 a0001c0001t0002g0092 a0001c0001t0002g0093 others(21): Show |
25 | HG00639.hp1 HG01361.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.43+2636A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17515808 | |||||||
chr21:17516072 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+2900G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516072 | |||||||
chr21:17516162 | C | G | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+2990C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516162 | |||||||
chr21:17516223 | G | A | 6 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(3): Show |
6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+3051G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516223 | |||||||
chr21:17516400 | G | A | 6 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(3): Show |
6 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+3228G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516400 | |||||||
chr21:17516464 | G | T | 14 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.43+3292G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516464 | |||||||
chr21:17516546 | T | C | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+3374T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516546 | |||||||
chr21:17516653 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.43+3481C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17516653 | |||||||
chr21:17516815 | AGT | A | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0196 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.43+3646_43+3647del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17516815 | ||||||
chr21:17516952 | GA | G | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+3788delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17516952 | ||||||
chr21:17517156 | A | G | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+3984A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517156 | |||||||
chr21:17517447 | G | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG02523.hp2 NA18943.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+4275G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517447 | |||||||
chr21:17517553 | G | C | 8 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+4381G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517553 | |||||||
chr21:17517570 | A | G | 3 | a0001c0001t0001g0281 a0001c0002t0039g0318 a0001c0002t0073g0282 |
3 | NA19005.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.43+4398A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517570 | |||||||
chr21:17517666 | C | T | 3 | a0001c0001t0002g0193 a0001c0004t0011g0192 a0001c0004t0011g0194 |
3 | HG02886.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.43+4494C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517666 | |||||||
chr21:17517680 | A | C | 11 | a0001c0001t0003g0022 a0001c0002t0006g0101 a0001c0002t0011g0105 others(8): Show |
11 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+4508A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517680 | |||||||
chr21:17517683 | T | TTGAAGA | 39 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(36): Show |
39 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.43+4516_43+4517ins others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17517683 | ||||||
chr21:17517734 | A | G | 15 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+4562A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517734 | |||||||
chr21:17517741 | A | T | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+4569A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517741 | |||||||
chr21:17517899 | G | A | 14 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.43+4727G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517899 | |||||||
chr21:17517958 | C | T | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+4786C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17517958 | |||||||
chr21:17518043 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+4871C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518043 | |||||||
chr21:17518122 | G | A | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+4950G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518122 | |||||||
chr21:17518141 | G | A | 2 | a0001c0001t0002g0301 a0001c0001t0002g0302 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+4969G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518141 | |||||||
chr21:17518141 | GA | G | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+4970delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518141 | |||||||
chr21:17518170 | G | T | 1 | a0001c0003t0009g0179 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43+4998G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518170 | |||||||
chr21:17518181 | G | A | 6 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+5009G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518181 | |||||||
chr21:17518230 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43+5058A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518230 | |||||||
chr21:17518264 | AC | A | 3 | a0001c0001t0005g0176 a0001c0001t0005g0177 a0001c0001t0017g0175 |
3 | HG01168.hp2 HG01169.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.43+5094delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17518264 | ||||||
chr21:17518266 | C | A | 278 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.43+5094C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518266 | |||||||
chr21:17518308 | A | G | 25 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0001t0068g0029 others(22): Show |
25 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.43+5136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518308 | |||||||
chr21:17518335 | C | G | 3 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0027g0018 |
3 | HG02055.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.43+5163C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518335 | |||||||
chr21:17518560 | A | T | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+5388A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518560 | |||||||
chr21:17518806 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+5634C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518806 | |||||||
chr21:17518892 | A | G | 14 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(11): Show |
intron_variant | MODIFIER | c.43+5720A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518892 | |||||||
chr21:17518908 | T | C | 1 | a0001c0003t0009g0179 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43+5736T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518908 | |||||||
chr21:17518953 | C | T | 1 | a0001c0001t0017g0294 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+5781C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17518953 | |||||||
chr21:17519003 | A | G | 2 | a0001c0002t0020g0332 a0001c0002t0020g0333 |
2 | NA18993.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.43+5831A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519003 | |||||||
chr21:17519024 | C | T | 5 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0280 others(2): Show |
5 | HG02027.hp1 NA18960.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5852C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519024 | |||||||
chr21:17519040 | C | T | 2 | a0001c0001t0002g0301 a0001c0001t0002g0302 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+5868C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519040 | |||||||
chr21:17519063 | G | A | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+5891G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519063 | |||||||
chr21:17519082 | T | G | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+5910T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519082 | |||||||
chr21:17519445 | A | G | 1 | a0001c0001t0003g0027 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.43+6273A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519445 | |||||||
chr21:17519610 | G | C | 1 | a0001c0001t0002g0114 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.43+6438G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519610 | |||||||
chr21:17519634 | C | T | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6462C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519634 | |||||||
chr21:17519691 | T | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | NA19011.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.43+6519T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519691 | |||||||
chr21:17519696 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.43+6524G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519696 | |||||||
chr21:17519707 | T | C | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6535T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519707 | |||||||
chr21:17519734 | G | C | 13 | a0001c0001t0002g0017 a0001c0001t0002g0189 a0001c0001t0002g0190 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+6562G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519734 | |||||||
chr21:17519758 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+6586C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519758 | |||||||
chr21:17519806 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0002g0273 |
2 | HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.43+6634A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519806 | |||||||
chr21:17519976 | T | TAC | 15 | a0001c0001t0002g0009 a0001c0001t0002g0193 a0001c0001t0002g0289 others(12): Show |
16 | HG01361.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.43+6819_43+6820dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17519976 | ||||||
chr21:17519993 | G | A | 1 | a0001c0002t0006g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.43+6821G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519993 | |||||||
chr21:17519996 | C | T | 1 | a0001c0002t0008g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.43+6824C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17519996 | |||||||
chr21:17520041 | C | A | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+6869C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520041 | |||||||
chr21:17520346 | G | A | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0196 others(105): Show |
110 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.43+7174G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520346 | |||||||
chr21:17520407 | T | C | 84 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0110 others(81): Show |
87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.43+7235T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520407 | |||||||
chr21:17520586 | A | T | 1 | a0001c0001t0001g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.43+7414A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520586 | |||||||
chr21:17520648 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(221): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.43+7476G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520648 | |||||||
chr21:17520779 | T | C | 20 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0001c0001t0001g0312 others(17): Show |
20 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+7607T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520779 | |||||||
chr21:17520802 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+7630C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520802 | |||||||
chr21:17520843 | A | G | 23 | a0001c0001t0019g0320 a0001c0001t0019g0328 a0001c0002t0004g0319 others(20): Show |
23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+7671A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520843 | |||||||
chr21:17520844 | T | C | 1 | a0001c0001t0046g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+7672T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520844 | |||||||
chr21:17520898 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0043g0117 |
2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.43+7726G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17520898 | |||||||
chr21:17521022 | T | G | 8 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(5): Show |
8 | HG01243.hp1 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+7850T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521022 | |||||||
chr21:17521053 | A | G | 332 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(329): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.43+7881A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521053 | |||||||
chr21:17521083 | T | C | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0007t0033g0186 others(2): Show |
5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+7911T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521083 | |||||||
chr21:17521117 | A | T | 1 | a0001c0001t0002g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43+7945A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521117 | |||||||
chr21:17521131 | A | G | 15 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0006g0101 others(12): Show |
15 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+7959A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521131 | |||||||
chr21:17521179 | G | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+8007G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521179 | |||||||
chr21:17521280 | G | A | 2 | a0001c0002t0010g0119 a0001c0002t0010g0180 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.43+8108G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521280 | |||||||
chr21:17521300 | G | A | 1 | a0001c0002t0004g0319 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.43+8128G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521300 | |||||||
chr21:17521318 | TTTA | T | 17 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0107 others(14): Show |
18 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.43+8164_43+8166del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521318 | ||||||
chr21:17521345 | C | T | 6 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+8173C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521345 | |||||||
chr21:17521375 | T | A | 183 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(180): Show |
187 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.43+8203T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521375 | |||||||
chr21:17521464 | A | G | 12 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(9): Show |
12 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+8292A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521464 | |||||||
chr21:17521537 | G | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+8365G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521537 | |||||||
chr21:17521548 | C | CCTGA | 3 | a0001c0002t0057g0021 a0001c0003t0016g0184 a0001c0004t0011g0185 |
3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.43+8378_43+8381dup others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521548 | ||||||
chr21:17521559 | GTGA | G | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+8389_43+8391del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17521559 | ||||||
chr21:17521694 | G | A | 1 | a0001c0002t0027g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.43+8522G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17521694 | |||||||
chr21:17522133 | G | C | 128 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(125): Show |
132 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.43+8961G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522133 | |||||||
chr21:17522154 | C | CT | 11 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(8): Show |
12 | HG02683.hp2 HG02717.hp1 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+8992dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17522154 | ||||||
chr21:17522164 | T | G | 1 | a0001c0002t0004g0321 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.43+8992T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522164 | |||||||
chr21:17522195 | C | T | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+9023C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522195 | |||||||
chr21:17522197 | A | G | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+9025A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522197 | |||||||
chr21:17522198 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.43+9026G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522198 | |||||||
chr21:17522200 | G | T | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+9028G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522200 | |||||||
chr21:17522209 | C | T | 9 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(6): Show |
9 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+9037C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522209 | |||||||
chr21:17522315 | AT | A | 57 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0020 others(54): Show |
60 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.43+9147delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17522315 | ||||||
chr21:17522335 | C | T | 2 | a0001c0001t0003g0300 a0001c0002t0006g0299 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.43+9163C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522335 | |||||||
chr21:17522347 | C | T | 1 | a0001c0001t0005g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43+9175C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522347 | |||||||
chr21:17522348 | A | G | 89 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(86): Show |
93 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.43+9176A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522348 | |||||||
chr21:17522360 | C | G | 40 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+9188C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522360 | |||||||
chr21:17522375 | C | T | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+9203C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522375 | |||||||
chr21:17522391 | G | A | 22 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(19): Show |
22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+9219G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522391 | |||||||
chr21:17522480 | A | G | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+9308A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522480 | |||||||
chr21:17522693 | T | C | 1 | a0001c0001t0028g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43+9521T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522693 | |||||||
chr21:17522909 | T | C | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+9737T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522909 | |||||||
chr21:17522958 | A | G | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+9786A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522958 | |||||||
chr21:17522974 | T | C | 1 | a0001c0001t0051g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.43+9802T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17522974 | |||||||
chr21:17523049 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0042g0270 |
2 | HG00099.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.43+9877A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523049 | |||||||
chr21:17523406 | C | G | 3 | a0001c0002t0021g0330 a0001c0002t0021g0331 a0001c0002t0034g0329 |
3 | HG02015.hp2 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.43+10234C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523406 | |||||||
chr21:17523491 | C | G | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+10319C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523491 | |||||||
chr21:17523542 | CAT | C | 6 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10372_43+10373d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17523542 | ||||||
chr21:17523579 | G | A | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+10407G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523579 | |||||||
chr21:17523652 | T | A | 9 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+10480T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523652 | |||||||
chr21:17523670 | A | T | 1 | a0001c0004t0011g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43+10498A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523670 | |||||||
chr21:17523753 | G | A | 180 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(177): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.43+10581G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523753 | |||||||
chr21:17523894 | T | C | 39 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(36): Show |
39 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.43+10722T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523894 | |||||||
chr21:17523928 | G | A | 92 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(89): Show |
96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.43+10756G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17523928 | |||||||
chr21:17524003 | C | T | 5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0007t0033g0186 others(2): Show |
5 | HG02976.hp2 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+10831C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524003 | |||||||
chr21:17524028 | T | TTG | 11 | a0001c0001t0001g0269 a0001c0002t0004g0334 a0001c0002t0004g0335 others(8): Show |
11 | HG00673.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+10869_43+10870d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524028 | ||||||
chr21:17524041 | T | TGTGC | 4 | a0001c0001t0002g0193 a0001c0001t0017g0294 a0001c0004t0011g0192 others(1): Show |
4 | HG02486.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+10870_43+10871i others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524041 | ||||||
chr21:17524043 | C | CGT | 89 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0002g0004 others(86): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.43+10894_43+10895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524043 | ||||||
chr21:17524043 | C | T | 4 | a0001c0001t0002g0193 a0001c0001t0017g0294 a0001c0004t0011g0192 others(1): Show |
4 | HG02486.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+10871C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524043 | |||||||
chr21:17524043 | CGT | C | 5 | a0001c0001t0079g0077 a0001c0002t0014g0074 a0001c0002t0014g0075 others(2): Show |
5 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+10894_43+10895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524043 | ||||||
chr21:17524090 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.43+10918C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524090 | |||||||
chr21:17524172 | G | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0272 a0001c0001t0003g0006 others(1): Show |
5 | NA18948.hp2 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+11000G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524172 | |||||||
chr21:17524195 | A | T | 60 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0020 others(57): Show |
63 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.43+11023A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524195 | |||||||
chr21:17524219 | C | T | 3 | a0001c0002t0057g0021 a0001c0003t0016g0184 a0001c0004t0011g0185 |
3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.43+11047C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524219 | |||||||
chr21:17524240 | C | T | 2 | a0001c0003t0009g0025 a0001c0003t0009g0026 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.43+11068C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524240 | |||||||
chr21:17524347 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.43+11175A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524347 | |||||||
chr21:17524427 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.43+11255T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524427 | |||||||
chr21:17524490 | C | T | 59 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0020 others(56): Show |
62 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.43+11318C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524490 | |||||||
chr21:17524575 | C | CA | 17 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0315 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+11430dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CA | C | 33 | a0001c0001t0001g0043 a0001c0001t0003g0022 a0001c0001t0003g0045 others(30): Show |
33 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+11430delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CAA | C | 66 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0066 others(63): Show |
68 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.43+11429_43+11430d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CAAA | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0108 others(115): Show |
120 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.43+11428_43+11430d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CAAAAAA | C | 72 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0017 others(69): Show |
76 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.43+11425_43+11430d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0198 a0001c0001t0015g0265 |
2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.43+11421_43+11430d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524575 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+11418_43+11430d others(15): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17524575 | ||||||
chr21:17524765 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43+11593C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524765 | |||||||
chr21:17524779 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+11607C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17524779 | |||||||
chr21:17525079 | T | C | 1 | a0001c0001t0055g0305 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.43+11907T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525079 | |||||||
chr21:17525205 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0002g0212 |
2 | HG02132.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.43+12033T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525205 | |||||||
chr21:17525244 | G | A | 1 | a0001c0001t0001g0288 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.43+12072G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525244 | |||||||
chr21:17525358 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.43+12186A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525358 | |||||||
chr21:17525369 | A | C | 1 | a0001c0001t0028g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+12197A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525369 | |||||||
chr21:17525474 | C | T | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+12302C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525474 | |||||||
chr21:17525608 | T | A | 92 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(89): Show |
96 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.43+12436T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525608 | |||||||
chr21:17525725 | A | G | 7 | a0001c0002t0004g0334 a0001c0002t0004g0335 a0001c0002t0004g0336 others(4): Show |
7 | HG00673.hp2 HG02074.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+12553A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525725 | |||||||
chr21:17525759 | T | C | 1 | a0001c0001t0017g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.43+12587T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525759 | |||||||
chr21:17525909 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.43+12737A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17525909 | |||||||
chr21:17526014 | T | C | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+12842T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526014 | |||||||
chr21:17526045 | A | C | 1 | a0001c0004t0011g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43+12873A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526045 | |||||||
chr21:17526054 | C | T | 22 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(19): Show |
22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+12882C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526054 | |||||||
chr21:17526279 | T | C | 61 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0002g0004 others(58): Show |
64 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.43+13107T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526279 | |||||||
chr21:17526364 | A | T | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+13192A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526364 | |||||||
chr21:17526508 | G | A | 1 | a0001c0001t0003g0213 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.43+13336G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526508 | |||||||
chr21:17526577 | G | T | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+13405G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526577 | |||||||
chr21:17526583 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+13411G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526583 | |||||||
chr21:17526831 | G | GTTTTGT | 6 | a0001c0001t0067g0015 a0001c0002t0061g0016 a0001c0002t0062g0161 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+13675_43+13680d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17526831 | ||||||
chr21:17526911 | A | C | 9 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+13739A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17526911 | |||||||
chr21:17527093 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+13921T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527093 | |||||||
chr21:17527174 | G | A | 8 | a0001c0001t0079g0077 a0001c0002t0010g0119 a0001c0002t0010g0180 others(5): Show |
8 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+14002G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527174 | |||||||
chr21:17527194 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+14022G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527194 | |||||||
chr21:17527285 | A | C | 2 | a0001c0003t0016g0184 a0001c0004t0011g0185 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.43+14113A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527285 | |||||||
chr21:17527372 | G | A | 22 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(19): Show |
22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+14200G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527372 | |||||||
chr21:17527385 | C | T | 6 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+14213C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527385 | |||||||
chr21:17527509 | G | T | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+14337G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527509 | |||||||
chr21:17527653 | T | C | 2 | a0001c0001t0007g0214 a0001c0001t0007g0215 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.43+14481T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527653 | |||||||
chr21:17527681 | G | A | 1 | a0001c0002t0037g0323 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43+14509G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527681 | |||||||
chr21:17527688 | C | G | 1 | a0001c0004t0011g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.43+14516C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527688 | |||||||
chr21:17527726 | C | A | 40 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+14554C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527726 | |||||||
chr21:17527800 | T | TTTTA | 10 | a0001c0001t0002g0193 a0001c0001t0005g0160 a0001c0001t0017g0294 others(7): Show |
12 | HG01099.hp1 HG01192.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.43+14648_43+14651d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17527800 | ||||||
chr21:17527820 | A | T | 1 | a0001c0001t0047g0262 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.43+14648A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527820 | |||||||
chr21:17527842 | C | T | 40 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+14670C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527842 | |||||||
chr21:17527932 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+14760C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527932 | |||||||
chr21:17527957 | A | G | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+14785A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17527957 | |||||||
chr21:17528060 | A | C | 1 | a0001c0002t0027g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.43+14888A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528060 | |||||||
chr21:17528068 | C | CT | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0110 others(111): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.43+14919dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | ||||||
chr21:17528068 | C | CTT | 22 | a0001c0001t0001g0108 a0001c0001t0001g0137 a0001c0001t0001g0138 others(19): Show |
22 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+14918_43+14919d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | ||||||
chr21:17528068 | CT | C | 47 | a0001c0001t0002g0017 a0001c0001t0002g0081 a0001c0001t0002g0092 others(44): Show |
47 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.43+14919delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | ||||||
chr21:17528068 | CTT | C | 91 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(88): Show |
95 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.43+14918_43+14919d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | ||||||
chr21:17528068 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.43+14910_43+14919d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17528068 | ||||||
chr21:17528071 | T | G | 8 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0001t0067g0015 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+14899T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528071 | |||||||
chr21:17528072 | T | G | 1 | a0001c0006t0078g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.43+14900T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528072 | |||||||
chr21:17528073 | T | C | 11 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(8): Show |
11 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+14901T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528073 | |||||||
chr21:17528074 | T | C | 20 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(17): Show |
20 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+14902T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528074 | |||||||
chr21:17528075 | T | C | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+14903T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528075 | |||||||
chr21:17528100 | G | T | 1 | a0001c0001t0002g0317 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43+14928G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528100 | |||||||
chr21:17528265 | G | A | 24 | a0001c0001t0003g0022 a0001c0001t0019g0328 a0001c0002t0004g0319 others(21): Show |
24 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.43+15093G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528265 | |||||||
chr21:17528363 | C | T | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+15191C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528363 | |||||||
chr21:17528709 | A | G | 1 | a0001c0001t0046g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+15537A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528709 | |||||||
chr21:17528832 | T | C | 333 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.43+15660T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528832 | |||||||
chr21:17528852 | C | T | 23 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(20): Show |
23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+15680C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528852 | |||||||
chr21:17528938 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.43+15766C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528938 | |||||||
chr21:17528965 | G | A | 2 | a0001c0001t0002g0301 a0001c0001t0002g0302 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.43+15793G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17528965 | |||||||
chr21:17529034 | C | CT | 31 | a0001c0001t0001g0111 a0001c0001t0001g0260 a0001c0001t0001g0280 others(28): Show |
31 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.43+15884dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | ||||||
chr21:17529034 | CT | C | 25 | a0001c0001t0001g0053 a0001c0001t0001g0206 a0001c0001t0001g0218 others(22): Show |
25 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.43+15884delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | ||||||
chr21:17529034 | CTTTTTTT others(5): Show |
C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0002g0004 others(91): Show |
98 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.43+15873_43+15884d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | ||||||
chr21:17529034 | CTTTTTTT others(7): Show |
C | 22 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(19): Show |
22 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.43+15871_43+15884d others(16): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529034 | ||||||
chr21:17529100 | G | A | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+15928G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529100 | |||||||
chr21:17529252 | C | T | 4 | a0001c0001t0031g0182 a0001c0001t0031g0183 a0001c0007t0002g0090 others(1): Show |
4 | HG02717.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+16080C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529252 | |||||||
chr21:17529266 | C | T | 1 | a0001c0003t0009g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.43+16094C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529266 | |||||||
chr21:17529315 | G | C | 40 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.43+16143G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529315 | |||||||
chr21:17529502 | A | G | 179 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(176): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.43+16330A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529502 | |||||||
chr21:17529651 | G | A | 126 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0009 others(123): Show |
130 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.43+16479G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529651 | |||||||
chr21:17529774 | C | A | 333 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.43+16602C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529774 | |||||||
chr21:17529795 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+16623T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529795 | |||||||
chr21:17529922 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.43+16750T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529922 | |||||||
chr21:17529931 | ATTTTTC | A | 23 | a0001c0001t0019g0328 a0001c0002t0004g0319 a0001c0002t0004g0321 others(20): Show |
23 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.43+16777_43+16782d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17529931 | ||||||
chr21:17529955 | T | C | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+16783T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529955 | |||||||
chr21:17529970 | A | G | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43+16798A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17529970 | |||||||
chr21:17530028 | A | G | 1 | a0001c0004t0011g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+16856A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530028 | |||||||
chr21:17530051 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.43+16879C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530051 | |||||||
chr21:17530059 | T | C | 333 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.43+16887T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530059 | |||||||
chr21:17530114 | A | AT | 102 | a0001c0001t0001g0011 a0001c0001t0001g0311 a0001c0001t0001g0315 others(99): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.44-16895dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530114 | A | ATT | 13 | a0001c0001t0001g0312 a0001c0001t0002g0301 a0001c0001t0002g0302 others(10): Show |
13 | HG01175.hp1 HG01175.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16896_44-16895d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530114 | A | ATTT | 57 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(54): Show |
59 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.44-16897_44-16895d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530114 | A | ATTTT | 21 | a0001c0001t0001g0066 a0001c0001t0001g0110 a0001c0001t0001g0221 others(18): Show |
21 | HG01109.hp1 HG01261.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.44-16898_44-16895d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530114 | A | ATTTTT | 104 | a0001c0001t0001g0007 a0001c0001t0001g0108 a0001c0001t0001g0111 others(101): Show |
106 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.44-16899_44-16895d others(7): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530114 | A | ATTTTTT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0210 others(18): Show |
21 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.44-16900_44-16895d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530114 | ||||||
chr21:17530205 | A | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG02132.hp2 HG02135.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-16822A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530205 | |||||||
chr21:17530220 | C | T | 13 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(10): Show |
13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16807C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530220 | |||||||
chr21:17530224 | C | G | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-16803C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530224 | |||||||
chr21:17530294 | AT | A | 9 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(6): Show |
9 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-16730delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17530294 | ||||||
chr21:17530453 | G | C | 13 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(10): Show |
13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-16574G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530453 | |||||||
chr21:17530551 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.44-16476C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530551 | |||||||
chr21:17530641 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-16386C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530641 | |||||||
chr21:17530755 | G | A | 61 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0020 others(58): Show |
64 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.44-16272G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530755 | |||||||
chr21:17530762 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0003t0009g0023 others(4): Show |
7 | HG01109.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-16265C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530762 | |||||||
chr21:17530766 | A | G | 1 | a0001c0001t0079g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.44-16261A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530766 | |||||||
chr21:17530792 | C | T | 4 | a0001c0002t0008g0157 a0001c0002t0008g0158 a0001c0002t0008g0174 others(1): Show |
4 | HG02056.hp2 NA18981.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-16235C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530792 | |||||||
chr21:17530820 | A | C | 10 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0057g0021 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-16207A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530820 | |||||||
chr21:17530892 | T | A | 2 | a0001c0001t0002g0301 a0001c0001t0002g0302 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.44-16135T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17530892 | |||||||
chr21:17531038 | G | A | 6 | a0001c0001t0079g0077 a0001c0002t0014g0074 a0001c0002t0014g0075 others(3): Show |
6 | HG00642.hp1 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-15989G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531038 | |||||||
chr21:17531109 | C | G | 1 | a0001c0001t0002g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.44-15918C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531109 | |||||||
chr21:17531118 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.44-15909C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531118 | |||||||
chr21:17531146 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-15881A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531146 | |||||||
chr21:17531162 | G | A | 3 | a0001c0001t0022g0116 a0001c0001t0022g0259 a0001c0001t0044g0207 |
3 | HG00741.hp1 HG02559.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.44-15865G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531162 | |||||||
chr21:17531164 | G | A | 3 | a0001c0003t0009g0151 a0001c0003t0009g0179 a0001c0003t0064g0145 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-15863G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531164 | |||||||
chr21:17531170 | G | A | 1 | a0001c0001t0046g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.44-15857G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531170 | |||||||
chr21:17531214 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.44-15813G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531214 | |||||||
chr21:17531229 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.44-15798G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531229 | |||||||
chr21:17531277 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.44-15750C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531277 | |||||||
chr21:17531298 | C | CA | 6 | a0001c0001t0002g0009 a0001c0001t0002g0289 a0001c0001t0002g0290 others(3): Show |
7 | HG02683.hp2 HG03491.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-15716dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | ||||||
chr21:17531298 | CA | C | 110 | a0001c0001t0001g0011 a0001c0001t0002g0004 a0001c0001t0002g0017 others(107): Show |
113 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.44-15716delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | ||||||
chr21:17531298 | CAA | C | 13 | a0001c0001t0003g0297 a0001c0001t0003g0298 a0001c0001t0003g0300 others(10): Show |
13 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-15717_44-15716d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531298 | ||||||
chr21:17531319 | A | G | 3 | a0001c0002t0057g0021 a0001c0003t0016g0184 a0001c0004t0011g0185 |
3 | HG01243.hp1 HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.44-15708A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531319 | |||||||
chr21:17531339 | T | G | 40 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0060 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.44-15688T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531339 | |||||||
chr21:17531347 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-15680C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531347 | |||||||
chr21:17531415 | A | G | 11 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0002t0010g0180 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-15612A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531415 | |||||||
chr21:17531438 | T | C | 41 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0288 others(38): Show |
43 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-15589T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531438 | |||||||
chr21:17531536 | A | G | 331 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(328): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.44-15491A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531536 | |||||||
chr21:17531555 | G | C | 1 | a0001c0001t0003g0213 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.44-15472G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531555 | |||||||
chr21:17531573 | C | T | 3 | a0001c0001t0002g0098 a0001c0002t0006g0099 a0001c0002t0006g0100 |
3 | HG00639.hp1 HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.44-15454C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531573 | |||||||
chr21:17531721 | A | G | 3 | a0001c0002t0006g0001 a0001c0002t0006g0115 a0001c0002t0086g0001 |
5 | HG01099.hp1 HG01192.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-15306A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531721 | |||||||
chr21:17531779 | CTT | C | 25 | a0001c0001t0002g0098 a0001c0001t0002g0193 a0001c0001t0005g0160 others(22): Show |
27 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.44-15244_44-15243d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531779 | ||||||
chr21:17531786 | G | C | 1 | a0001c0001t0022g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.44-15241G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531786 | |||||||
chr21:17531937 | G | GT | 185 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(182): Show |
189 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.44-15076dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531937 | ||||||
chr21:17531937 | G | GTT | 42 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0288 others(39): Show |
43 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.44-15077_44-15076d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17531937 | ||||||
chr21:17531998 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44-15029G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17531998 | |||||||
chr21:17532008 | C | T | 2 | a0001c0001t0003g0063 a0001c0001t0003g0070 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.44-15019C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532008 | |||||||
chr21:17532009 | A | C | 2 | a0001c0001t0003g0063 a0001c0001t0003g0070 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.44-15018A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532009 | |||||||
chr21:17532042 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0206 a0001c0001t0001g0218 others(2): Show |
5 | HG02040.hp2 HG02155.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-14985C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532042 | |||||||
chr21:17532183 | C | T | 256 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(253): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.44-14844C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532183 | |||||||
chr21:17532196 | G | C | 3 | a0001c0006t0032g0013 a0001c0006t0032g0014 a0001c0006t0078g0012 |
3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.44-14831G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532196 | |||||||
chr21:17532261 | G | C | 10 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(7): Show |
10 | HG00639.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-14766G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532261 | |||||||
chr21:17532309 | G | A | 5 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0006t0032g0013 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14718G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532309 | |||||||
chr21:17532339 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0017g0294 |
2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.44-14688A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532339 | |||||||
chr21:17532402 | ACTGT | A | 16 | a0001c0001t0002g0017 a0001c0001t0005g0032 a0001c0001t0005g0033 others(13): Show |
16 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.44-14622_44-14619d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17532402 | ||||||
chr21:17532432 | A | G | 3 | a0001c0002t0057g0021 a0001c0002t0059g0005 a0001c0002t0060g0005 |
3 | HG02109.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-14595A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532432 | |||||||
chr21:17532445 | A | C | 2 | a0001c0002t0020g0332 a0001c0002t0020g0333 |
2 | NA18993.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.44-14582A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532445 | |||||||
chr21:17532474 | C | T | 181 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.44-14553C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532474 | |||||||
chr21:17532507 | AG | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(109): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.44-14519delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532507 | |||||||
chr21:17532508 | G | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-14519G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532508 | |||||||
chr21:17532636 | GGCACTGC others(5): Show |
G | 34 | a0001c0001t0003g0139 a0001c0001t0003g0169 a0001c0002t0004g0319 others(31): Show |
35 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.44-14388_44-14377d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17532636 | ||||||
chr21:17532770 | G | A | 1 | a0001c0001t0046g0203 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.44-14257G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532770 | |||||||
chr21:17532785 | T | C | 1 | a0001c0002t0010g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44-14242T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17532785 | |||||||
chr21:17533041 | G | A | 10 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(7): Show |
12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-13986G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533041 | |||||||
chr21:17533080 | T | A | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-13947T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533080 | |||||||
chr21:17533153 | A | T | 1 | a0001c0001t0017g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-13874A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533153 | |||||||
chr21:17533581 | G | A | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-13446G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533581 | |||||||
chr21:17533587 | A | G | 16 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(13): Show |
18 | HG00639.hp1 HG00642.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-13440A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533587 | |||||||
chr21:17533631 | G | T | 1 | a0001c0001t0003g0266 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44-13396G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533631 | |||||||
chr21:17533712 | A | G | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-13315A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533712 | |||||||
chr21:17533824 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0025g0249 a0001c0001t0026g0209 others(1): Show |
4 | HG00423.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-13203C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533824 | |||||||
chr21:17533873 | G | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.44-13154G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533873 | |||||||
chr21:17533900 | T | C | 1 | a0001c0001t0017g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-13127T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17533900 | |||||||
chr21:17534007 | A | AAT | 7 | a0001c0001t0002g0098 a0001c0001t0002g0212 a0001c0001t0005g0039 others(4): Show |
7 | HG02258.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-13000_44-12999d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | ||||||
chr21:17534007 | A | AATATAT | 15 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(12): Show |
15 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-13004_44-12999d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | ||||||
chr21:17534007 | AAT | A | 99 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0118 others(96): Show |
104 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.44-13000_44-12999d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | ||||||
chr21:17534007 | AATAT | A | 7 | a0001c0004t0011g0041 a0001c0004t0011g0079 a0001c0004t0011g0185 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-13002_44-12999d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534007 | ||||||
chr21:17534012 | ATATATAT others(11): Show |
A | 4 | a0001c0002t0014g0075 a0001c0002t0014g0076 a0001c0002t0014g0078 others(1): Show |
4 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-12998_44-12981d others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534012 | ||||||
chr21:17534019 | T | TATATAGC others(17): Show |
1 | a0001c0003t0016g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.44-13003_44-13002i others(26): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | ||||||
chr21:17534019 | T | TATATAGC others(19): Show |
1 | a0001c0001t0001g0111 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.44-13003_44-13002i others(28): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | ||||||
chr21:17534019 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0198 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.44-13001_44-13000i others(28): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | ||||||
chr21:17534019 | T | TATATATA others(21): Show |
107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.44-13001_44-13000i others(30): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | ||||||
chr21:17534019 | T | TATATATA others(53): Show |
1 | a0001c0001t0015g0251 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.44-13001_44-13000i others(62): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534019 | ||||||
chr21:17534027 | T | G | 30 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0008g0003 others(27): Show |
31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-13000T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534027 | |||||||
chr21:17534028 | A | C | 30 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0008g0003 others(27): Show |
31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12999A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534028 | |||||||
chr21:17534029 | G | T | 30 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0008g0003 others(27): Show |
31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12998G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534029 | |||||||
chr21:17534030 | C | A | 30 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0008g0003 others(27): Show |
31 | HG01109.hp2 HG02015.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.44-12997C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534030 | |||||||
chr21:17534030 | C | CTA | 21 | a0001c0001t0002g0172 a0001c0001t0002g0317 a0001c0002t0004g0319 others(18): Show |
21 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.44-12982_44-12981d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534030 | ||||||
chr21:17534030 | CTA | C | 74 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(71): Show |
76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.44-12982_44-12981d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534030 | ||||||
chr21:17534032 | A | ATATATAT others(15): Show |
1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12981_44-12980i others(24): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534032 | ||||||
chr21:17534045 | T | C | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-12982T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534045 | |||||||
chr21:17534060 | C | CTA | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(118): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.44-12958_44-12957d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | ||||||
chr21:17534060 | C | CTATATAT others(23): Show |
2 | a0001c0001t0001g0288 a0001c0001t0007g0314 |
2 | HG00099.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(32): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | ||||||
chr21:17534060 | C | CTATATAT others(25): Show |
2 | a0001c0001t0001g0011 a0001c0001t0019g0328 |
2 | HG01928.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(34): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | ||||||
chr21:17534060 | C | CTATATAT others(51): Show |
1 | a0001c0001t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.44-12957_44-12956i others(60): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | ||||||
chr21:17534060 | C | CTATATAT others(27): Show |
3 | a0001c0001t0001g0118 a0001c0001t0043g0117 a0001c0009t0075g0187 |
3 | HG01074.hp1 HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.44-12957_44-12956i others(36): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534060 | ||||||
chr21:17534069 | T | TATAC | 17 | a0001c0001t0001g0110 a0001c0001t0001g0231 a0001c0001t0001g0242 others(14): Show |
19 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-12957_44-12956i others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534069 | ||||||
chr21:17534069 | T | TATATACA others(27): Show |
1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.44-12957_44-12956i others(36): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534069 | ||||||
chr21:17534071 | C | T | 141 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0197 others(138): Show |
145 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.44-12956C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534071 | |||||||
chr21:17534073 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.44-12954C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534073 | |||||||
chr21:17534079 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.44-12948C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534079 | |||||||
chr21:17534081 | C | CATATAT | 3 | a0001c0001t0002g0222 a0001c0002t0008g0157 a0001c0003t0009g0023 |
3 | HG03041.hp1 NA18522.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.44-12931_44-12926d others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | ||||||
chr21:17534081 | C | T | 14 | a0001c0001t0001g0060 a0001c0001t0001g0110 a0001c0001t0001g0136 others(11): Show |
14 | HG00099.hp2 HG00323.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-12946C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534081 | |||||||
chr21:17534081 | CAT | C | 27 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0109 others(24): Show |
28 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.44-12927_44-12926d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | ||||||
chr21:17534081 | CATAT | C | 3 | a0002c0005t0018g0143 a0002c0005t0018g0150 a0002c0005t0018g0152 |
3 | HG02258.hp2 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.44-12929_44-12926d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534081 | ||||||
chr21:17534083 | T | C | 13 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0197 others(10): Show |
13 | HG01069.hp1 HG01517.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-12944T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534083 | |||||||
chr21:17534085 | T | C | 3 | a0001c0001t0031g0182 a0001c0001t0031g0183 a0001c0001t0079g0077 |
3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-12942T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534085 | |||||||
chr21:17534098 | A | AT | 9 | a0001c0001t0003g0085 a0001c0001t0003g0140 a0001c0001t0003g0170 others(6): Show |
9 | HG00597.hp2 HG02165.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.44-12928dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534098 | ||||||
chr21:17534098 | A | T | 9 | a0001c0001t0003g0022 a0001c0001t0003g0046 a0001c0001t0003g0059 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-12929A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534098 | |||||||
chr21:17534098 | ATAT | A | 6 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG00323.hp2 HG01069.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-12927_44-12925d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534098 | ||||||
chr21:17534099 | TA | T | 4 | a0001c0001t0002g0168 a0001c0001t0003g0027 a0001c0001t0003g0050 others(1): Show |
4 | HG00609.hp2 HG01433.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-12927delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534099 | |||||||
chr21:17534100 | A | AT | 6 | a0001c0002t0010g0119 a0001c0002t0010g0180 a0001c0002t0014g0074 others(3): Show |
6 | HG00642.hp1 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-12902dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATATATAT | 6 | a0001c0002t0008g0042 a0001c0002t0008g0158 a0001c0002t0008g0174 others(3): Show |
6 | HG02027.hp2 HG02056.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(9): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATATATAT others(2): Show |
9 | a0001c0002t0004g0334 a0001c0002t0004g0335 a0001c0002t0004g0336 others(6): Show |
9 | HG00673.hp2 HG02074.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATATATTT others(2): Show |
8 | a0001c0002t0004g0322 a0001c0002t0004g0324 a0001c0002t0004g0327 others(5): Show |
8 | HG00423.hp2 HG02155.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATATATTT others(4): Show |
1 | a0001c0002t0004g0321 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.44-12926_44-12925i others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATATATTT others(5): Show |
1 | a0001c0002t0004g0319 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.44-12926_44-12925i others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | ATTT | 11 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0002t0006g0001 others(8): Show |
12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-12904_44-12902d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534100 | A | T | 52 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(49): Show |
53 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.44-12927A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534100 | |||||||
chr21:17534100 | AT | A | 8 | a0001c0001t0005g0176 a0001c0002t0010g0225 a0001c0002t0010g0308 others(5): Show |
8 | HG01074.hp2 HG01169.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-12902delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534100 | ||||||
chr21:17534101 | T | TA | 29 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0138 others(26): Show |
29 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-12926_44-12925i others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534101 | |||||||
chr21:17534101 | T | TATA | 3 | a0001c0001t0001g0181 a0001c0001t0007g0232 a0001c0002t0061g0016 |
3 | HG02735.hp1 HG02735.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.44-12926_44-12925i others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534101 | |||||||
chr21:17534102 | T | A | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(105): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.44-12925T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534102 | |||||||
chr21:17534103 | T | A | 23 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0138 others(20): Show |
23 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.44-12924T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534103 | |||||||
chr21:17534104 | T | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.44-12923T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534104 | |||||||
chr21:17534105 | T | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0210 others(11): Show |
14 | HG00673.hp1 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.44-12922T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534105 | |||||||
chr21:17534106 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0118 others(6): Show |
10 | HG00735.hp1 HG01074.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12921T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534106 | |||||||
chr21:17534107 | T | A | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12920T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534107 | |||||||
chr21:17534110 | T | A | 2 | a0001c0001t0028g0089 a0001c0011t0063g0159 |
2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-12917T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534110 | |||||||
chr21:17534211 | G | A | 94 | a0001c0001t0002g0017 a0001c0001t0003g0002 a0001c0001t0003g0006 others(91): Show |
98 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.44-12816G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534211 | |||||||
chr21:17534215 | C | T | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12812C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534215 | |||||||
chr21:17534257 | C | T | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-12770C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534257 | |||||||
chr21:17534258 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-12769G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534258 | |||||||
chr21:17534278 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0219 others(5): Show |
8 | HG00558.hp1 HG02083.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-12749G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534278 | |||||||
chr21:17534571 | G | T | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-12456G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534571 | |||||||
chr21:17534583 | G | C | 13 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0003t0009g0023 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-12444G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534583 | |||||||
chr21:17534767 | A | ATTTGTCT others(3): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0268 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.44-12257_44-12248d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534767 | ||||||
chr21:17534787 | T | G | 1 | a0001c0013t0010g0295 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44-12240T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534787 | |||||||
chr21:17534789 | C | CT | 119 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0043 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.44-12224dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534789 | C | CTTTTTTT others(2): Show |
11 | a0001c0001t0003g0046 a0001c0002t0006g0001 a0001c0002t0006g0099 others(8): Show |
13 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-12232_44-12224d others(11): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534789 | C | CTTTTTTT others(3): Show |
70 | a0001c0001t0002g0017 a0001c0001t0003g0002 a0001c0001t0003g0006 others(67): Show |
72 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.44-12233_44-12224d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534789 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0003g0049 a0001c0001t0028g0089 a0001c0002t0010g0180 others(4): Show |
7 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-12234_44-12224d others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534789 | C | CTTTTTTT others(5): Show |
30 | a0001c0001t0003g0030 a0001c0001t0028g0088 a0001c0002t0004g0319 others(27): Show |
31 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.44-12235_44-12224d others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534789 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0008g0047 a0003c0010t0036g0341 |
2 | HG04184.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.44-12236_44-12224d others(15): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17534789 | ||||||
chr21:17534859 | A | C | 1 | a0001c0001t0012g0135 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.44-12168A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534859 | |||||||
chr21:17534941 | C | T | 3 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 |
3 | HG00323.hp2 NA18954.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.44-12086C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17534941 | |||||||
chr21:17535304 | T | G | 19 | a0001c0001t0003g0030 a0001c0002t0004g0319 a0001c0002t0004g0321 others(16): Show |
19 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-11723T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535304 | |||||||
chr21:17535506 | A | G | 5 | a0001c0001t0003g0139 a0001c0001t0003g0169 a0001c0001t0003g0170 others(2): Show |
5 | HG00597.hp2 HG02083.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-11521A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535506 | |||||||
chr21:17535658 | T | C | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-11369T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535658 | |||||||
chr21:17535659 | A | C | 13 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0003t0009g0023 others(10): Show |
13 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-11368A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535659 | |||||||
chr21:17535756 | C | T | 2 | a0001c0001t0003g0195 a0001c0001t0003g0226 |
2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.44-11271C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535756 | |||||||
chr21:17535968 | A | G | 6 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-11059A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17535968 | |||||||
chr21:17536013 | T | A | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-11014T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536013 | |||||||
chr21:17536076 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0136 |
3 | HG00735.hp1 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.44-10951C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536076 | |||||||
chr21:17536110 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.44-10917T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536110 | |||||||
chr21:17536149 | A | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-10878A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536149 | |||||||
chr21:17536186 | A | C | 141 | a0001c0001t0001g0060 a0001c0001t0002g0017 a0001c0001t0003g0002 others(138): Show |
146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-10841A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536186 | |||||||
chr21:17536187 | C | T | 1 | a0001c0002t0027g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-10840C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536187 | |||||||
chr21:17536232 | A | G | 9 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(6): Show |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-10795A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536232 | |||||||
chr21:17536260 | T | C | 8 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-10767T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536260 | |||||||
chr21:17536312 | A | G | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-10715A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536312 | |||||||
chr21:17536392 | C | T | 2 | a0004c0008t0082g0309 a0004c0008t0084g0310 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.44-10635C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536392 | |||||||
chr21:17536403 | G | A | 1 | a0001c0001t0068g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.44-10624G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536403 | |||||||
chr21:17536503 | C | A | 140 | a0001c0001t0002g0017 a0001c0001t0003g0002 a0001c0001t0003g0006 others(137): Show |
145 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.44-10524C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536503 | |||||||
chr21:17536742 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.44-10285A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536742 | |||||||
chr21:17536949 | G | A | 9 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(6): Show |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-10078G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536949 | |||||||
chr21:17536995 | T | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-10032T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17536995 | |||||||
chr21:17537018 | A | G | 1 | a0001c0001t0081g0162 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.44-10009A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537018 | |||||||
chr21:17537055 | A | G | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-9972A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537055 | |||||||
chr21:17537105 | T | C | 2 | a0001c0002t0014g0076 a0001c0002t0085g0073 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.44-9922T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537105 | |||||||
chr21:17537118 | A | G | 11 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(8): Show |
11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-9909A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537118 | |||||||
chr21:17537437 | T | C | 1 | a0001c0002t0027g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.44-9590T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537437 | |||||||
chr21:17537554 | G | A | 2 | a0001c0002t0027g0018 a0001c0002t0027g0142 |
2 | HG01975.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.44-9473G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537554 | |||||||
chr21:17537623 | A | G | 5 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0006t0032g0013 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-9404A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537623 | |||||||
chr21:17537722 | A | C | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-9305A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537722 | |||||||
chr21:17537725 | A | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-9302A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537725 | |||||||
chr21:17537728 | A | G | 141 | a0001c0001t0001g0060 a0001c0001t0002g0017 a0001c0001t0003g0002 others(138): Show |
146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-9299A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537728 | |||||||
chr21:17537761 | CT | C | 4 | a0001c0002t0004g0334 a0001c0002t0004g0335 a0001c0002t0004g0336 others(1): Show |
4 | HG00673.hp2 NA18967.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-9265delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537761 | |||||||
chr21:17537880 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.44-9147C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537880 | |||||||
chr21:17537903 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0030g0019 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.44-9124T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17537903 | |||||||
chr21:17538184 | A | G | 2 | a0001c0001t0005g0037 a0001c0001t0005g0038 |
2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.44-8843A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538184 | |||||||
chr21:17538189 | T | C | 141 | a0001c0001t0001g0060 a0001c0001t0002g0017 a0001c0001t0003g0002 others(138): Show |
146 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.44-8838T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538189 | |||||||
chr21:17538199 | C | G | 8 | a0001c0003t0016g0184 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-8828C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538199 | |||||||
chr21:17538200 | C | T | 1 | a0001c0001t0015g0265 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-8827C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538200 | |||||||
chr21:17538201 | G | A | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-8826G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538201 | |||||||
chr21:17538262 | A | G | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-8765A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538262 | |||||||
chr21:17538285 | C | G | 4 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0001t0003g0297 others(1): Show |
4 | HG01109.hp1 HG01361.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-8742C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538285 | |||||||
chr21:17538341 | G | T | 6 | a0001c0001t0001g0198 a0001c0001t0001g0288 a0001c0001t0015g0265 others(3): Show |
6 | HG00423.hp1 HG01257.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-8686G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538341 | |||||||
chr21:17538396 | G | A | 1 | a0001c0001t0066g0054 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.44-8631G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538396 | |||||||
chr21:17538470 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44-8557C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538470 | |||||||
chr21:17538594 | C | T | 2 | a0002c0005t0018g0150 a0002c0005t0018g0152 |
2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.44-8433C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538594 | |||||||
chr21:17538644 | G | A | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-8383G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538644 | |||||||
chr21:17538680 | G | C | 1 | a0001c0001t0016g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44-8347G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538680 | |||||||
chr21:17538702 | G | A | 3 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0135 |
3 | NA18993.hp2 NA19062.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.44-8325G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17538702 | |||||||
chr21:17539026 | C | T | 11 | a0001c0001t0001g0206 a0001c0001t0001g0218 a0001c0001t0001g0221 others(8): Show |
11 | HG02040.hp2 HG02080.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-8001C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539026 | |||||||
chr21:17539027 | G | A | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-8000G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539027 | |||||||
chr21:17539175 | A | G | 1 | a0001c0001t0022g0116 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-7852A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539175 | |||||||
chr21:17539325 | CCAGCTTT others(16): Show |
C | 1 | a0001c0001t0022g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.44-7701_44-7679del others(23): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539325 | |||||||
chr21:17539342 | G | A | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7685G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539342 | |||||||
chr21:17539395 | C | T | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7632C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539395 | |||||||
chr21:17539409 | G | A | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.44-7618G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539409 | |||||||
chr21:17539503 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-7524A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539503 | |||||||
chr21:17539518 | G | C | 1 | a0001c0001t0003g0306 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.44-7509G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539518 | |||||||
chr21:17539637 | T | C | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7390T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539637 | |||||||
chr21:17539800 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.44-7227C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539800 | |||||||
chr21:17539807 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7220C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539807 | |||||||
chr21:17539808 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7219C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539808 | |||||||
chr21:17539882 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.44-7145C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539882 | |||||||
chr21:17539884 | A | G | 3 | a0001c0001t0031g0182 a0001c0001t0031g0183 a0001c0001t0079g0077 |
3 | HG02145.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-7143A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539884 | |||||||
chr21:17539918 | G | GT | 6 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-7108dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17539918 | ||||||
chr21:17539930 | T | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-7097T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539930 | |||||||
chr21:17539939 | C | T | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-7088C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17539939 | |||||||
chr21:17540062 | G | A | 2 | a0001c0002t0021g0330 a0001c0002t0034g0329 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.44-6965G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540062 | |||||||
chr21:17540110 | C | T | 1 | a0001c0004t0011g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.44-6917C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540110 | |||||||
chr21:17540140 | C | T | 1 | a0001c0001t0068g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.44-6887C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540140 | |||||||
chr21:17540178 | G | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0302 a0001c0001t0017g0294 |
3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.44-6849G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540178 | |||||||
chr21:17540309 | C | T | 1 | a0001c0001t0007g0314 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.44-6718C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540309 | |||||||
chr21:17540310 | G | A | 1 | a0001c0001t0017g0294 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-6717G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540310 | |||||||
chr21:17540312 | C | A | 1 | a0002c0005t0018g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-6715C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540312 | |||||||
chr21:17540338 | A | C | 1 | a0002c0005t0018g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-6689A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540338 | |||||||
chr21:17540356 | A | T | 3 | a0001c0002t0057g0021 a0001c0002t0059g0005 a0001c0002t0060g0005 |
3 | HG02109.hp1 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-6671A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540356 | |||||||
chr21:17540358 | T | G | 1 | a0001c0001t0001g0267 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.44-6669T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540358 | |||||||
chr21:17540393 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44-6634A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540393 | |||||||
chr21:17540400 | T | C | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-6627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540400 | |||||||
chr21:17540407 | AT | A | 3 | a0001c0001t0024g0208 a0001c0001t0024g0254 a0001c0001t0045g0261 |
3 | HG00639.hp2 HG01361.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.44-6618delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17540407 | ||||||
chr21:17540490 | G | A | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-6537G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540490 | |||||||
chr21:17540764 | G | C | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-6263G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540764 | |||||||
chr21:17540894 | C | T | 54 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(51): Show |
56 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.44-6133C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540894 | |||||||
chr21:17540985 | G | A | 1 | a0001c0002t0008g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.44-6042G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17540985 | |||||||
chr21:17541026 | C | G | 1 | a0001c0004t0069g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44-6001C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541026 | |||||||
chr21:17541077 | G | A | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-5950G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541077 | |||||||
chr21:17541234 | A | C | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-5793A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541234 | |||||||
chr21:17541248 | C | G | 1 | a0001c0001t0003g0141 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.44-5779C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541248 | |||||||
chr21:17541278 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.44-5749C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541278 | |||||||
chr21:17541358 | C | T | 11 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(8): Show |
11 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-5669C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541358 | |||||||
chr21:17541372 | G | A | 18 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(15): Show |
18 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-5655G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541372 | |||||||
chr21:17541379 | C | T | 1 | a0001c0002t0027g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-5648C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541379 | |||||||
chr21:17541380 | G | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5647G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541380 | |||||||
chr21:17541396 | C | CA | 10 | a0001c0001t0001g0280 a0001c0002t0006g0001 a0001c0002t0006g0099 others(7): Show |
12 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-5620dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541396 | ||||||
chr21:17541474 | C | T | 2 | a0001c0001t0028g0088 a0001c0001t0028g0089 |
2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.44-5553C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541474 | |||||||
chr21:17541499 | A | G | 67 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(64): Show |
69 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-5528A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541499 | |||||||
chr21:17541521 | A | G | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-5506A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541521 | |||||||
chr21:17541596 | C | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5431C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541596 | |||||||
chr21:17541617 | A | AT | 24 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0324 others(21): Show |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.44-5393dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | ||||||
chr21:17541617 | A | ATT | 14 | a0001c0002t0004g0322 a0001c0002t0004g0334 a0001c0002t0008g0003 others(11): Show |
15 | HG00423.hp2 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-5394_44-5393dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | ||||||
chr21:17541617 | AT | A | 267 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(264): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.44-5393delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17541617 | ||||||
chr21:17541774 | G | C | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-5253G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541774 | |||||||
chr21:17541863 | A | G | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.44-5164A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541863 | |||||||
chr21:17541903 | C | A | 4 | a0001c0002t0014g0075 a0001c0002t0014g0076 a0001c0002t0014g0078 others(1): Show |
4 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5124C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541903 | |||||||
chr21:17541916 | T | C | 3 | a0001c0001t0024g0208 a0001c0001t0024g0254 a0001c0001t0045g0261 |
3 | HG00639.hp2 HG01361.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.44-5111T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17541916 | |||||||
chr21:17542001 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.44-5026A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542001 | |||||||
chr21:17542024 | ACT | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-5000_44-4999del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17542024 | ||||||
chr21:17542052 | T | A | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-4975T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542052 | |||||||
chr21:17542068 | A | G | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-4959A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542068 | |||||||
chr21:17542147 | A | G | 4 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0222 others(1): Show |
4 | HG03041.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4880A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542147 | |||||||
chr21:17542168 | TA | T | 7 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(4): Show |
8 | HG02027.hp2 HG02056.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-4858delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542168 | |||||||
chr21:17542249 | A | G | 3 | a0001c0003t0009g0151 a0001c0003t0009g0179 a0001c0003t0064g0145 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-4778A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542249 | |||||||
chr21:17542315 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.44-4712C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542315 | |||||||
chr21:17542614 | G | A | 4 | a0001c0001t0023g0238 a0001c0001t0023g0245 a0001c0001t0050g0216 others(1): Show |
4 | NA18941.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4413G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542614 | |||||||
chr21:17542655 | T | C | 2 | a0001c0001t0001g0264 a0001c0001t0051g0204 |
2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.44-4372T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542655 | |||||||
chr21:17542693 | C | T | 1 | a0001c0002t0008g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.44-4334C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542693 | |||||||
chr21:17542741 | A | G | 12 | a0001c0001t0002g0193 a0001c0001t0002g0302 a0001c0001t0005g0160 others(9): Show |
12 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-4286A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542741 | |||||||
chr21:17542870 | C | G | 73 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(70): Show |
75 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.44-4157C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542870 | |||||||
chr21:17542900 | G | A | 117 | a0001c0001t0002g0193 a0001c0001t0002g0302 a0001c0001t0003g0002 others(114): Show |
120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.44-4127G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542900 | |||||||
chr21:17542918 | G | A | 6 | a0001c0001t0002g0017 a0001c0001t0017g0294 a0001c0001t0030g0019 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-4109G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17542918 | |||||||
chr21:17543000 | A | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-4027A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543000 | |||||||
chr21:17543019 | T | C | 7 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0222 others(4): Show |
7 | HG02717.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4008T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543019 | |||||||
chr21:17543035 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.44-3992G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543035 | |||||||
chr21:17543097 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.44-3930A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543097 | |||||||
chr21:17543114 | G | A | 1 | a0001c0001t0012g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.44-3913G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543114 | |||||||
chr21:17543157 | A | G | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-3870A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543157 | |||||||
chr21:17543312 | C | T | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-3715C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543312 | |||||||
chr21:17543411 | A | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-3616A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543411 | |||||||
chr21:17543494 | C | T | 76 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0020 others(73): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.44-3533C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543494 | |||||||
chr21:17543620 | C | T | 1 | a0001c0003t0016g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.44-3407C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543620 | |||||||
chr21:17543820 | G | A | 12 | a0001c0001t0002g0017 a0001c0001t0005g0160 a0001c0001t0030g0019 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44-3207G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543820 | |||||||
chr21:17543983 | G | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
11 | HG00597.hp1 HG01258.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-3044G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17543983 | |||||||
chr21:17544223 | C | G | 2 | a0001c0009t0074g0188 a0001c0009t0075g0187 |
2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2804C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544223 | |||||||
chr21:17544295 | A | G | 35 | a0001c0001t0001g0011 a0001c0001t0001g0223 a0001c0001t0001g0260 others(32): Show |
36 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.44-2732A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544295 | |||||||
chr21:17544301 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.44-2726A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544301 | |||||||
chr21:17544436 | C | T | 1 | a0001c0001t0017g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-2591C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544436 | |||||||
chr21:17544438 | T | A | 2 | a0001c0002t0027g0018 a0001c0002t0027g0142 |
2 | HG01975.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.44-2589T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544438 | |||||||
chr21:17544467 | G | C | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-2560G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544467 | |||||||
chr21:17544521 | GCTGCAGA others(13): Show |
G | 56 | a0001c0001t0002g0017 a0001c0001t0003g0002 a0001c0001t0003g0006 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.44-2503_44-2484del others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17544521 | ||||||
chr21:17544541 | A | C | 9 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 others(6): Show |
9 | HG01975.hp1 HG02109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-2486A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544541 | |||||||
chr21:17544714 | A | G | 73 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(70): Show |
75 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.44-2313A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544714 | |||||||
chr21:17544744 | T | C | 2 | a0001c0009t0074g0188 a0001c0009t0075g0187 |
2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2283T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544744 | |||||||
chr21:17544764 | A | T | 1 | a0001c0001t0017g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-2263A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544764 | |||||||
chr21:17544780 | C | T | 10 | a0001c0001t0005g0160 a0001c0001t0033g0083 a0001c0002t0011g0105 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-2247C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544780 | |||||||
chr21:17544804 | C | T | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-2223C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544804 | |||||||
chr21:17544865 | A | G | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-2162A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17544865 | |||||||
chr21:17544962 | CCT | C | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-2062_44-2061del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17544962 | ||||||
chr21:17545007 | C | T | 65 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(62): Show |
67 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.44-2020C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545007 | |||||||
chr21:17545072 | G | GT | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0060 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.44-1930dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | G | GTT | 33 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0053 others(30): Show |
33 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.44-1931_44-1930dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | GT | G | 27 | a0001c0001t0002g0020 a0001c0001t0002g0080 a0001c0001t0002g0084 others(24): Show |
27 | HG00423.hp2 HG00621.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.44-1930delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | GTT | G | 86 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0081 others(83): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.44-1931_44-1930del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | GTTT | G | 6 | a0001c0001t0003g0085 a0001c0001t0003g0298 a0001c0001t0005g0035 others(3): Show |
6 | HG01169.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-1932_44-1930del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | GTTTT | G | 14 | a0001c0001t0003g0022 a0001c0001t0003g0057 a0001c0001t0003g0058 others(11): Show |
14 | HG01109.hp1 HG01361.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-1933_44-1930del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545072 | GTTTTT | G | 52 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0027 others(49): Show |
54 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.44-1934_44-1930del others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545072 | ||||||
chr21:17545391 | T | A | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-1636T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545391 | |||||||
chr21:17545400 | T | C | 4 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0001t0003g0297 others(1): Show |
4 | HG01109.hp1 HG01361.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-1627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545400 | |||||||
chr21:17545613 | G | T | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | NA19062.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.44-1414G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545613 | |||||||
chr21:17545666 | G | A | 7 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0222 others(4): Show |
7 | HG02717.hp1 HG03041.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-1361G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545666 | |||||||
chr21:17545771 | G | GTT | 63 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(60): Show |
65 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.44-1256_44-1255ins others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545771 | |||||||
chr21:17545772 | G | T | 74 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(71): Show |
76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.44-1255G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545772 | |||||||
chr21:17545781 | G | GT | 9 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0154 others(6): Show |
10 | HG02683.hp2 HG03098.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-1231dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545781 | ||||||
chr21:17545781 | G | T | 3 | a0001c0001t0003g0050 a0001c0001t0003g0139 a0001c0001t0016g0048 |
3 | HG02738.hp2 HG03688.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.44-1246G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545781 | |||||||
chr21:17545781 | GT | G | 143 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.44-1231delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 17545781 | ||||||
chr21:17545784 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.44-1243T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545784 | |||||||
chr21:17545820 | C | T | 6 | a0001c0001t0001g0236 a0001c0001t0007g0010 a0001c0001t0007g0230 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-1207C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545820 | |||||||
chr21:17545937 | A | G | 6 | a0001c0004t0011g0041 a0001c0004t0011g0079 a0001c0004t0011g0185 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-1090A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545937 | |||||||
chr21:17545951 | G | C | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-1076G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17545951 | |||||||
chr21:17546034 | C | T | 1 | a0001c0001t0016g0048 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.44-993C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546034 | |||||||
chr21:17546068 | C | T | 4 | a0001c0004t0011g0041 a0001c0004t0011g0185 a0001c0004t0011g0194 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-959C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546068 | |||||||
chr21:17546111 | G | A | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.44-916G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546111 | |||||||
chr21:17546126 | G | T | 1 | a0001c0001t0003g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.44-901G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546126 | |||||||
chr21:17546258 | A | G | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-769A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546258 | |||||||
chr21:17546260 | C | A | 56 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0080 others(53): Show |
57 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.44-767C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546260 | |||||||
chr21:17546260 | C | T | 192 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.44-767C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546260 | |||||||
chr21:17546306 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.44-721T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546306 | |||||||
chr21:17546322 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.44-705T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546322 | |||||||
chr21:17546358 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-669C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546358 | |||||||
chr21:17546408 | G | A | 193 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.44-619G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546408 | |||||||
chr21:17546665 | T | C | 2 | a0001c0007t0002g0090 a0001c0007t0002g0091 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.44-362T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546665 | |||||||
chr21:17546672 | G | A | 1 | a0001c0007t0033g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-355G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546672 | |||||||
chr21:17546736 | C | G | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-291C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546736 | |||||||
chr21:17546737 | T | G | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-290T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546737 | |||||||
chr21:17546936 | A | G | 2 | a0001c0003t0009g0023 a0001c0003t0009g0086 |
2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.44-91A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546936 | |||||||
chr21:17546940 | A | G | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.44-87A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546940 | |||||||
chr21:17546962 | C | T | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-65C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 1/6 | chr21 | 17546962 | |||||||
chr21:17547236 | A | T | 1 | a0003c0010t0004g0340 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.210+43A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547236 | |||||||
chr21:17547257 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210+64C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547257 | |||||||
chr21:17547364 | G | A | 2 | a0001c0007t0002g0090 a0001c0007t0002g0091 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.210+171G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547364 | |||||||
chr21:17547434 | G | A | 8 | a0001c0003t0016g0184 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+241G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547434 | |||||||
chr21:17547534 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.210+341C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547534 | |||||||
chr21:17547617 | G | A | 2 | a0001c0002t0004g0319 a0001c0002t0004g0321 |
2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.210+424G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547617 | |||||||
chr21:17547762 | A | AT | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.210+577dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17547762 | ||||||
chr21:17547895 | T | G | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210+702T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547895 | |||||||
chr21:17547937 | C | G | 58 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(55): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.210+744C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17547937 | |||||||
chr21:17548085 | A | C | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+892A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548085 | |||||||
chr21:17548112 | A | G | 13 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(10): Show |
13 | HG01884.hp2 HG01975.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.210+919A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548112 | |||||||
chr21:17548319 | T | C | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1126T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548319 | |||||||
chr21:17548350 | C | A | 1 | a0001c0002t0008g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.210+1157C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548350 | |||||||
chr21:17548368 | C | G | 16 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(13): Show |
16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.210+1175C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548368 | |||||||
chr21:17548373 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.210+1180C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548373 | |||||||
chr21:17548514 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.210+1321T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548514 | |||||||
chr21:17548613 | G | A | 17 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(14): Show |
17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.210+1420G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548613 | |||||||
chr21:17548616 | C | T | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210+1423C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548616 | |||||||
chr21:17548664 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.210+1471G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548664 | |||||||
chr21:17548746 | A | G | 1 | a0001c0001t0019g0320 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.210+1553A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17548746 | |||||||
chr21:17549030 | G | C | 1 | a0001c0001t0002g0084 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.210+1837G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549030 | |||||||
chr21:17549075 | T | A | 1 | a0001c0001t0017g0175 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.210+1882T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549075 | |||||||
chr21:17549262 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+2069C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549262 | |||||||
chr21:17549420 | C | A | 16 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(13): Show |
16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.210+2227C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549420 | |||||||
chr21:17549503 | G | T | 45 | a0001c0001t0005g0160 a0001c0002t0004g0319 a0001c0002t0004g0321 others(42): Show |
46 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.211-2246G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549503 | |||||||
chr21:17549736 | C | G | 1 | a0001c0002t0006g0100 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.211-2013C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549736 | |||||||
chr21:17549737 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.211-2012C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549737 | |||||||
chr21:17549861 | A | G | 2 | a0004c0008t0082g0309 a0004c0008t0084g0310 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.211-1888A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549861 | |||||||
chr21:17549944 | C | T | 8 | a0001c0003t0016g0184 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1805C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17549944 | |||||||
chr21:17550016 | A | G | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1733A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550016 | |||||||
chr21:17550036 | A | T | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211-1713A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550036 | |||||||
chr21:17550043 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.211-1706A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550043 | |||||||
chr21:17550085 | G | A | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.211-1664G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550085 | |||||||
chr21:17550109 | C | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1640C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550109 | |||||||
chr21:17550135 | T | C | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1614T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550135 | |||||||
chr21:17550216 | T | C | 16 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(13): Show |
16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-1533T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550216 | |||||||
chr21:17550280 | G | T | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211-1469G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550280 | |||||||
chr21:17550351 | C | CA | 115 | a0001c0001t0001g0060 a0001c0001t0002g0017 a0001c0001t0003g0002 others(112): Show |
120 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.211-1382dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | ||||||
chr21:17550351 | C | CAA | 192 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.211-1383_211-1382d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | ||||||
chr21:17550351 | C | CAAA | 10 | a0001c0001t0002g0009 a0001c0001t0002g0080 a0001c0001t0002g0082 others(7): Show |
11 | HG00639.hp2 HG01099.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-1384_211-1382d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17550351 | ||||||
chr21:17550370 | T | G | 2 | a0001c0009t0074g0188 a0001c0009t0075g0187 |
2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.211-1379T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550370 | |||||||
chr21:17550377 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.211-1372T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550377 | |||||||
chr21:17550381 | T | G | 1 | a0001c0004t0069g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.211-1368T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550381 | |||||||
chr21:17550454 | C | T | 8 | a0001c0003t0016g0184 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1295C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550454 | |||||||
chr21:17550613 | A | G | 58 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(55): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.211-1136A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550613 | |||||||
chr21:17550664 | T | C | 1 | a0001c0003t0016g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-1085T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550664 | |||||||
chr21:17550795 | G | T | 1 | a0003c0010t0004g0340 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.211-954G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17550795 | |||||||
chr21:17551097 | T | TA | 10 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0193 others(7): Show |
10 | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-651dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 17551097 | ||||||
chr21:17551142 | A | G | 1 | a0001c0003t0009g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-607A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551142 | |||||||
chr21:17551186 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.211-563G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551186 | |||||||
chr21:17551308 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.211-441G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551308 | |||||||
chr21:17551331 | T | C | 16 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(13): Show |
16 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-418T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551331 | |||||||
chr21:17551392 | CAAAAA | C | 8 | a0001c0003t0016g0184 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-356_211-352del others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551392 | |||||||
chr21:17551424 | C | T | 1 | a0001c0004t0040g0316 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.211-325C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551424 | |||||||
chr21:17551547 | A | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-202A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551547 | |||||||
chr21:17551702 | T | G | 9 | a0001c0001t0003g0052 a0001c0003t0009g0023 a0001c0003t0009g0024 others(6): Show |
9 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.211-47T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551702 | |||||||
chr21:17551710 | G | T | 1 | a0001c0002t0008g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.211-39G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 2/6 | chr21 | 17551710 | |||||||
chr21:17552019 | T | C | 10 | a0001c0001t0005g0160 a0001c0002t0011g0105 a0001c0002t0013g0102 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.415+66T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552019 | |||||||
chr21:17552245 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0168 |
2 | HG00438.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.415+292G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552245 | |||||||
chr21:17552383 | A | C | 21 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(18): Show |
21 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.415+430A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552383 | |||||||
chr21:17552385 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0052g0044 |
2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.415+432A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552385 | |||||||
chr21:17552436 | A | G | 2 | a0001c0001t0002g0302 a0001c0001t0017g0294 |
2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.415+483A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552436 | |||||||
chr21:17552481 | T | G | 208 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.415+528T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552481 | |||||||
chr21:17552573 | T | TTA | 9 | a0001c0002t0011g0105 a0001c0003t0016g0184 a0001c0004t0011g0041 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.415+621_415+622dup others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17552573 | ||||||
chr21:17552741 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0043 others(125): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.415+788G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552741 | |||||||
chr21:17552955 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.415+1002C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552955 | |||||||
chr21:17552956 | T | A | 16 | a0001c0002t0011g0105 a0001c0003t0009g0023 a0001c0003t0009g0024 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+1003T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17552956 | |||||||
chr21:17553007 | C | T | 16 | a0001c0002t0011g0105 a0001c0003t0009g0023 a0001c0003t0009g0024 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+1054C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553007 | |||||||
chr21:17553033 | T | C | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1080T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553033 | |||||||
chr21:17553036 | C | T | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1083C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553036 | |||||||
chr21:17553048 | A | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1095A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553048 | |||||||
chr21:17553054 | C | T | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1101C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553054 | |||||||
chr21:17553066 | GCA | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1114_415+1115d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553066 | |||||||
chr21:17553071 | C | CCT | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1118_415+1119i others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553071 | |||||||
chr21:17553072 | A | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1119A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553072 | |||||||
chr21:17553081 | C | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1128C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553081 | |||||||
chr21:17553174 | C | T | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.415+1221C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553174 | |||||||
chr21:17553184 | G | A | 266 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(263): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.415+1231G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553184 | |||||||
chr21:17553223 | G | A | 9 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(6): Show |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+1270G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553223 | |||||||
chr21:17553391 | T | C | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.415+1438T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553391 | |||||||
chr21:17553494 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.415+1541A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553494 | |||||||
chr21:17553531 | G | A | 1 | a0001c0001t0068g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.415+1578G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553531 | |||||||
chr21:17553605 | G | C | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1652G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553605 | |||||||
chr21:17553614 | C | CT | 6 | a0001c0002t0008g0157 a0001c0003t0009g0023 a0001c0003t0009g0026 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1680dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | ||||||
chr21:17553614 | CT | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.415+1680delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | ||||||
chr21:17553614 | CTT | C | 57 | a0001c0001t0001g0060 a0001c0001t0001g0311 a0001c0001t0002g0017 others(54): Show |
59 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.415+1679_415+1680d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | ||||||
chr21:17553614 | CTTT | C | 79 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0020 others(76): Show |
81 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.415+1678_415+1680d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | ||||||
chr21:17553614 | CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1670_415+1680d others(13): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17553614 | ||||||
chr21:17553652 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0025g0249 a0001c0001t0026g0209 others(1): Show |
4 | HG00423.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+1699C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17553652 | |||||||
chr21:17554023 | T | C | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415+2070T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554023 | |||||||
chr21:17554116 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.415+2163C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554116 | |||||||
chr21:17554152 | G | T | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.415+2199G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554152 | |||||||
chr21:17554263 | T | C | 16 | a0001c0002t0011g0105 a0001c0003t0009g0023 a0001c0003t0009g0024 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+2310T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554263 | |||||||
chr21:17554291 | AG | A | 187 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.415+2342delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554291 | ||||||
chr21:17554335 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+2382C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554335 | |||||||
chr21:17554425 | A | G | 1 | a0001c0002t0010g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.415+2472A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554425 | |||||||
chr21:17554445 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.415+2492T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554445 | |||||||
chr21:17554488 | G | C | 16 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(13): Show |
17 | HG00544.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.415+2535G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554488 | |||||||
chr21:17554491 | G | C | 55 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(52): Show |
57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.415+2538G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554491 | |||||||
chr21:17554492 | G | C | 61 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0193 others(58): Show |
62 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.415+2539G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554492 | |||||||
chr21:17554543 | C | T | 43 | a0001c0001t0001g0223 a0001c0001t0005g0160 a0001c0002t0004g0319 others(40): Show |
44 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.415+2590C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554543 | |||||||
chr21:17554567 | A | G | 150 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.415+2614A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554567 | |||||||
chr21:17554616 | T | C | 62 | a0001c0001t0002g0017 a0001c0001t0005g0160 a0001c0001t0030g0019 others(59): Show |
63 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.415+2663T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17554616 | |||||||
chr21:17554819 | TTGAC | T | 16 | a0001c0002t0011g0105 a0001c0003t0009g0023 a0001c0003t0009g0024 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+2870_415+2873d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554819 | ||||||
chr21:17554902 | TG | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+2951delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17554902 | ||||||
chr21:17555085 | A | G | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.415+3132A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555085 | |||||||
chr21:17555300 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0229 a0001c0001t0001g0275 |
3 | HG00735.hp2 HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.415+3347T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555300 | |||||||
chr21:17555421 | A | G | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.415+3468A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555421 | |||||||
chr21:17555515 | C | T | 16 | a0001c0002t0011g0105 a0001c0003t0009g0023 a0001c0003t0009g0024 others(13): Show |
16 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.416-3461C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555515 | |||||||
chr21:17555598 | A | G | 49 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(46): Show |
50 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.416-3378A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555598 | |||||||
chr21:17555625 | T | C | 5 | a0001c0001t0002g0017 a0001c0001t0030g0019 a0001c0006t0032g0013 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3351T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555625 | |||||||
chr21:17555632 | TCTC | T | 23 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(20): Show |
25 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-3339_416-3337d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17555632 | ||||||
chr21:17555658 | A | G | 9 | a0001c0001t0005g0160 a0001c0002t0013g0102 a0001c0002t0013g0103 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-3318A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555658 | |||||||
chr21:17555794 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.416-3182A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555794 | |||||||
chr21:17555831 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.416-3145G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555831 | |||||||
chr21:17555970 | C | T | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-3006C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17555970 | |||||||
chr21:17556052 | A | G | 48 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0027 others(45): Show |
50 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.416-2924A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556052 | |||||||
chr21:17556326 | A | G | 40 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(37): Show |
41 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.416-2650A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556326 | |||||||
chr21:17556414 | T | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.416-2562T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556414 | |||||||
chr21:17556432 | G | A | 302 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(299): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.416-2544G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556432 | |||||||
chr21:17556468 | GA | G | 55 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(52): Show |
57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.416-2504delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17556468 | ||||||
chr21:17556741 | T | A | 55 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(52): Show |
57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.416-2235T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556741 | |||||||
chr21:17556761 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.416-2215G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556761 | |||||||
chr21:17556778 | A | T | 250 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.416-2198A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556778 | |||||||
chr21:17556806 | G | A | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.416-2170G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556806 | |||||||
chr21:17556841 | A | G | 129 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0017 others(126): Show |
132 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.416-2135A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556841 | |||||||
chr21:17556899 | A | G | 328 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(325): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.416-2077A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556899 | |||||||
chr21:17556924 | T | C | 1 | a0001c0001t0003g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.416-2052T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17556924 | |||||||
chr21:17557001 | C | T | 3 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0011t0063g0159 |
3 | HG02055.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.416-1975C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557001 | |||||||
chr21:17557002 | G | T | 2 | a0001c0001t0001g0198 a0001c0001t0015g0265 |
2 | HG01257.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.416-1974G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557002 | |||||||
chr21:17557016 | G | A | 232 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.416-1960G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557016 | |||||||
chr21:17557227 | GGTTATAG others(3): Show |
G | 2 | a0001c0001t0002g0190 a0001c0001t0002g0222 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.416-1748_416-1739d others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557227 | |||||||
chr21:17557281 | G | C | 24 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0001t0003g0297 others(21): Show |
24 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-1695G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557281 | |||||||
chr21:17557355 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.416-1621C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557355 | |||||||
chr21:17557409 | T | G | 1 | a0001c0002t0004g0339 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.416-1567T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557409 | |||||||
chr21:17557426 | C | A | 234 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.416-1550C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557426 | |||||||
chr21:17557499 | C | T | 3 | a0001c0002t0021g0330 a0001c0002t0021g0331 a0001c0002t0034g0329 |
3 | HG02015.hp2 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.416-1477C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557499 | |||||||
chr21:17557522 | G | A | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1454G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557522 | |||||||
chr21:17557542 | T | A | 1 | a0001c0001t0019g0328 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.416-1434T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557542 | |||||||
chr21:17557637 | T | C | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.416-1339T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557637 | |||||||
chr21:17557671 | G | A | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-1305G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557671 | |||||||
chr21:17557752 | GAA | G | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1223_416-1222d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557752 | |||||||
chr21:17557851 | G | A | 1 | a0001c0002t0057g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.416-1125G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557851 | |||||||
chr21:17557911 | G | A | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-1065G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17557911 | |||||||
chr21:17558068 | A | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.416-908A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558068 | |||||||
chr21:17558081 | C | CT | 7 | a0001c0002t0013g0102 a0001c0002t0013g0103 a0001c0002t0013g0104 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-882dupT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | ||||||
chr21:17558081 | CT | C | 92 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(89): Show |
95 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.416-882delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | ||||||
chr21:17558081 | CTT | C | 203 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-883_416-882del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558081 | ||||||
chr21:17558093 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.416-883T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558093 | |||||||
chr21:17558094 | T | A | 203 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-882T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558094 | |||||||
chr21:17558115 | A | G | 203 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.416-861A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558115 | |||||||
chr21:17558118 | T | C | 1 | a0001c0002t0061g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.416-858T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558118 | |||||||
chr21:17558247 | G | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0302 a0001c0001t0017g0294 |
3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.416-729G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558247 | |||||||
chr21:17558247 | GC | G | 12 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(9): Show |
12 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-727delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 17558247 | ||||||
chr21:17558335 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.416-641A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558335 | |||||||
chr21:17558597 | A | T | 2 | a0001c0001t0003g0300 a0001c0001t0067g0015 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.416-379A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558597 | |||||||
chr21:17558614 | G | A | 12 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0005g0034 others(9): Show |
12 | HG00741.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-362G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558614 | |||||||
chr21:17558685 | ATT | A | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-290_416-289del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558685 | |||||||
chr21:17558747 | T | G | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-229T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558747 | |||||||
chr21:17558943 | T | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-33T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 3/6 | chr21 | 17558943 | |||||||
chr21:17559164 | C | T | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.571+33C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559164 | |||||||
chr21:17559176 | C | T | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.571+45C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559176 | |||||||
chr21:17559346 | AT | A | 46 | a0001c0001t0001g0211 a0001c0001t0001g0276 a0001c0001t0001g0278 others(43): Show |
47 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.571+225delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559346 | ||||||
chr21:17559356 | T | A | 19 | a0001c0001t0003g0067 a0001c0002t0008g0003 a0001c0002t0008g0042 others(16): Show |
20 | HG01884.hp2 HG01978.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.571+225T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559356 | |||||||
chr21:17559356 | TA | T | 197 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.571+231delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559356 | ||||||
chr21:17559358 | A | T | 3 | a0001c0001t0002g0193 a0001c0001t0002g0302 a0001c0001t0017g0294 |
3 | HG02451.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.571+227A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559358 | |||||||
chr21:17559387 | G | A | 1 | a0001c0004t0011g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571+256G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559387 | |||||||
chr21:17559419 | A | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.571+288A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559419 | |||||||
chr21:17559432 | T | C | 1 | a0001c0002t0062g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+301T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559432 | |||||||
chr21:17559611 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.571+480G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559611 | |||||||
chr21:17559641 | T | A | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.571+510T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559641 | |||||||
chr21:17559666 | TG | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0110 others(66): Show |
70 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.571+538delG | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559666 | ||||||
chr21:17559666 | TGG | T | 51 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
53 | HG00438.hp1 HG00733.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.571+537_571+538del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559666 | ||||||
chr21:17559667 | GGGT | G | 7 | a0001c0003t0009g0023 a0001c0003t0009g0025 a0001c0003t0009g0026 others(4): Show |
7 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+537_571+539del others(3): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559667 | |||||||
chr21:17559668 | G | GT | 6 | a0001c0002t0006g0100 a0001c0002t0006g0101 a0001c0002t0010g0180 others(3): Show |
6 | HG00642.hp1 HG01175.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+537_571+538ins others(1): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | |||||||
chr21:17559668 | G | T | 1 | a0001c0002t0006g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571+537G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | |||||||
chr21:17559668 | GGT | G | 173 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0053 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.571+538_571+539del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559668 | |||||||
chr21:17559669 | G | T | 50 | a0001c0001t0003g0022 a0001c0001t0003g0030 a0001c0001t0003g0049 others(47): Show |
52 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.571+538G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559669 | |||||||
chr21:17559674 | T | G | 7 | a0001c0001t0002g0093 a0001c0001t0002g0114 a0001c0001t0002g0173 others(4): Show |
7 | HG00621.hp2 HG01109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+543T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559674 | |||||||
chr21:17559675 | T | G | 75 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0017 others(72): Show |
77 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.571+544T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559675 | |||||||
chr21:17559677 | T | G | 5 | a0001c0001t0003g0030 a0001c0001t0003g0049 a0001c0001t0003g0057 others(2): Show |
5 | HG00544.hp2 HG00597.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.571+546T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559677 | |||||||
chr21:17559678 | T | G | 44 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(41): Show |
46 | HG00438.hp1 HG00733.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.571+547T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559678 | |||||||
chr21:17559691 | T | C | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.571+560T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559691 | |||||||
chr21:17559747 | C | T | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.571+616C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559747 | |||||||
chr21:17559865 | C | G | 319 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.571+734C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559865 | |||||||
chr21:17559869 | G | C | 1 | a0001c0002t0062g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+738G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559869 | |||||||
chr21:17559918 | C | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.572-784C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559918 | |||||||
chr21:17559968 | C | T | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.572-734C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17559968 | |||||||
chr21:17559971 | AT | A | 243 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.572-719delT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 17559971 | ||||||
chr21:17560012 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.572-690C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560012 | |||||||
chr21:17560034 | G | A | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.572-668G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560034 | |||||||
chr21:17560038 | G | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.572-664G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560038 | |||||||
chr21:17560117 | C | T | 1 | a0001c0001t0003g0306 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.572-585C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560117 | |||||||
chr21:17560125 | A | G | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.572-577A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560125 | |||||||
chr21:17560187 | G | A | 4 | a0001c0001t0002g0164 a0001c0001t0002g0167 a0001c0001t0002g0171 others(1): Show |
4 | NA18964.hp2 NA18971.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-515G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560187 | |||||||
chr21:17560222 | A | G | 1 | a0001c0001t0005g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.572-480A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560222 | |||||||
chr21:17560291 | A | C | 77 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0020 others(74): Show |
79 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.572-411A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560291 | |||||||
chr21:17560332 | G | T | 59 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(56): Show |
61 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.572-370G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560332 | |||||||
chr21:17560414 | G | A | 3 | a0001c0006t0032g0013 a0001c0006t0032g0014 a0001c0006t0078g0012 |
3 | HG01109.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.572-288G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560414 | |||||||
chr21:17560437 | G | C | 319 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.572-265G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560437 | |||||||
chr21:17560510 | A | T | 1 | a0001c0001t0068g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.572-192A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560510 | |||||||
chr21:17560616 | T | A | 235 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.572-86T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560616 | |||||||
chr21:17560654 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.572-48A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560654 | |||||||
chr21:17560658 | C | T | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.572-44C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560658 | |||||||
chr21:17560678 | G | C | 8 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.572-24G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 4/6 | chr21 | 17560678 | |||||||
chr21:17560918 | G | T | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+94G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17560918 | |||||||
chr21:17560989 | A | G | 1 | a0003c0010t0004g0340 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694+165A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17560989 | |||||||
chr21:17561018 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.694+194G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561018 | |||||||
chr21:17561062 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.694+238T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561062 | |||||||
chr21:17561217 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.695-121C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561217 | |||||||
chr21:17561243 | C | CAT | 327 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(324): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.695-95_695-94insAT | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561243 | |||||||
chr21:17561246 | G | C | 17 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(14): Show |
17 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.695-92G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561246 | |||||||
chr21:17561250 | A | G | 2 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.695-88A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561250 | |||||||
chr21:17561306 | A | G | 2 | a0001c0007t0002g0090 a0001c0007t0002g0091 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.695-32A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561306 | |||||||
chr21:17561307 | TA | T | 6 | a0001c0001t0003g0022 a0001c0001t0003g0085 a0001c0001t0003g0297 others(3): Show |
6 | HG01109.hp1 HG01361.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-30delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 5/6 | chr21 | 17561307 | |||||||
chr21:17561510 | A | G | 55 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(52): Show |
57 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.833+34A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561510 | |||||||
chr21:17561520 | T | A | 1 | a0001c0001t0001g0312 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.833+44T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561520 | |||||||
chr21:17561540 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.833+64C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561540 | |||||||
chr21:17561554 | C | A | 1 | a0001c0001t0048g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.833+78C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561554 | |||||||
chr21:17561586 | A | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+110A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561586 | |||||||
chr21:17561598 | C | T | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.833+122C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561598 | |||||||
chr21:17561668 | G | T | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.833+192G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561668 | |||||||
chr21:17561672 | C | T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.833+196C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561672 | |||||||
chr21:17561678 | C | G | 9 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(6): Show |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.833+202C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561678 | |||||||
chr21:17561761 | G | A | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+285G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561761 | |||||||
chr21:17561767 | G | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+291G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17561767 | |||||||
chr21:17562051 | G | T | 328 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(325): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.833+575G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562051 | |||||||
chr21:17562061 | T | C | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0304 |
3 | HG00408.hp2 NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.833+585T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562061 | |||||||
chr21:17562133 | A | C | 22 | a0001c0001t0002g0004 a0001c0001t0002g0107 a0001c0001t0002g0109 others(19): Show |
23 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.833+657A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562133 | |||||||
chr21:17562142 | A | T | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.833+666A>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562142 | |||||||
chr21:17562152 | T | TA | 319 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.833+682dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17562152 | ||||||
chr21:17562194 | CAGTG | C | 58 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(55): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.833+722_833+725del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17562194 | ||||||
chr21:17562221 | G | A | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.833+745G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562221 | |||||||
chr21:17562230 | G | T | 58 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(55): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.833+754G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562230 | |||||||
chr21:17562335 | TC | T | 82 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0017 others(79): Show |
84 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.833+860delC | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562335 | |||||||
chr21:17562351 | G | A | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.833+875G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562351 | |||||||
chr21:17562815 | A | G | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.833+1339A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562815 | |||||||
chr21:17562912 | T | C | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+1436T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562912 | |||||||
chr21:17562965 | C | T | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1489C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562965 | |||||||
chr21:17562981 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.833+1505C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17562981 | |||||||
chr21:17563079 | C | T | 82 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0017 others(79): Show |
84 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.833+1603C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563079 | |||||||
chr21:17563107 | T | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.833+1631T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563107 | |||||||
chr21:17563155 | GTTAA | G | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1683_833+1686d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563155 | ||||||
chr21:17563258 | C | G | 335 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(332): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.833+1782C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563258 | |||||||
chr21:17563260 | G | C | 319 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.833+1784G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563260 | |||||||
chr21:17563353 | G | C | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1877G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563353 | |||||||
chr21:17563360 | T | C | 1 | a0001c0002t0006g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.833+1884T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563360 | |||||||
chr21:17563440 | G | C | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.833+1964G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563440 | |||||||
chr21:17563484 | C | T | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-1944C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563484 | |||||||
chr21:17563576 | G | A | 14 | a0001c0002t0008g0003 a0001c0002t0008g0042 a0001c0002t0008g0061 others(11): Show |
15 | HG02015.hp2 HG02027.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.834-1852G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563576 | |||||||
chr21:17563663 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.834-1765C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563663 | |||||||
chr21:17563664 | G | A | 66 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(63): Show |
68 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.834-1764G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563664 | |||||||
chr21:17563668 | A | G | 119 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.834-1760A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563668 | |||||||
chr21:17563757 | C | T | 8 | a0001c0003t0009g0023 a0001c0003t0009g0024 a0001c0003t0009g0025 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1671C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563757 | |||||||
chr21:17563801 | T | C | 244 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.834-1627T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563801 | |||||||
chr21:17563813 | C | T | 1 | a0001c0001t0015g0251 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.834-1615C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563813 | |||||||
chr21:17563829 | C | T | 236 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.834-1599C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563829 | |||||||
chr21:17563834 | G | A | 1 | a0001c0002t0070g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.834-1594G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563834 | |||||||
chr21:17563897 | C | T | 1 | a0001c0004t0011g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.834-1531C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563897 | |||||||
chr21:17563940 | C | CA | 9 | a0001c0001t0002g0212 a0001c0001t0030g0019 a0001c0002t0057g0021 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.834-1467dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAA | 48 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0080 others(45): Show |
49 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.834-1468_834-1467d others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAA | 40 | a0001c0001t0002g0009 a0001c0001t0002g0092 a0001c0001t0002g0093 others(37): Show |
41 | HG00544.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.834-1469_834-1467d others(5): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAA | 32 | a0001c0001t0005g0036 a0001c0001t0005g0176 a0001c0001t0017g0294 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-1470_834-1467d others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA | 8 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1473_834-1467d others(9): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0023g0245 a0001c0001t0050g0216 a0001c0001t0055g0305 |
3 | NA18941.hp2 NA18975.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.834-1480_834-1467d others(16): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0023g0238 a0001c0001t0041g0256 a0001c0002t0062g0161 |
3 | HG03471.hp2 NA18940.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.834-1481_834-1467d others(17): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0263 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.834-1482_834-1467d others(18): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0242 others(3): Show |
6 | HG00140.hp2 HG01884.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.834-1483_834-1467d others(19): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(11): Show |
21 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0066 others(18): Show |
21 | HG00140.hp1 HG00408.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.834-1484_834-1467d others(20): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(12): Show |
34 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0124 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.834-1485_834-1467d others(21): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(13): Show |
27 | a0001c0001t0001g0007 a0001c0001t0001g0110 a0001c0001t0001g0112 others(24): Show |
28 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.834-1486_834-1467d others(22): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(14): Show |
8 | a0001c0001t0001g0223 a0001c0001t0001g0248 a0001c0001t0001g0260 others(5): Show |
8 | HG00621.hp1 HG01975.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1487_834-1467d others(23): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0280 a0001c0001t0001g0286 a0001c0001t0049g0277 others(1): Show |
4 | HG01975.hp1 NA19010.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.834-1467_834-1466i others(24): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0043g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(25): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0007g0233 a0001c0001t0007g0258 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.834-1467_834-1466i others(26): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0044g0207 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(27): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0007g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.834-1467_834-1466i others(29): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(22): Show |
1 | a0005c0012t0001g0279 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(31): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0268 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834-1467_834-1466i others(32): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563940 | CA | C | 54 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(51): Show |
56 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.834-1467delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17563940 | ||||||
chr21:17563963 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.834-1465G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17563963 | |||||||
chr21:17564066 | A | C | 2 | a0001c0001t0002g0017 a0001c0001t0030g0019 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.834-1362A>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564066 | |||||||
chr21:17564141 | T | A | 4 | a0001c0002t0006g0001 a0001c0002t0006g0115 a0001c0002t0006g0299 others(1): Show |
6 | HG01099.hp1 HG01192.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.834-1287T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564141 | |||||||
chr21:17564169 | T | TA | 7 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(4): Show |
8 | HG00544.hp1 HG02683.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.834-1258dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564169 | ||||||
chr21:17564194 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0292 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.834-1234C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564194 | |||||||
chr21:17564216 | G | A | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-1212G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564216 | |||||||
chr21:17564224 | G | A | 37 | a0001c0001t0028g0088 a0001c0001t0028g0089 a0001c0002t0006g0001 others(34): Show |
39 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.834-1204G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564224 | |||||||
chr21:17564251 | G | T | 1 | a0001c0001t0003g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.834-1177G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564251 | |||||||
chr21:17564321 | T | TA | 56 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.834-1094dupA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564321 | ||||||
chr21:17564321 | TA | T | 10 | a0001c0001t0002g0009 a0001c0001t0002g0153 a0001c0001t0002g0154 others(7): Show |
11 | HG00544.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.834-1094delA | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17564321 | ||||||
chr21:17564418 | T | G | 1 | a0001c0001t0005g0036 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.834-1010T>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564418 | |||||||
chr21:17564529 | T | C | 2 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.834-899T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564529 | |||||||
chr21:17564536 | A | G | 107 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(104): Show |
111 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.834-892A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564536 | |||||||
chr21:17564543 | G | T | 1 | a0001c0001t0003g0027 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.834-885G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564543 | |||||||
chr21:17564566 | C | T | 1 | a0001c0009t0075g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.834-862C>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564566 | |||||||
chr21:17564596 | G | C | 76 | a0001c0001t0001g0060 a0001c0001t0003g0002 a0001c0001t0003g0006 others(73): Show |
78 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.834-832G>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564596 | |||||||
chr21:17564633 | C | A | 2 | a0001c0001t0007g0233 a0001c0001t0007g0258 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.834-795C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564633 | |||||||
chr21:17564796 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.834-632G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564796 | |||||||
chr21:17564957 | A | G | 9 | a0001c0002t0006g0001 a0001c0002t0006g0099 a0001c0002t0006g0100 others(6): Show |
11 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.834-471A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564957 | |||||||
chr21:17564994 | C | G | 74 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(71): Show |
76 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.834-434C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17564994 | |||||||
chr21:17565003 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.834-425G>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565003 | |||||||
chr21:17565015 | G | T | 2 | a0001c0002t0059g0005 a0001c0002t0060g0005 |
2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-413G>T | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565015 | |||||||
chr21:17565057 | C | G | 1 | a0001c0001t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.834-371C>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565057 | |||||||
chr21:17565163 | C | A | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01069.hp2 HG01099.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-265C>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565163 | |||||||
chr21:17565239 | A | G | 7 | a0001c0002t0011g0105 a0001c0004t0011g0041 a0001c0004t0011g0079 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.834-189A>G | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565239 | |||||||
chr21:17565262 | T | A | 2 | a0001c0001t0002g0273 a0001c0001t0002g0292 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.834-166T>A | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565262 | |||||||
chr21:17565264 | T | C | 32 | a0001c0002t0004g0319 a0001c0002t0004g0321 a0001c0002t0004g0322 others(29): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.834-164T>C | CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | chr21 | 17565264 | |||||||
chr21:17565282 | GAC | G | 10 | a0001c0001t0003g0051 a0001c0002t0013g0102 a0001c0002t0013g0103 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.834-115_834-114del others(2): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACAC | G | 59 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0022 others(56): Show |
63 | HG00597.hp2 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.834-117_834-114del others(4): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACACAC | G | 10 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0052 others(7): Show |
10 | HG00438.hp1 HG00544.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-119_834-114del others(6): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACACACA others(1): Show |
G | 3 | a0001c0002t0027g0018 a0001c0002t0027g0142 a0001c0002t0062g0161 |
3 | HG01975.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.834-121_834-114del others(8): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACACACA others(3): Show |
G | 10 | a0001c0001t0002g0017 a0001c0001t0002g0020 a0001c0001t0030g0019 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.834-123_834-114del others(10): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACACACA others(5): Show |
G | 84 | a0001c0001t0001g0120 a0001c0001t0002g0004 a0001c0001t0002g0009 others(81): Show |
86 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.834-125_834-114del others(12): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 | ||||||
chr21:17565282 | GACACACA others(7): Show |
G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.834-127_834-114del others(14): Show |
CXADR | ENSG00000154639.19 | transcript | ENST00000284878.12 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 17565282 |