Item | Value |
---|---|
geneid | 84900 |
ensemblid | ENSG00000135119.15 |
hgncid | 25905 |
symbol | RNFT2 |
name | ring finger protein, transmembrane 2 |
refseq_nuc | NM_001382266.1 |
refseq_prot | NP_001369195.1 |
ensembl_nuc | ENST00000257575.9 |
ensembl_prot | ENSP00000257575.4 |
mane_status | MANE Select |
chr | chr12 |
start | 116738315 |
end | 116853631 |
strand | + |
ver | v1.2 |
region | chr12:116738315-116853631 |
region5000 | chr12:116733315-116858631 |
regionname0 | RNFT2_chr12_116738315_116853631 |
regionname5000 | RNFT2_chr12_116733315_116858631 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 444 | 264 | 92 | 42 | 89 | 2 | 37 | 60 | RNFT2_chr12_116733315_116858631 | RNFT2 | MWLFT others(439): Show |
chr12 | 116733315 | 116858631 |
a0002 | 0/0 | 444 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | MWLFT others(439): Show |
chr12 | 116733315 | 116858631 |
a0003 | 0/0 | 444 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | MWLFT others(439): Show |
chr12 | 116733315 | 116858631 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1332 | 146 | 27 | 26 | 63 | 1 | 28 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0002 | 0/0 | 1332 | 50 | 25 | 10 | 15 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0003 | 1/0 | 1332 | 17 | 8 | 2 | 3 | 1 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0004 | 0/0 | 1332 | 9 | 3 | 0 | 3 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0005 | 0/0 | 1332 | 7 | 7 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0006 | 0/0 | 1332 | 6 | 3 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0007 | 0/0 | 1332 | 6 | 5 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0008 | 0/0 | 1332 | 4 | 0 | 0 | 4 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0009 | 0/0 | 1332 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0011 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0012 | 0/0 | 1332 | 3 | 0 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0013 | 0/0 | 1332 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0014 | 0/0 | 1332 | 2 | 1 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0015 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0016 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0018 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0001c0019 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0002c0010 | 0/0 | 1332 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 | ||
a0003c0017 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | ATGTG others(1327): Show |
chr12 | 116733315 | 116858631 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5748 | 44 | 2 | 17 | 19 | 0 | 6 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0002 | 0/0 | 5737 | 18 | 8 | 2 | 8 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0003 | 0/0 | 5741 | 14 | 0 | 0 | 12 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0004 | 0/0 | 5727 | 12 | 2 | 0 | 4 | 0 | 6 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0005 | 0/0 | 5742 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0006 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0007 | 0/0 | 5727 | 7 | 0 | 0 | 5 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0008 | 0/0 | 5714 | 4 | 4 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5709): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0009 | 0/0 | 5741 | 5 | 0 | 2 | 0 | 0 | 3 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0010 | 0/0 | 5736 | 2 | 0 | 0 | 2 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0011 | 0/0 | 5737 | 3 | 3 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0012 | 0/0 | 5749 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0014 | 0/0 | 5738 | 3 | 2 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5733): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0015 | 0/0 | 5747 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5742): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0017 | 0/0 | 5748 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0019 | 0/0 | 5746 | 3 | 1 | 1 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5741): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0022 | 0/0 | 5749 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0024 | 0/0 | 5749 | 2 | 0 | 0 | 1 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0026 | 0/0 | 5728 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5723): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0027 | 0/0 | 5740 | 2 | 1 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0029 | 0/0 | 5742 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0038 | 0/1 | 5748 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0039 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0041 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5739): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0045 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5730): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0046 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5709): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0048 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0049 | 0/0 | 5727 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0057 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5739): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0058 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0059 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0061 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0062 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0070 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5733): Show |
chr12 | 116733315 | 116858631 |
a0001c0001t0072 | 0/0 | 5737 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0001 | 0/0 | 5748 | 13 | 1 | 3 | 9 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0002 | 0/0 | 5737 | 7 | 4 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0003 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0004 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0005 | 0/0 | 5742 | 5 | 4 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0008 | 0/0 | 5714 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5709): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0010 | 0/0 | 5736 | 2 | 1 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0011 | 0/0 | 5737 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0012 | 0/0 | 5749 | 2 | 0 | 2 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0015 | 0/0 | 5747 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5742): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0016 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5738): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0018 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5719): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0021 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0022 | 0/0 | 5749 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0033 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0042 | 0/0 | 5726 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5721): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0050 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0063 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0064 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0065 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0066 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0067 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5733): Show |
chr12 | 116733315 | 116858631 |
a0001c0002t0068 | 0/0 | 5739 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5734): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0002 | 0/0 | 5737 | 4 | 2 | 2 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0005 | 0/0 | 5742 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0006 | 1/0 | 5727 | 5 | 0 | 0 | 1 | 1 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0014 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5733): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0016 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5738): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0021 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0035 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0043 | 0/0 | 5728 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5723): Show |
chr12 | 116733315 | 116858631 |
a0001c0003t0044 | 0/0 | 5728 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5723): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0001 | 0/0 | 5748 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0012 | 0/0 | 5749 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5744): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0026 | 0/0 | 5728 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5723): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0029 | 0/0 | 5742 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0053 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5727): Show |
chr12 | 116733315 | 116858631 |
a0001c0004t0069 | 0/0 | 5738 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5733): Show |
chr12 | 116733315 | 116858631 |
a0001c0005t0013 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0005t0020 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0005t0030 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0005t0055 | 0/0 | 5740 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0005t0071 | 0/0 | 5730 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5725): Show |
chr12 | 116733315 | 116858631 |
a0001c0006t0005 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0006t0006 | 0/0 | 5727 | 2 | 0 | 0 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
a0001c0006t0031 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0006t0036 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0006t0051 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5720): Show |
chr12 | 116733315 | 116858631 |
a0001c0007t0005 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0007t0016 | 0/0 | 5743 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5738): Show |
chr12 | 116733315 | 116858631 |
a0001c0007t0025 | 0/0 | 5724 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5719): Show |
chr12 | 116733315 | 116858631 |
a0001c0007t0034 | 0/0 | 5742 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5737): Show |
chr12 | 116733315 | 116858631 |
a0001c0007t0047 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5718): Show |
chr12 | 116733315 | 116858631 |
a0001c0008t0003 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0008t0028 | 0/0 | 5741 | 2 | 0 | 0 | 2 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0008t0060 | 0/0 | 5740 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0009t0010 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0009t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5739): Show |
chr12 | 116733315 | 116858631 |
a0001c0009t0037 | 0/0 | 5743 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5738): Show |
chr12 | 116733315 | 116858631 |
a0001c0009t0052 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5720): Show |
chr12 | 116733315 | 116858631 |
a0001c0011t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5739): Show |
chr12 | 116733315 | 116858631 |
a0001c0011t0040 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5740): Show |
chr12 | 116733315 | 116858631 |
a0001c0011t0054 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5729): Show |
chr12 | 116733315 | 116858631 |
a0001c0012t0001 | 0/0 | 5748 | 3 | 0 | 1 | 0 | 0 | 2 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5743): Show |
chr12 | 116733315 | 116858631 |
a0001c0013t0013 | 0/0 | 5740 | 2 | 2 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5735): Show |
chr12 | 116733315 | 116858631 |
a0001c0013t0020 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5731): Show |
chr12 | 116733315 | 116858631 |
a0001c0014t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0014t0018 | 0/0 | 5724 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5719): Show |
chr12 | 116733315 | 116858631 |
a0001c0015t0002 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0016t0032 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0001c0018t0056 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5736): Show |
chr12 | 116733315 | 116858631 |
a0001c0019t0002 | 0/0 | 5737 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0002c0010t0002 | 0/0 | 5737 | 3 | 0 | 0 | 3 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5732): Show |
chr12 | 116733315 | 116858631 |
a0003c0017t0006 | 0/0 | 5727 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | GATTG others(5722): Show |
chr12 | 116733315 | 116858631 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0012g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0014g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0017g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0017g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0019g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0019g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0024g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0024g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0026g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0027g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0027g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0029g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0038g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0039g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0041g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0045g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0046g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0048g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0049g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0057g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0058g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0059g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0061g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0062g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0070g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0001t0072g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0015g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0022g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0033g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0042g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0050g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0063g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0064g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0065g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0066g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0067g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0002t0068g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0006g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0014g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0021g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0035g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0043g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0003t0044g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0012g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0026g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0029g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0053g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0004t0069g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0020g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0030g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0030g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0055g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0005t0071g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0031g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0036g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0006t0051g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0016g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0025g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0034g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0007t0047g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0008t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0008t0028g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0008t0028g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0008t0060g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0009t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0009t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0009t0037g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0009t0052g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0011t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0011t0040g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0011t0054g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0012t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0012t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0012t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0013t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0013t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0013t0020g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0014t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0014t0018g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0015t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0016t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0018t0056g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0001c0019t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0002c0010t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0002c0010t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0002c0010t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
a0003c0017t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0057 | g0220 | EUR | GBR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00140 | hp2 | a0001 | c0003 | t0006 | g0054 | EUR | GBR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0071 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00609 | hp1 | a0001 | c0001 | t0061 | g0090 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00621 | hp1 | a0001 | c0004 | t0001 | g0091 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00673 | hp1 | a0001 | c0001 | t0015 | g0112 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CHS | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00741 | hp1 | a0001 | c0006 | t0051 | g0013 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01074 | hp1 | a0001 | c0002 | t0012 | g0089 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01106 | hp1 | a0001 | c0014 | t0018 | g0019 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01109 | hp1 | a0001 | c0001 | t0070 | g0068 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01169 | hp1 | a0001 | c0001 | t0039 | g0219 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01169 | hp2 | a0001 | c0002 | t0063 | g0173 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01175 | hp1 | a0001 | c0012 | t0001 | g0123 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0261 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01243 | hp1 | a0001 | c0007 | t0016 | g0059 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01243 | hp2 | a0001 | c0002 | t0050 | g0004 | AMR | PUR | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0130 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01261 | hp2 | a0001 | c0001 | t0019 | g0187 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01358 | hp1 | a0001 | c0003 | t0002 | g0247 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01361 | hp1 | a0001 | c0002 | t0012 | g0014 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01884 | hp1 | a0001 | c0002 | t0065 | g0093 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01884 | hp2 | a0001 | c0007 | t0025 | g0009 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01891 | hp1 | a0001 | c0005 | t0030 | g0052 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01891 | hp2 | a0001 | c0013 | t0013 | g0046 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01975 | hp1 | a0001 | c0002 | t0067 | g0010 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02040 | hp1 | a0002 | c0010 | t0002 | g0254 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02055 | hp1 | a0001 | c0004 | t0069 | g0024 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02055 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02074 | hp1 | a0001 | c0001 | t0048 | g0241 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02132 | hp1 | a0001 | c0004 | t0001 | g0113 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02132 | hp2 | a0002 | c0010 | t0002 | g0002 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02135 | hp2 | a0002 | c0010 | t0002 | g0001 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02145 | hp1 | a0001 | c0007 | t0025 | g0057 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | CDX | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | CDX | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02257 | hp1 | a0001 | c0002 | t0018 | g0022 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0100 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02293 | hp1 | a0001 | c0002 | t0022 | g0252 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02451 | hp1 | a0001 | c0001 | t0027 | g0125 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02451 | hp2 | a0001 | c0006 | t0031 | g0067 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | KHV | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02572 | hp1 | a0001 | c0009 | t0037 | g0043 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02615 | hp2 | a0001 | c0006 | t0036 | g0018 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02630 | hp1 | a0001 | c0016 | t0032 | g0044 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02630 | hp2 | a0001 | c0009 | t0023 | g0028 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02647 | hp1 | a0001 | c0014 | t0002 | g0139 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0118 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02735 | hp1 | a0001 | c0001 | t0019 | g0153 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02735 | hp2 | a0001 | c0001 | t0027 | g0121 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02738 | hp1 | a0001 | c0003 | t0006 | g0165 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02738 | hp2 | a0001 | c0004 | t0029 | g0055 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02809 | hp1 | a0001 | c0011 | t0054 | g0011 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02809 | hp2 | a0001 | c0002 | t0011 | g0107 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02818 | hp1 | a0001 | c0002 | t0064 | g0263 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02818 | hp2 | a0001 | c0003 | t0035 | g0088 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02886 | hp2 | a0001 | c0002 | t0005 | g0062 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0099 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02896 | hp1 | a0001 | c0002 | t0068 | g0042 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02897 | hp2 | a0001 | c0002 | t0011 | g0097 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02922 | hp1 | a0001 | c0005 | t0055 | g0021 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02922 | hp2 | a0001 | c0002 | t0033 | g0150 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02965 | hp1 | a0001 | c0005 | t0071 | g0050 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02965 | hp2 | a0001 | c0003 | t0021 | g0040 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02970 | hp1 | a0001 | c0007 | t0005 | g0060 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02970 | hp2 | a0001 | c0005 | t0020 | g0161 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02976 | hp2 | a0001 | c0009 | t0052 | g0016 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03017 | hp2 | a0001 | c0012 | t0001 | g0239 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03130 | hp1 | a0001 | c0003 | t0005 | g0038 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03130 | hp2 | a0001 | c0001 | t0046 | g0114 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03139 | hp1 | a0001 | c0004 | t0002 | g0025 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03139 | hp2 | a0001 | c0007 | t0034 | g0061 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03195 | hp1 | a0001 | c0011 | t0023 | g0007 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03195 | hp2 | a0001 | c0003 | t0016 | g0035 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03209 | hp1 | a0001 | c0003 | t0014 | g0063 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03209 | hp2 | a0001 | c0001 | t0014 | g0039 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03225 | hp1 | a0001 | c0002 | t0066 | g0152 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03453 | hp1 | a0001 | c0004 | t0053 | g0015 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03453 | hp2 | a0001 | c0018 | t0056 | g0058 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0268 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0033 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03490 | hp1 | a0001 | c0003 | t0006 | g0204 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0156 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0169 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03491 | hp2 | a0001 | c0001 | t0045 | g0255 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0155 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03492 | hp2 | a0001 | c0001 | t0007 | g0170 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03516 | hp1 | a0001 | c0009 | t0010 | g0049 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03516 | hp2 | a0001 | c0015 | t0002 | g0020 | AFR | ESN | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0027 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03579 | hp1 | a0001 | c0005 | t0013 | g0186 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03654 | hp1 | a0001 | c0001 | t0058 | g0188 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03654 | hp2 | a0001 | c0006 | t0006 | g0218 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0167 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03688 | hp2 | a0001 | c0001 | t0024 | g0147 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0176 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0166 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03710 | hp1 | a0001 | c0001 | t0072 | g0120 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0183 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03831 | hp2 | a0001 | c0004 | t0012 | g0137 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03834 | hp2 | a0001 | c0006 | t0006 | g0066 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04184 | hp1 | a0001 | c0001 | t0026 | g0182 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04184 | hp2 | a0001 | c0001 | t0022 | g0225 | SAS | BEB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04228 | hp1 | a0001 | c0004 | t0026 | g0201 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | STU | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18522 | hp1 | a0001 | c0002 | t0005 | g0163 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18522 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0102 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18906 | hp2 | a0001 | c0013 | t0013 | g0159 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18945 | hp1 | a0001 | c0001 | t0017 | g0200 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18948 | hp1 | a0001 | c0008 | t0028 | g0214 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18950 | hp2 | a0001 | c0008 | t0028 | g0135 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18954 | hp2 | a0001 | c0001 | t0017 | g0175 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18956 | hp1 | a0001 | c0001 | t0041 | g0145 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18956 | hp2 | a0001 | c0003 | t0044 | g0221 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18960 | hp2 | a0001 | c0008 | t0060 | g0084 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18962 | hp1 | a0001 | c0001 | t0010 | g0226 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18971 | hp1 | a0001 | c0002 | t0010 | g0266 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18971 | hp2 | a0001 | c0004 | t0001 | g0083 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18975 | hp2 | a0001 | c0003 | t0006 | g0229 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18977 | hp1 | a0001 | c0001 | t0017 | g0213 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18977 | hp2 | a0001 | c0001 | t0049 | g0184 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18980 | hp1 | a0001 | c0001 | t0062 | g0148 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18980 | hp2 | a0001 | c0003 | t0043 | g0222 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18993 | hp1 | a0001 | c0001 | t0059 | g0108 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18993 | hp2 | a0001 | c0001 | t0024 | g0126 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18994 | hp1 | a0001 | c0002 | t0015 | g0081 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18999 | hp2 | a0001 | c0008 | t0003 | g0207 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19001 | hp2 | a0001 | c0019 | t0002 | g0267 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19012 | hp1 | a0001 | c0001 | t0029 | g0227 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19043 | hp1 | a0001 | c0013 | t0020 | g0098 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19043 | hp2 | a0001 | c0002 | t0021 | g0134 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19057 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0158 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19240 | hp1 | a0001 | c0002 | t0008 | g0140 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | YRI | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20129 | hp1 | a0001 | c0005 | t0030 | g0051 | AFR | ASW | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20129 | hp2 | a0001 | c0002 | t0005 | g0149 | AFR | ASW | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20905 | hp1 | a0001 | c0012 | t0001 | g0238 | SAS | GIH | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20905 | hp2 | a0003 | c0017 | t0006 | g0056 | SAS | GIH | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02109 | hp1 | a0001 | c0002 | t0016 | g0136 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02109 | hp2 | a0001 | c0002 | t0018 | g0047 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02486 | hp1 | a0001 | c0011 | t0040 | g0012 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02486 | hp2 | a0001 | c0006 | t0005 | g0017 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG02559 | hp2 | a0001 | c0002 | t0010 | g0132 | AFR | ACB | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03471 | hp1 | a0001 | c0007 | t0047 | g0053 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | MSL | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG06807 | hp1 | a0001 | c0005 | t0013 | g0006 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | USA | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA21309 | hp1 | a0001 | c0002 | t0042 | g0077 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
NA21309 | hp2 | a0001 | c0002 | t0005 | g0151 | AFR | LWK | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
homoSapiens | chm13v2 | a0001 | c0001 | t0038 | g0194 | REF | REF | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
homoSapiens | grch38p0 | a0001 | c0003 | t0006 | g0064 | REF | REF | RNFT2_chr12_116733315_116858631 | RNFT2 | chr12 | 116733315 | 116858631 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:116750145 | G | A | 1 | a0002 | 3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
missense_variant | MODERATE | c.388G>A | p.Val130Met | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 597/5727 | 388/1335 | 130/444 | chr12 | 116750145 | |||
chr12:116833847 | C | T | 1 | a0003 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.938C>T | p.Pro313Leu | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/11 | 1147/5727 | 938/1335 | 313/444 | chr12 | 116833847 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:116749865 | C | T | 1 | a0001c0019 | 1 | NA19001.hp2 | synonymous_variant | LOW | c.108C>T | p.Ser36Ser | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 317/5727 | 108/1335 | 36/444 | chr12 | 116749865 | |||
chr12:116750102 | T | C | 12 | a0001c0002 a0001c0004 a0001c0005 others(9): Show |
89 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(86): Show |
synonymous_variant | LOW | c.345T>C | p.His115His | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 554/5727 | 345/1335 | 115/444 | chr12 | 116750102 | |||
chr12:116750114 | C | T | 3 | a0001c0004 a0001c0007 a0001c0018 |
16 | HG00621.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
synonymous_variant | LOW | c.357C>T | p.Gly119Gly | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/11 | 566/5727 | 357/1335 | 119/444 | chr12 | 116750114 | |||
chr12:116766861 | G | A | 1 | a0001c0012 | 3 | HG01175.hp1 HG03017.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.675G>A | p.Ala225Ala | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/11 | 884/5727 | 675/1335 | 225/444 | chr12 | 116766861 | |||
chr12:116779336 | T | C | 13 | a0001c0001 a0001c0002 a0001c0004 others(10): Show |
234 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(231): Show |
synonymous_variant | LOW | c.870T>C | p.Ala290Ala | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/11 | 1079/5727 | 870/1335 | 290/444 | chr12 | 116779336 | |||
chr12:116833881 | C | T | 3 | a0001c0009 a0001c0011 a0001c0014 |
9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.972C>T | p.Asp324Asp | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/11 | 1181/5727 | 972/1335 | 324/444 | chr12 | 116833881 | |||
chr12:116849347 | C | T | 1 | a0001c0015 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1234C>T | p.Leu412Leu | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1443/5727 | 1234/1335 | 412/444 | chr12 | 116849347 | |||
chr12:116849385 | C | T | 4 | a0001c0005 a0001c0013 a0001c0016 others(1): Show |
12 | HG01891.hp1 HG01891.hp2 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.1272C>T | p.Val424Val | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1481/5727 | 1272/1335 | 424/444 | chr12 | 116849385 | |||
chr12:116849415 | C | T | 1 | a0001c0008 | 4 | NA18948.hp1 NA18950.hp2 NA18960.hp2 others(1): Show |
synonymous_variant | LOW | c.1302C>T | p.Asp434Asp | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1511/5727 | 1302/1335 | 434/444 | chr12 | 116849415 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:116740392 | C | T | 1 | a0001c0001t0072 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/11 | chr12 | 116740392 | |||||||
chr12:116740393 | G | A | 1 | a0001c0006t0031 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/11 | 105 | chr12 | 116740393 | ||||||
chr12:116849467 | C | T | 2 | a0001c0005t0030 a0001c0005t0071 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 19 | chr12 | 116849467 | ||||||
chr12:116849648 | C | T | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(34): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 200 | chr12 | 116849648 | ||||||
chr12:116849702 | G | A | 3 | a0001c0005t0020 a0001c0013t0020 a0001c0016t0032 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*254G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 254 | chr12 | 116849702 | ||||||
chr12:116849826 | C | T | 3 | a0001c0001t0019 a0001c0001t0057 a0001c0001t0058 |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*378C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 378 | chr12 | 116849826 | ||||||
chr12:116849845 | C | CTTCCTTC others(8): Show |
2 | a0001c0001t0027 a0001c0008t0060 |
3 | HG02451.hp1 HG02735.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTCC others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTCCTTC others(9): Show |
10 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0029 others(7): Show |
28 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTCC others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTCCTTT others(4): Show |
7 | a0001c0001t0010 a0001c0002t0010 a0001c0002t0033 others(4): Show |
9 | HG01169.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTCCTTT others(5): Show |
33 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(30): Show |
74 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTCCTTT others(6): Show |
15 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0017 others(12): Show |
77 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTCCTTT others(7): Show |
3 | a0001c0001t0024 a0001c0001t0041 a0001c0011t0040 |
4 | HG02486.hp1 HG03688.hp2 NA18956.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*400insCCTTTT others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 400 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0019 a0001c0001t0057 a0001c0001t0058 others(2): Show |
7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*413dupTTTTTT others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTTTTTT others(3): Show |
6 | a0001c0005t0013 a0001c0005t0020 a0001c0005t0030 others(3): Show |
9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*404_*413dupTTTTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849845 | C | CTTTTTTT others(4): Show |
2 | a0001c0016t0032 a0001c0018t0056 |
2 | HG02630.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*413dupTTTTTT others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | INFO_REALIGN_3_PRIME | chr12 | 116849845 | |||||
chr12:116849861 | T | A | 1 | a0001c0001t0059 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 413 | chr12 | 116849861 | ||||||
chr12:116849862 | A | T | 1 | a0001c0009t0052 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 414 | chr12 | 116849862 | ||||||
chr12:116849868 | A | G | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 420 | chr12 | 116849868 | ||||||
chr12:116850046 | T | C | 1 | a0001c0009t0052 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*598T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 598 | chr12 | 116850046 | ||||||
chr12:116850113 | G | A | 1 | a0001c0006t0036 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 665 | chr12 | 116850113 | ||||||
chr12:116850148 | C | CT | 5 | a0001c0001t0026 a0001c0003t0043 a0001c0003t0044 others(2): Show |
5 | HG00741.hp1 HG04184.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*724dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 725 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | |||||
chr12:116850148 | CTT | C | 6 | a0001c0001t0058 a0001c0002t0016 a0001c0003t0016 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*724delTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 723 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | |||||
chr12:116850148 | CTTT | C | 27 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0019 others(24): Show |
41 | HG01175.hp2 HG01261.hp2 HG01891.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*724delTTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 722 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | |||||
chr12:116850148 | CTTTT | C | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(48): Show |
170 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*724delTTTT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 721 | INFO_REALIGN_3_PRIME | chr12 | 116850148 | |||||
chr12:116850181 | G | T | 2 | a0001c0004t0053 a0001c0011t0054 |
2 | HG02809.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*733G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 733 | chr12 | 116850181 | ||||||
chr12:116850266 | C | T | 1 | a0001c0003t0035 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 818 | chr12 | 116850266 | ||||||
chr12:116850295 | C | T | 2 | a0001c0001t0009 a0001c0001t0027 |
7 | HG01109.hp2 HG01258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 847 | chr12 | 116850295 | ||||||
chr12:116850321 | AT | A | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*888delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 888 | INFO_REALIGN_3_PRIME | chr12 | 116850321 | |||||
chr12:116850502 | T | C | 2 | a0001c0002t0063 a0001c0004t0069 |
2 | HG01169.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1054T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1054 | chr12 | 116850502 | ||||||
chr12:116850565 | A | G | 1 | a0001c0009t0052 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1117 | chr12 | 116850565 | ||||||
chr12:116850613 | T | TTATTTTC | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1166_*1167insATTT others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | INFO_REALIGN_3_PRIME | chr12 | 116850613 | |||||
chr12:116850615 | C | A | 33 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(30): Show |
59 | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1167C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | chr12 | 116850615 | ||||||
chr12:116850615 | C | T | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1167C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1167 | chr12 | 116850615 | ||||||
chr12:116850620 | C | CTTTTTTC others(1): Show |
7 | a0001c0001t0012 a0001c0002t0012 a0001c0002t0068 others(4): Show |
8 | HG01074.hp1 HG01192.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | |||||
chr12:116850620 | C | CTTTTTTC others(7): Show |
1 | a0001c0001t0057 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | |||||
chr12:116850620 | C | CTTTTTTC others(8): Show |
1 | a0001c0001t0019 | 3 | HG01261.hp2 HG02055.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | |||||
chr12:116850620 | C | CTTTTTTC others(9): Show |
1 | a0001c0001t0058 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850620 | |||||
chr12:116850625 | T | TTCTTTTT others(1): Show |
3 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 |
6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850625 | |||||
chr12:116850625 | T | TTCTTTTT others(7): Show |
5 | a0001c0002t0018 a0001c0006t0051 a0001c0007t0025 others(2): Show |
7 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1178_*1179insCTTT others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1179 | INFO_REALIGN_3_PRIME | chr12 | 116850625 | |||||
chr12:116850629 | T | G | 1 | a0001c0001t0007 | 7 | HG00544.hp1 HG02523.hp2 HG03491.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1181T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1181 | chr12 | 116850629 | ||||||
chr12:116850632 | T | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0026 others(4): Show |
25 | HG00544.hp1 HG00673.hp2 HG02074.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1184T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1184 | chr12 | 116850632 | ||||||
chr12:116850635 | T | G | 19 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0026 others(16): Show |
40 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1187T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1187 | chr12 | 116850635 | ||||||
chr12:116850720 | C | T | 8 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(5): Show |
13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1272C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1272 | chr12 | 116850720 | ||||||
chr12:116850753 | G | A | 1 | a0001c0001t0061 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1305G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1305 | chr12 | 116850753 | ||||||
chr12:116850794 | AT | A | 12 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(9): Show |
17 | HG00741.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1356delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1356 | INFO_REALIGN_3_PRIME | chr12 | 116850794 | |||||
chr12:116850814 | G | A | 3 | a0001c0005t0020 a0001c0013t0020 a0001c0016t0032 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1366G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1366 | chr12 | 116850814 | ||||||
chr12:116850833 | ACGTTGGC others(9): Show |
A | 8 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(5): Show |
13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1402delGTTG others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1387 | INFO_REALIGN_3_PRIME | chr12 | 116850833 | |||||
chr12:116850890 | C | T | 1 | a0001c0001t0039 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1442 | chr12 | 116850890 | ||||||
chr12:116850937 | G | A | 1 | a0001c0008t0028 | 2 | NA18948.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1489G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1489 | chr12 | 116850937 | ||||||
chr12:116851024 | G | C | 9 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(6): Show |
14 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1576G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1576 | chr12 | 116851024 | ||||||
chr12:116851137 | C | T | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0026 others(5): Show |
26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1689C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1689 | chr12 | 116851137 | ||||||
chr12:116851138 | G | A | 1 | a0001c0003t0043 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1690G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1690 | chr12 | 116851138 | ||||||
chr12:116851173 | G | A | 2 | a0001c0001t0011 a0001c0002t0011 |
5 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1725G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1725 | chr12 | 116851173 | ||||||
chr12:116851229 | A | T | 1 | a0001c0001t0049 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1781A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1781 | chr12 | 116851229 | ||||||
chr12:116851230 | T | A | 100 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(97): Show |
253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*1782T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1782 | chr12 | 116851230 | ||||||
chr12:116851298 | T | C | 1 | a0001c0009t0052 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1850T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1850 | chr12 | 116851298 | ||||||
chr12:116851387 | G | A | 2 | a0001c0002t0064 a0001c0002t0065 |
2 | HG01884.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1939G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1939 | chr12 | 116851387 | ||||||
chr12:116851389 | A | T | 1 | a0001c0001t0017 | 3 | NA18945.hp1 NA18954.hp2 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1941A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1941 | chr12 | 116851389 | ||||||
chr12:116851435 | G | A | 3 | a0001c0005t0020 a0001c0013t0020 a0001c0016t0032 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1987G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 1987 | chr12 | 116851435 | ||||||
chr12:116851603 | G | T | 1 | a0001c0005t0055 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2155G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2155 | chr12 | 116851603 | ||||||
chr12:116851608 | C | T | 1 | a0001c0001t0046 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2160C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2160 | chr12 | 116851608 | ||||||
chr12:116851609 | G | A | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(34): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2161 | chr12 | 116851609 | ||||||
chr12:116851613 | G | A | 6 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(3): Show |
10 | HG00741.hp1 HG01106.hp1 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2165G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2165 | chr12 | 116851613 | ||||||
chr12:116851645 | C | T | 6 | a0001c0005t0013 a0001c0005t0030 a0001c0005t0055 others(3): Show |
9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2197C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2197 | chr12 | 116851645 | ||||||
chr12:116851794 | GGAAA | G | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(34): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2356_*2359delAAAG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2356 | INFO_REALIGN_3_PRIME | chr12 | 116851794 | |||||
chr12:116851808 | G | C | 16 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(13): Show |
80 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2360G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2360 | chr12 | 116851808 | ||||||
chr12:116851916 | C | G | 1 | a0001c0009t0037 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2468C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2468 | chr12 | 116851916 | ||||||
chr12:116852198 | G | A | 9 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(6): Show |
14 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2750G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2750 | chr12 | 116852198 | ||||||
chr12:116852291 | G | C | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2843G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2843 | chr12 | 116852291 | ||||||
chr12:116852350 | T | C | 102 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(99): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*2902T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2902 | chr12 | 116852350 | ||||||
chr12:116852377 | T | TTTCCCC | 16 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(13): Show |
80 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2932_*2937dupCCCC others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 2938 | INFO_REALIGN_3_PRIME | chr12 | 116852377 | |||||
chr12:116852551 | A | G | 3 | a0001c0005t0020 a0001c0013t0020 a0001c0016t0032 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3103A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3103 | chr12 | 116852551 | ||||||
chr12:116852628 | G | A | 11 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0046 others(8): Show |
18 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3180G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3180 | chr12 | 116852628 | ||||||
chr12:116852729 | G | T | 3 | a0001c0005t0020 a0001c0013t0020 a0001c0016t0032 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3281G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3281 | chr12 | 116852729 | ||||||
chr12:116852764 | C | T | 8 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(5): Show |
13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3316C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3316 | chr12 | 116852764 | ||||||
chr12:116852796 | T | C | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*3348T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3348 | chr12 | 116852796 | ||||||
chr12:116853120 | G | A | 1 | a0001c0001t0062 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3672G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3672 | chr12 | 116853120 | ||||||
chr12:116853330 | C | T | 1 | a0001c0001t0048 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3882C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3882 | chr12 | 116853330 | ||||||
chr12:116853334 | G | A | 39 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(36): Show |
93 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*3886G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3886 | chr12 | 116853334 | ||||||
chr12:116853334 | G | C | 3 | a0001c0001t0019 a0001c0001t0057 a0001c0001t0058 |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3886G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3886 | chr12 | 116853334 | ||||||
chr12:116853348 | A | T | 8 | a0001c0001t0008 a0001c0001t0046 a0001c0002t0008 others(5): Show |
13 | HG00741.hp1 HG01106.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3900A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3900 | chr12 | 116853348 | ||||||
chr12:116853438 | C | T | 1 | a0001c0009t0052 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3990C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 3990 | chr12 | 116853438 | ||||||
chr12:116853479 | G | A | 1 | a0001c0001t0048 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4031G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 4031 | chr12 | 116853479 | ||||||
chr12:116853540 | T | C | 1 | a0001c0002t0064 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4092T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 11/11 | 4092 | chr12 | 116853540 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:116738387 | A | AT | 180 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0119 others(177): Show |
180 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-154+26dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 116738387 | ||||||
chr12:116738509 | A | T | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-154+139A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738509 | |||||||
chr12:116738576 | A | G | 22 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0003g0085 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+206A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738576 | |||||||
chr12:116738619 | A | G | 1 | a0001c0002t0064g0263 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-154+249A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738619 | |||||||
chr12:116738708 | T | A | 2 | a0002c0010t0002g0001 a0002c0010t0002g0002 |
2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+338T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738708 | |||||||
chr12:116738747 | G | A | 43 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0003g0085 others(40): Show |
43 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.-154+377G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738747 | |||||||
chr12:116738784 | G | C | 2 | a0001c0005t0055g0021 a0001c0015t0002g0020 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-154+414G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738784 | |||||||
chr12:116738900 | G | A | 25 | a0001c0001t0001g0072 a0001c0001t0007g0070 a0001c0001t0007g0071 others(22): Show |
25 | HG00423.hp1 HG00544.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-154+530G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738900 | |||||||
chr12:116738918 | A | G | 3 | a0001c0006t0005g0017 a0001c0006t0036g0018 a0001c0014t0018g0019 |
3 | HG01106.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-154+548A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738918 | |||||||
chr12:116738942 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-154+572A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738942 | |||||||
chr12:116738986 | G | C | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-154+616G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116738986 | |||||||
chr12:116739021 | C | T | 8 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(5): Show |
8 | HG01192.hp1 HG01257.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+651C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739021 | |||||||
chr12:116739034 | T | C | 1 | a0001c0001t0061g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-154+664T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739034 | |||||||
chr12:116739122 | C | A | 2 | a0002c0010t0002g0001 a0002c0010t0002g0002 |
2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+752C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739122 | |||||||
chr12:116739206 | A | G | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-154+836A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739206 | |||||||
chr12:116739291 | G | A | 11 | a0001c0001t0002g0023 a0001c0002t0012g0014 a0001c0002t0012g0089 others(8): Show |
11 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-154+921G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739291 | |||||||
chr12:116739322 | A | C | 4 | a0001c0006t0036g0018 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG02040.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+952A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739322 | |||||||
chr12:116739413 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-153-932A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739413 | |||||||
chr12:116739530 | C | T | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-153-815C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739530 | |||||||
chr12:116739573 | C | T | 20 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0075 others(17): Show |
20 | HG00423.hp1 HG01099.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.-153-772C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739573 | |||||||
chr12:116739574 | G | A | 2 | a0001c0004t0002g0025 a0001c0004t0069g0024 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-771G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739574 | |||||||
chr12:116739606 | A | G | 1 | a0001c0001t0070g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-153-739A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739606 | |||||||
chr12:116739616 | G | C | 1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-153-729G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739616 | |||||||
chr12:116739887 | A | G | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-153-458A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116739887 | |||||||
chr12:116740059 | G | A | 242 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(239): Show |
242 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.-153-286G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740059 | |||||||
chr12:116740061 | G | T | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-284G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740061 | |||||||
chr12:116740168 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-153-177C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740168 | |||||||
chr12:116740284 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-153-61G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740284 | |||||||
chr12:116740307 | C | T | 4 | a0001c0001t0002g0023 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-38C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 1/10 | chr12 | 116740307 | |||||||
chr12:116740706 | T | C | 1 | a0001c0002t0065g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.24+185T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/10 | chr12 | 116740706 | |||||||
chr12:116740914 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.25-122C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 2/10 | chr12 | 116740914 | |||||||
chr12:116741530 | G | A | 2 | a0002c0010t0002g0001 a0002c0010t0002g0254 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.83+436G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741530 | |||||||
chr12:116741636 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0007g0071 |
2 | HG00544.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.83+542A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741636 | |||||||
chr12:116741840 | G | A | 226 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(223): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.83+746G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741840 | |||||||
chr12:116741951 | T | C | 2 | a0001c0001t0004g0095 a0001c0001t0004g0096 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.83+857T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116741951 | |||||||
chr12:116742030 | T | C | 5 | a0001c0001t0002g0023 a0001c0006t0005g0017 a0002c0010t0002g0001 others(2): Show |
5 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+936T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742030 | |||||||
chr12:116742265 | C | CT | 11 | a0001c0001t0001g0243 a0001c0001t0002g0048 a0001c0001t0003g0240 others(8): Show |
11 | HG00423.hp2 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+1191dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116742265 | ||||||
chr12:116742265 | CT | C | 5 | a0001c0001t0007g0070 a0001c0001t0045g0255 a0001c0002t0001g0250 others(2): Show |
5 | HG02897.hp2 HG03491.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+1191delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116742265 | ||||||
chr12:116742429 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.83+1335C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742429 | |||||||
chr12:116742505 | G | T | 2 | a0001c0012t0001g0238 a0001c0012t0001g0239 |
2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.83+1411G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742505 | |||||||
chr12:116742511 | T | C | 25 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0036 others(22): Show |
25 | HG01074.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+1417T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742511 | |||||||
chr12:116742548 | A | G | 5 | a0001c0001t0002g0023 a0001c0006t0005g0017 a0002c0010t0002g0001 others(2): Show |
5 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+1454A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742548 | |||||||
chr12:116742596 | G | A | 2 | a0001c0001t0004g0095 a0001c0001t0004g0096 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.83+1502G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742596 | |||||||
chr12:116742900 | T | C | 6 | a0001c0002t0018g0022 a0001c0002t0067g0010 a0001c0006t0051g0013 others(3): Show |
6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+1806T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116742900 | |||||||
chr12:116743039 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0002g0236 |
2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.83+1945C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743039 | |||||||
chr12:116743080 | C | CA | 7 | a0001c0002t0018g0022 a0001c0003t0002g0247 a0001c0003t0006g0054 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+2012dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | ||||||
chr12:116743080 | CAA | C | 17 | a0001c0001t0003g0106 a0001c0001t0004g0109 a0001c0001t0005g0246 others(14): Show |
17 | HG01175.hp2 HG01891.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+2011_83+2012del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | ||||||
chr12:116743080 | CAAA | C | 143 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0119 others(140): Show |
143 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(140): Show |
intron_variant | MODIFIER | c.83+2010_83+2012del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | ||||||
chr12:116743080 | CAAAA | C | 68 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(65): Show |
68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.83+2009_83+2012del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | ||||||
chr12:116743080 | CAAAAA | C | 6 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0262 others(3): Show |
6 | HG01257.hp1 HG01257.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2008_83+2012del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743080 | ||||||
chr12:116743136 | G | C | 1 | a0001c0004t0029g0055 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.83+2042G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743136 | |||||||
chr12:116743173 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.83+2079G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743173 | |||||||
chr12:116743197 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.83+2103G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743197 | |||||||
chr12:116743213 | T | TAAAAAAA others(3): Show |
8 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0002t0004g0268 others(5): Show |
8 | HG01884.hp1 HG02630.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+2141_83+2150dup others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(4): Show |
6 | a0001c0001t0024g0147 a0001c0001t0039g0219 a0001c0001t0057g0220 others(3): Show |
6 | HG00140.hp1 HG01169.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+2140_83+2150dup others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(5): Show |
20 | a0001c0001t0001g0069 a0001c0001t0001g0144 a0001c0001t0001g0215 others(17): Show |
20 | HG01192.hp1 HG01257.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+2139_83+2150dup others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(6): Show |
36 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0138 others(33): Show |
36 | HG00408.hp1 HG00438.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.83+2138_83+2150dup others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(7): Show |
15 | a0001c0001t0001g0198 a0001c0001t0001g0244 a0001c0001t0002g0023 others(12): Show |
15 | HG00408.hp2 HG00673.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+2137_83+2150dup others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(8): Show |
8 | a0001c0001t0001g0094 a0001c0001t0001g0256 a0001c0001t0004g0095 others(5): Show |
8 | HG00544.hp1 HG02055.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.83+2136_83+2150dup others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(9): Show |
9 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0195 others(6): Show |
9 | HG00544.hp2 HG00609.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2135_83+2150dup others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(10): Show |
9 | a0001c0001t0001g0193 a0001c0001t0002g0192 a0001c0001t0003g0117 others(6): Show |
9 | HG01109.hp2 HG01361.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2134_83+2150dup others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(11): Show |
6 | a0001c0001t0001g0190 a0001c0001t0003g0242 a0001c0001t0008g0041 others(3): Show |
6 | HG00423.hp2 HG01975.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+2133_83+2150dup others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(12): Show |
1 | a0001c0001t0002g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.83+2132_83+2150dup others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0015g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.83+2131_83+2150dup others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0003g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83+2130_83+2150dup others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0058g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.83+2128_83+2150dup others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743213 | T | TAAAAAAA others(17): Show |
1 | a0001c0001t0019g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.83+2127_83+2150dup others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743213 | ||||||
chr12:116743229 | AAAAAAAA others(9): Show |
A | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83+2136_83+2151del others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743229 | |||||||
chr12:116743231 | AAAAAAAA others(7): Show |
A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+2138_83+2151del others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743231 | |||||||
chr12:116743232 | AAAAAAAA others(6): Show |
A | 3 | a0001c0003t0006g0229 a0001c0003t0043g0222 a0001c0006t0005g0017 |
3 | HG02486.hp2 NA18975.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.83+2139_83+2151del others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743232 | |||||||
chr12:116743233 | AAAAAAAA others(5): Show |
A | 1 | a0001c0003t0044g0221 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.83+2140_83+2151del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743233 | |||||||
chr12:116743237 | AAAAAAAA others(1): Show |
A | 6 | a0001c0001t0001g0223 a0001c0001t0002g0179 a0001c0001t0015g0176 others(3): Show |
6 | HG00609.hp1 HG01169.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2144_83+2151del others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743237 | |||||||
chr12:116743238 | AAAAAAAC | A | 14 | a0001c0001t0001g0171 a0001c0001t0002g0178 a0001c0001t0004g0109 others(11): Show |
14 | HG00621.hp1 HG02074.hp1 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+2145_83+2151del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743238 | |||||||
chr12:116743239 | AAAAAAC | A | 29 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0002g0031 others(26): Show |
29 | HG01074.hp2 HG01106.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.83+2146_83+2151del others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743239 | |||||||
chr12:116743240 | AAAAAC | A | 16 | a0001c0001t0003g0160 a0001c0001t0004g0228 a0001c0001t0011g0099 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+2147_83+2151del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743240 | |||||||
chr12:116743241 | AAAAC | A | 6 | a0001c0001t0001g0092 a0001c0001t0009g0155 a0001c0001t0011g0157 others(3): Show |
6 | HG01109.hp1 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2148_83+2151del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743241 | |||||||
chr12:116743242 | AAAC | A | 21 | a0001c0001t0001g0230 a0001c0001t0003g0154 a0001c0002t0001g0075 others(18): Show |
21 | HG00621.hp2 HG01074.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+2149_83+2151del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743242 | |||||||
chr12:116743243 | AAC | A | 24 | a0001c0001t0001g0249 a0001c0001t0010g0226 a0001c0001t0014g0158 others(21): Show |
24 | HG00140.hp2 HG00423.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+2150_83+2151del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743243 | |||||||
chr12:116743244 | AC | A | 7 | a0001c0001t0001g0248 a0001c0001t0003g0162 a0001c0002t0001g0074 others(4): Show |
7 | HG01358.hp1 HG02145.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2152delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116743244 | ||||||
chr12:116743245 | C | A | 137 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(134): Show |
137 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.83+2151C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743245 | |||||||
chr12:116743406 | A | G | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.83+2312A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743406 | |||||||
chr12:116743414 | G | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83+2320G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743414 | |||||||
chr12:116743424 | G | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+2330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743424 | |||||||
chr12:116743452 | G | A | 1 | a0001c0008t0060g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.83+2358G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743452 | |||||||
chr12:116743721 | G | A | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83+2627G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743721 | |||||||
chr12:116743760 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.83+2666C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743760 | |||||||
chr12:116743874 | A | C | 7 | a0001c0002t0002g0110 a0001c0002t0002g0142 a0001c0002t0010g0132 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2780A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743874 | |||||||
chr12:116743885 | C | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+2791C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743885 | |||||||
chr12:116743903 | C | T | 232 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(229): Show |
232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.83+2809C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743903 | |||||||
chr12:116743986 | C | T | 3 | a0001c0001t0004g0185 a0001c0001t0048g0241 a0001c0001t0049g0184 |
3 | HG02074.hp1 NA18977.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.83+2892C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116743986 | |||||||
chr12:116744184 | C | A | 1 | a0001c0012t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.83+3090C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744184 | |||||||
chr12:116744225 | C | CA | 134 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(131): Show |
134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.83+3149dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116744225 | ||||||
chr12:116744225 | C | CAA | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0002g0236 others(4): Show |
7 | HG01261.hp1 HG01358.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+3148_83+3149dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116744225 | ||||||
chr12:116744239 | A | C | 2 | a0001c0002t0012g0014 a0001c0002t0012g0089 |
2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.83+3145A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744239 | |||||||
chr12:116744249 | G | A | 4 | a0001c0001t0002g0023 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG01192.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+3155G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744249 | |||||||
chr12:116744415 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.83+3321G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744415 | |||||||
chr12:116744737 | G | T | 6 | a0001c0002t0018g0022 a0001c0002t0067g0010 a0001c0006t0051g0013 others(3): Show |
6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+3643G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116744737 | |||||||
chr12:116745013 | T | C | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.83+3919T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745013 | |||||||
chr12:116745062 | T | C | 6 | a0001c0002t0018g0022 a0001c0002t0067g0010 a0001c0006t0051g0013 others(3): Show |
6 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+3968T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745062 | |||||||
chr12:116745087 | C | T | 2 | a0002c0010t0002g0001 a0002c0010t0002g0254 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.83+3993C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745087 | |||||||
chr12:116745118 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.83+4024G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745118 | |||||||
chr12:116745136 | G | C | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+4042G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745136 | |||||||
chr12:116745163 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.83+4069A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745163 | |||||||
chr12:116745173 | A | AT | 16 | a0001c0001t0001g0202 a0001c0001t0002g0023 a0001c0001t0008g0026 others(13): Show |
16 | HG01074.hp1 HG01192.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.83+4098dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | ||||||
chr12:116745173 | A | ATT | 214 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(211): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.83+4097_83+4098dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | ||||||
chr12:116745173 | A | ATTT | 9 | a0001c0001t0001g0193 a0001c0001t0001g0237 a0001c0001t0002g0234 others(6): Show |
9 | HG01106.hp1 HG01175.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+4096_83+4098dup others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116745173 | ||||||
chr12:116745277 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.83+4183C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745277 | |||||||
chr12:116745529 | G | A | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.84-4312G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745529 | |||||||
chr12:116745552 | T | C | 232 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(229): Show |
232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.84-4289T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745552 | |||||||
chr12:116745882 | T | C | 3 | a0001c0001t0014g0027 a0001c0001t0070g0068 a0001c0009t0023g0028 |
3 | HG01109.hp1 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84-3959T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745882 | |||||||
chr12:116745903 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.84-3938A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116745903 | |||||||
chr12:116746013 | G | A | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-3828G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746013 | |||||||
chr12:116746028 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.84-3813G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746028 | |||||||
chr12:116746186 | G | A | 141 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(138): Show |
141 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.84-3655G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746186 | |||||||
chr12:116746193 | C | T | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-3648C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746193 | |||||||
chr12:116746374 | A | G | 2 | a0001c0001t0004g0183 a0001c0001t0026g0182 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.84-3467A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746374 | |||||||
chr12:116746530 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0002g0236 a0001c0001t0024g0147 |
3 | HG01261.hp1 HG01358.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.84-3311G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746530 | |||||||
chr12:116746587 | C | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.84-3254C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746587 | |||||||
chr12:116746679 | A | G | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-3162A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746679 | |||||||
chr12:116746775 | G | A | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-3066G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746775 | |||||||
chr12:116746818 | G | A | 2 | a0001c0005t0055g0021 a0001c0015t0002g0020 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.84-3023G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746818 | |||||||
chr12:116746994 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0164 a0001c0002t0001g0111 |
3 | HG02004.hp2 HG02148.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.84-2847C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116746994 | |||||||
chr12:116747145 | C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-2696C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747145 | |||||||
chr12:116747482 | T | G | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-2359T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747482 | |||||||
chr12:116747624 | G | A | 5 | a0001c0002t0067g0010 a0001c0006t0051g0013 a0001c0007t0025g0009 others(2): Show |
5 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-2217G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747624 | |||||||
chr12:116747764 | C | T | 1 | a0001c0001t0057g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-2077C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747764 | |||||||
chr12:116747842 | G | A | 231 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(228): Show |
231 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.84-1999G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747842 | |||||||
chr12:116747918 | C | T | 1 | a0001c0009t0023g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.84-1923C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747918 | |||||||
chr12:116747983 | G | C | 5 | a0001c0002t0067g0010 a0001c0006t0051g0013 a0001c0007t0025g0009 others(2): Show |
5 | HG00741.hp1 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-1858G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116747983 | |||||||
chr12:116748008 | C | T | 230 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(227): Show |
230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.84-1833C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748008 | |||||||
chr12:116748104 | C | T | 1 | a0001c0003t0006g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.84-1737C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748104 | |||||||
chr12:116748171 | C | T | 1 | a0001c0001t0057g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-1670C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748171 | |||||||
chr12:116748207 | A | G | 223 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(220): Show |
223 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.84-1634A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748207 | |||||||
chr12:116748225 | G | A | 229 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(226): Show |
229 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.84-1616G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748225 | |||||||
chr12:116748311 | G | A | 2 | a0002c0010t0002g0001 a0002c0010t0002g0254 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.84-1530G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748311 | |||||||
chr12:116748428 | A | G | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-1413A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748428 | |||||||
chr12:116748444 | A | G | 1 | a0001c0002t0005g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84-1397A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748444 | |||||||
chr12:116748511 | A | G | 235 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(232): Show |
235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.84-1330A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748511 | |||||||
chr12:116748646 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.84-1195G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748646 | |||||||
chr12:116748895 | C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-946C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748895 | |||||||
chr12:116748923 | C | T | 1 | a0001c0001t0007g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.84-918C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748923 | |||||||
chr12:116748969 | G | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.84-872G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116748969 | |||||||
chr12:116749253 | T | C | 2 | a0001c0009t0010g0049 a0001c0013t0013g0046 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.84-588T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749253 | |||||||
chr12:116749259 | T | G | 8 | a0001c0001t0057g0220 a0001c0004t0053g0015 a0001c0005t0030g0051 others(5): Show |
8 | HG00140.hp1 HG01891.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-582T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749259 | |||||||
chr12:116749279 | TCC | T | 30 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0005g0062 others(27): Show |
30 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.84-555_84-554delCC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 116749279 | ||||||
chr12:116749287 | CA | C | 187 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(184): Show |
187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.84-553delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749287 | |||||||
chr12:116749288 | A | C | 39 | a0001c0001t0001g0235 a0001c0001t0002g0023 a0001c0001t0002g0236 others(36): Show |
39 | HG00423.hp1 HG01099.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.84-553A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749288 | |||||||
chr12:116749334 | G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.84-507G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749334 | |||||||
chr12:116749366 | C | T | 226 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(223): Show |
226 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.84-475C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749366 | |||||||
chr12:116749378 | A | G | 13 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(10): Show |
13 | HG00438.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-463A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 3/10 | chr12 | 116749378 | |||||||
chr12:116750390 | T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+83T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750390 | |||||||
chr12:116750634 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.550+327C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750634 | |||||||
chr12:116750660 | C | T | 204 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(201): Show |
204 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.550+353C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750660 | |||||||
chr12:116750754 | C | G | 226 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(223): Show |
226 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.550+447C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750754 | |||||||
chr12:116750768 | AAC | A | 9 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(6): Show |
9 | HG00140.hp1 HG00741.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+465_550+466del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750768 | ||||||
chr12:116750785 | ATATG | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+480_550+483del others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750785 | ||||||
chr12:116750797 | G | GTA | 4 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0057g0220 others(1): Show |
4 | HG00140.hp1 HG02055.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+501_550+502dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750797 | ||||||
chr12:116750797 | G | GTATATAT others(99): Show |
4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0011g0033 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+522_550+523ins others(106): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750797 | ||||||
chr12:116750799 | A | ATATATAT others(140): Show |
1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+500_550+501ins others(147): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750799 | ||||||
chr12:116750799 | A | ATATATAT others(119): Show |
3 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.550+522_550+523ins others(126): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750799 | ||||||
chr12:116750808 | TA | T | 9 | a0001c0001t0001g0144 a0001c0001t0002g0234 a0001c0001t0010g0233 others(6): Show |
9 | HG01106.hp1 HG01243.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+503delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750808 | ||||||
chr12:116750810 | A | T | 13 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0057g0220 others(10): Show |
13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+503A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750810 | |||||||
chr12:116750811 | TATATATA others(11): Show |
T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0048 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.550+513_550+530del others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750811 | ||||||
chr12:116750813 | T | C | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+506T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750813 | |||||||
chr12:116750813 | TATATATT others(21): Show |
T | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+507_550+534del others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750813 | |||||||
chr12:116750819 | T | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+512T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750819 | |||||||
chr12:116750819 | T | TTA | 6 | a0001c0003t0043g0222 a0001c0003t0044g0221 a0001c0007t0047g0053 others(3): Show |
6 | HG02040.hp1 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+521_550+522dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | ||||||
chr12:116750819 | T | TTATATAT others(59): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.550+522_550+523ins others(66): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | ||||||
chr12:116750819 | T | TTATATAT others(83): Show |
2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.550+522_550+523ins others(90): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | ||||||
chr12:116750819 | T | TTATATAT others(109): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550+522_550+523ins others(116): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750819 | ||||||
chr12:116750820 | T | A | 16 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0041g0145 others(13): Show |
16 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.550+513T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750820 | |||||||
chr12:116750822 | TATATATA | T | 8 | a0001c0001t0001g0259 a0001c0001t0004g0095 a0001c0001t0004g0096 others(5): Show |
8 | HG01978.hp1 HG02155.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.550+523_550+529del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750822 | ||||||
chr12:116750824 | TATATA | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0202 a0001c0001t0001g0211 others(10): Show |
13 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.550+523_550+527del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750824 | ||||||
chr12:116750824 | TATATAAT others(20): Show |
T | 18 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(15): Show |
18 | HG01192.hp2 HG02074.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.550+523_550+549del others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750824 | ||||||
chr12:116750826 | TATA | T | 125 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0092 others(122): Show |
125 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.550+523_550+525del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750826 | ||||||
chr12:116750826 | TATAATAT others(18): Show |
T | 10 | a0001c0001t0002g0236 a0001c0002t0004g0268 a0001c0002t0012g0014 others(7): Show |
10 | HG01074.hp1 HG01169.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.550+523_550+547del others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750826 | ||||||
chr12:116750828 | TA | T | 3 | a0001c0001t0024g0126 a0001c0002t0015g0081 a0001c0004t0012g0137 |
3 | HG03831.hp2 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.550+523delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750828 | ||||||
chr12:116750829 | A | AT | 4 | a0001c0003t0014g0063 a0001c0005t0030g0051 a0001c0005t0030g0052 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+522_550+523ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | |||||||
chr12:116750829 | A | G | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+522A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | |||||||
chr12:116750829 | A | T | 13 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0057g0220 others(10): Show |
13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+522A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750829 | |||||||
chr12:116750829 | AAT | A | 4 | a0001c0002t0018g0022 a0001c0005t0055g0021 a0001c0006t0051g0013 others(1): Show |
4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+531_550+532del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750829 | ||||||
chr12:116750830 | A | T | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+523A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750830 | |||||||
chr12:116750831 | T | A | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+524T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750831 | |||||||
chr12:116750831 | T | C | 9 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0002t0008g0140 others(6): Show |
9 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.550+524T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750831 | |||||||
chr12:116750831 | T | TA | 4 | a0001c0003t0014g0063 a0001c0005t0030g0051 a0001c0005t0030g0052 others(1): Show |
4 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+525dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750831 | ||||||
chr12:116750837 | TATTATAT others(3): Show |
T | 23 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(20): Show |
23 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.550+531_550+540del others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750837 | |||||||
chr12:116750839 | T | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550+532T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750839 | |||||||
chr12:116750839 | TTA | T | 4 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0057g0220 others(1): Show |
4 | HG00140.hp1 HG02055.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+543_550+544del others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750839 | ||||||
chr12:116750841 | A | T | 2 | a0001c0001t0001g0259 a0001c0001t0061g0090 |
2 | HG00609.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.550+534A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750841 | |||||||
chr12:116750841 | ATATATAT others(2): Show |
A | 146 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(143): Show |
146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.550+535_550+543del others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750841 | |||||||
chr12:116750842 | T | C | 7 | a0001c0001t0039g0219 a0001c0002t0018g0022 a0001c0005t0055g0021 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+535T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750842 | |||||||
chr12:116750847 | A | G | 11 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0002t0008g0140 others(8): Show |
11 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.550+540A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750847 | |||||||
chr12:116750848 | TATA | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0001t0002g0105 |
3 | HG02615.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.550+545_550+547del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750848 | ||||||
chr12:116750849 | AT | A | 23 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(20): Show |
23 | HG00423.hp1 HG01099.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.550+543delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750849 | |||||||
chr12:116750850 | T | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+543T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750850 | |||||||
chr12:116750851 | A | AAT | 7 | a0001c0002t0002g0034 a0001c0002t0004g0005 a0001c0002t0050g0004 others(4): Show |
7 | HG01243.hp2 HG02040.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+551_550+552dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750851 | ||||||
chr12:116750851 | A | AATATATA others(77): Show |
3 | a0001c0007t0025g0057 a0001c0007t0047g0053 a0001c0018t0056g0058 |
3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.550+562_550+563ins others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750851 | ||||||
chr12:116750851 | A | ATAAT | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+544_550+545ins others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | |||||||
chr12:116750851 | A | ATATATAT others(76): Show |
1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.550+544_550+545ins others(83): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | |||||||
chr12:116750851 | A | C | 171 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(168): Show |
171 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.550+544A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | |||||||
chr12:116750851 | A | T | 8 | a0001c0001t0039g0219 a0001c0002t0018g0022 a0001c0005t0030g0051 others(5): Show |
8 | HG00741.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.550+544A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750851 | |||||||
chr12:116750852 | ATATATAT others(22): Show |
A | 4 | a0001c0002t0018g0022 a0001c0005t0055g0021 a0001c0006t0051g0013 others(1): Show |
4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+553_550+581del others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750852 | ||||||
chr12:116750858 | A | G | 1 | a0001c0001t0039g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.550+551A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750858 | |||||||
chr12:116750859 | T | TATTATAT others(41): Show |
1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.550+552_550+553ins others(48): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750859 | |||||||
chr12:116750859 | TTATATAT others(25): Show |
T | 6 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0002t0008g0140 others(3): Show |
6 | HG01175.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+553_550+584del others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750859 | |||||||
chr12:116750860 | T | A | 1 | a0001c0001t0039g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.550+553T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750860 | |||||||
chr12:116750860 | T | G | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+553T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750860 | |||||||
chr12:116750861 | A | T | 3 | a0001c0001t0039g0219 a0001c0006t0005g0017 a0001c0006t0036g0018 |
3 | HG01169.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+554A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750861 | |||||||
chr12:116750862 | T | A | 3 | a0001c0001t0039g0219 a0001c0006t0005g0017 a0001c0006t0036g0018 |
3 | HG01169.hp1 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+555T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750862 | |||||||
chr12:116750862 | T | C | 40 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(37): Show |
40 | HG00140.hp1 HG01074.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+555T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750862 | |||||||
chr12:116750867 | A | G | 172 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(169): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.550+560A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750867 | |||||||
chr12:116750870 | TA | T | 3 | a0001c0001t0039g0219 a0001c0003t0002g0100 a0001c0003t0002g0101 |
3 | HG01074.hp2 HG01169.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.550+565delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750870 | ||||||
chr12:116750871 | A | T | 42 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(39): Show |
42 | HG00140.hp1 HG01074.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.550+564A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750871 | |||||||
chr12:116750874 | ATATATAT | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0007g0231 |
3 | HG00741.hp2 HG01106.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.550+575_550+581del others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750874 | ||||||
chr12:116750875 | TATATATT others(9): Show |
T | 3 | a0001c0001t0001g0235 a0001c0001t0003g0242 a0001c0002t0068g0042 |
3 | HG00423.hp2 HG01257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.550+575_550+590del others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750875 | ||||||
chr12:116750876 | ATATAT | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0206 others(4): Show |
7 | HG00438.hp1 HG02080.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+575_550+579del others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750876 | ||||||
chr12:116750877 | TATATTAT others(7): Show |
T | 91 | a0001c0001t0001g0092 a0001c0001t0001g0119 a0001c0001t0001g0138 others(88): Show |
91 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.550+575_550+588del others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750877 | ||||||
chr12:116750878 | A | G | 42 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(39): Show |
42 | HG00140.hp1 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.550+571A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750878 | |||||||
chr12:116750878 | ATAT | A | 3 | a0001c0001t0004g0096 a0001c0001t0004g0143 a0001c0012t0001g0123 |
3 | HG01175.hp1 HG02155.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.550+575_550+577del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750878 | ||||||
chr12:116750879 | TATTATAT others(5): Show |
T | 6 | a0001c0001t0002g0133 a0001c0001t0003g0127 a0001c0001t0003g0162 others(3): Show |
6 | HG00408.hp2 HG02155.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+575_550+586del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750879 | ||||||
chr12:116750881 | T | A | 2 | a0001c0006t0005g0017 a0001c0006t0036g0018 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.550+574T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750881 | |||||||
chr12:116750881 | T | TTA | 5 | a0001c0004t0001g0083 a0001c0006t0031g0067 a0001c0007t0025g0057 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.550+583_550+584dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATA | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(12): Show |
15 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.550+581_550+584dup others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(79): Show |
2 | a0001c0002t0001g0065 a0003c0017t0006g0056 |
2 | HG02258.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.550+594_550+595ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(101): Show |
1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(108): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(81): Show |
4 | a0001c0003t0006g0054 a0001c0004t0026g0201 a0001c0004t0029g0055 others(1): Show |
4 | HG00140.hp2 HG02738.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+584_550+585ins others(88): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(61): Show |
3 | a0001c0003t0006g0229 a0001c0003t0043g0222 a0001c0003t0044g0221 |
3 | NA18956.hp2 NA18975.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.550+584_550+585ins others(68): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(83): Show |
1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(90): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(143): Show |
2 | a0002c0010t0002g0001 a0002c0010t0002g0254 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.550+584_550+585ins others(150): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(116): Show |
1 | a0002c0010t0002g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(123): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(79): Show |
2 | a0001c0004t0002g0025 a0001c0004t0069g0024 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.550+584_550+585ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(79): Show |
1 | a0001c0007t0025g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.550+584_550+585ins others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(114): Show |
1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(121): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | T | TTATATAT others(112): Show |
1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.550+584_550+585ins others(119): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750881 | ||||||
chr12:116750881 | TTATATAT others(3): Show |
T | 59 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0122 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.550+575_550+584del others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750881 | |||||||
chr12:116750882 | T | A | 37 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(34): Show |
37 | HG01074.hp1 HG01074.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.550+575T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750882 | |||||||
chr12:116750887 | A | G | 4 | a0001c0002t0018g0022 a0001c0005t0055g0021 a0001c0006t0051g0013 others(1): Show |
4 | HG00741.hp1 HG02257.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+580A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750887 | |||||||
chr12:116750888 | TATA | T | 11 | a0001c0001t0002g0105 a0001c0001t0002g0236 a0001c0001t0007g0174 others(8): Show |
11 | HG01074.hp1 HG01243.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.550+585_550+587del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750888 | ||||||
chr12:116750890 | TA | T | 40 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0168 others(37): Show |
40 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.550+585delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750890 | ||||||
chr12:116750891 | A | AT | 7 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.550+584_550+585ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750891 | |||||||
chr12:116750899 | TA | T | 12 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(9): Show |
12 | HG00140.hp1 HG01099.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.550+593delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750899 | |||||||
chr12:116750900 | A | T | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+593A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750900 | |||||||
chr12:116750901 | TA | T | 15 | a0001c0002t0001g0073 a0001c0002t0001g0075 a0001c0002t0001g0078 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.550+595delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750901 | |||||||
chr12:116750902 | A | T | 23 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(20): Show |
23 | HG00140.hp1 HG01099.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.550+595A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750902 | |||||||
chr12:116750903 | TA | T | 3 | a0001c0002t0001g0074 a0001c0002t0063g0173 a0001c0003t0021g0040 |
3 | HG01169.hp2 HG02965.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.550+597delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750903 | |||||||
chr12:116750904 | A | AT | 4 | a0001c0001t0001g0256 a0001c0001t0002g0192 a0001c0001t0002g0209 others(1): Show |
4 | HG02273.hp2 NA18955.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+598dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750904 | ||||||
chr12:116750904 | A | T | 41 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(38): Show |
41 | HG00140.hp1 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.550+597A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750904 | |||||||
chr12:116750905 | TA | T | 28 | a0001c0001t0002g0036 a0001c0001t0002g0045 a0001c0001t0002g0048 others(25): Show |
28 | HG00438.hp1 HG01884.hp1 HG02148.hp2 others(25): Show |
intron_variant | MODIFIER | c.550+599delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750905 | |||||||
chr12:116750906 | A | AT | 22 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0197 others(19): Show |
22 | HG00544.hp2 HG00609.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.550+600dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750906 | ||||||
chr12:116750906 | A | T | 52 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(49): Show |
52 | HG00140.hp1 HG00423.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.550+599A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750906 | |||||||
chr12:116750907 | TA | T | 62 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0119 others(59): Show |
62 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.550+601delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750907 | |||||||
chr12:116750908 | A | AT | 27 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0198 others(24): Show |
27 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.550+610dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | ||||||
chr12:116750908 | A | T | 112 | a0001c0001t0001g0122 a0001c0001t0001g0141 a0001c0001t0001g0144 others(109): Show |
112 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.550+601A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750908 | |||||||
chr12:116750908 | AT | A | 10 | a0001c0001t0001g0069 a0001c0001t0002g0236 a0001c0001t0003g0106 others(7): Show |
10 | HG00621.hp2 HG01106.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.550+610delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | ||||||
chr12:116750908 | ATTT | A | 22 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(19): Show |
22 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.550+608_550+610del others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116750908 | ||||||
chr12:116750926 | G | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+619G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116750926 | |||||||
chr12:116751004 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.550+697C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751004 | |||||||
chr12:116751018 | T | G | 227 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(224): Show |
227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.550+711T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751018 | |||||||
chr12:116751075 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.550+768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751075 | |||||||
chr12:116751131 | G | T | 7 | a0001c0002t0004g0005 a0001c0002t0050g0004 a0001c0003t0014g0063 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+824G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751131 | |||||||
chr12:116751223 | T | C | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.550+916T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751223 | |||||||
chr12:116751408 | G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.550+1101G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751408 | |||||||
chr12:116751421 | G | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.550+1114G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751421 | |||||||
chr12:116751466 | C | T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0177 |
2 | HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.550+1159C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751466 | |||||||
chr12:116751593 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.550+1286C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751593 | |||||||
chr12:116751648 | G | A | 24 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(21): Show |
24 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.550+1341G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751648 | |||||||
chr12:116751681 | G | A | 227 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(224): Show |
227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.550+1374G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751681 | |||||||
chr12:116751836 | G | A | 67 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(64): Show |
67 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.550+1529G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751836 | |||||||
chr12:116751846 | A | G | 1 | a0001c0001t0041g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.550+1539A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751846 | |||||||
chr12:116751927 | T | C | 227 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(224): Show |
227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.550+1620T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116751927 | |||||||
chr12:116752045 | A | C | 17 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0002t0008g0140 others(14): Show |
17 | HG00741.hp1 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.550+1738A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752045 | |||||||
chr12:116752051 | T | C | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+1744T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752051 | |||||||
chr12:116752079 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.550+1772G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752079 | |||||||
chr12:116752137 | G | T | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.550+1830G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752137 | |||||||
chr12:116752196 | AAG | A | 227 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(224): Show |
227 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.551-1776_551-1775d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116752196 | ||||||
chr12:116752217 | G | A | 1 | a0001c0002t0002g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.551-1767G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752217 | |||||||
chr12:116752359 | T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.551-1625T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752359 | |||||||
chr12:116752445 | G | A | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-1539G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752445 | |||||||
chr12:116752455 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0217 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.551-1529T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752455 | |||||||
chr12:116752595 | C | A | 224 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(221): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.551-1389C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752595 | |||||||
chr12:116752652 | C | T | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-1332C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752652 | |||||||
chr12:116752808 | G | C | 6 | a0001c0001t0001g0168 a0001c0001t0004g0109 a0001c0001t0004g0166 others(3): Show |
6 | HG02683.hp2 HG03239.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-1176G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116752808 | |||||||
chr12:116753104 | T | A | 1 | a0001c0009t0023g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.551-880T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753104 | |||||||
chr12:116753110 | A | ATGGCGTT others(1): Show |
3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.551-872_551-865dup others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753110 | ||||||
chr12:116753124 | T | G | 10 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(7): Show |
10 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-860T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753124 | |||||||
chr12:116753142 | CTTTTTCT others(5): Show |
C | 2 | a0001c0002t0005g0062 a0001c0011t0040g0012 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.551-836_551-825del others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753142 | ||||||
chr12:116753148 | C | CT | 143 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(140): Show |
143 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.551-816dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | ||||||
chr12:116753148 | C | CTT | 29 | a0001c0001t0002g0236 a0001c0001t0004g0095 a0001c0001t0004g0096 others(26): Show |
29 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.551-817_551-816dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | ||||||
chr12:116753148 | CTTTTTTT others(4): Show |
C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.551-826_551-816del others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753148 | ||||||
chr12:116753152 | T | TTC | 25 | a0001c0001t0001g0092 a0001c0001t0001g0138 a0001c0001t0001g0164 others(22): Show |
25 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.551-831_551-830ins others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 116753152 | ||||||
chr12:116753153 | T | TC | 12 | a0001c0001t0001g0208 a0001c0001t0002g0133 a0001c0001t0002g0178 others(9): Show |
12 | HG00408.hp2 HG02155.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.551-831_551-830ins others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753153 | |||||||
chr12:116753182 | G | A | 2 | a0001c0001t0002g0236 a0001c0002t0012g0014 |
2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.551-802G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753182 | |||||||
chr12:116753220 | A | G | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-764A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753220 | |||||||
chr12:116753293 | G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.551-691G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753293 | |||||||
chr12:116753403 | G | A | 3 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0143 |
3 | HG02155.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.551-581G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753403 | |||||||
chr12:116753408 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.551-576C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753408 | |||||||
chr12:116753414 | G | A | 26 | a0001c0001t0001g0168 a0001c0001t0002g0023 a0001c0001t0004g0095 others(23): Show |
26 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.551-570G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753414 | |||||||
chr12:116753477 | T | C | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-507T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753477 | |||||||
chr12:116753654 | G | A | 246 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(243): Show |
246 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.551-330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753654 | |||||||
chr12:116753657 | G | A | 2 | a0001c0002t0063g0173 a0001c0002t0064g0263 |
2 | HG01169.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.551-327G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753657 | |||||||
chr12:116753862 | T | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-122T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753862 | |||||||
chr12:116753888 | G | A | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.551-96G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 4/10 | chr12 | 116753888 | |||||||
chr12:116754308 | T | G | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.627+248T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754308 | |||||||
chr12:116754322 | C | T | 218 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(215): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.627+262C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754322 | |||||||
chr12:116754339 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.627+279A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754339 | |||||||
chr12:116754572 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.627+512C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754572 | |||||||
chr12:116754916 | T | C | 2 | a0001c0002t0005g0062 a0001c0011t0040g0012 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.627+856T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116754916 | |||||||
chr12:116755245 | T | C | 218 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(215): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.627+1185T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755245 | |||||||
chr12:116755284 | T | C | 1 | a0001c0001t0019g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.627+1224T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755284 | |||||||
chr12:116755334 | A | G | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.627+1274A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755334 | |||||||
chr12:116755369 | T | TA | 3 | a0001c0001t0001g0205 a0001c0006t0005g0017 a0001c0006t0051g0013 |
3 | HG00741.hp1 HG02486.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.627+1309_627+1310i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755369 | |||||||
chr12:116755370 | T | A | 232 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(229): Show |
232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.627+1310T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755370 | |||||||
chr12:116755371 | T | A | 3 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0143 |
3 | HG02155.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.627+1311T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755371 | |||||||
chr12:116755408 | C | T | 218 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(215): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.627+1348C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755408 | |||||||
chr12:116755518 | C | G | 219 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(216): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.627+1458C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755518 | |||||||
chr12:116755946 | C | T | 3 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0009t0052g0016 |
3 | HG02976.hp2 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.627+1886C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116755946 | |||||||
chr12:116756054 | T | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+1994T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756054 | |||||||
chr12:116756284 | C | T | 8 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0003t0002g0100 others(5): Show |
8 | HG01074.hp2 HG01175.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2224C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756284 | |||||||
chr12:116756285 | G | A | 4 | a0001c0001t0009g0116 a0001c0001t0009g0130 a0001c0001t0009g0155 others(1): Show |
4 | HG01109.hp2 HG01258.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2225G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756285 | |||||||
chr12:116756306 | G | GT | 8 | a0001c0003t0006g0165 a0001c0005t0013g0006 a0001c0005t0030g0051 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+2255dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756306 | ||||||
chr12:116756306 | GT | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2255delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756306 | ||||||
chr12:116756309 | T | TTTTTTTG | 23 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(20): Show |
23 | HG00423.hp1 HG00423.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.627+2268_627+2274d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116756309 | ||||||
chr12:116756311 | T | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2251T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756311 | |||||||
chr12:116756366 | T | C | 3 | a0002c0010t0002g0001 a0002c0010t0002g0002 a0002c0010t0002g0254 |
3 | HG02040.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.627+2306T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756366 | |||||||
chr12:116756385 | G | A | 13 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(10): Show |
13 | HG00140.hp1 HG00741.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+2325G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756385 | |||||||
chr12:116756492 | A | T | 1 | a0001c0001t0004g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.627+2432A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756492 | |||||||
chr12:116756520 | G | A | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2460G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756520 | |||||||
chr12:116756539 | G | C | 11 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(8): Show |
11 | HG01106.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+2479G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756539 | |||||||
chr12:116756713 | T | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+2653T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756713 | |||||||
chr12:116756722 | C | T | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+2662C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756722 | |||||||
chr12:116756833 | C | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.627+2773C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756833 | |||||||
chr12:116756847 | T | C | 5 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+2787T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756847 | |||||||
chr12:116756870 | T | C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+2810T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756870 | |||||||
chr12:116756981 | A | T | 245 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(242): Show |
245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.627+2921A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116756981 | |||||||
chr12:116757091 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0230 a0001c0001t0010g0226 |
3 | HG03834.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.627+3031A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757091 | |||||||
chr12:116757392 | A | G | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+3332A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757392 | |||||||
chr12:116757402 | G | A | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+3342G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757402 | |||||||
chr12:116757413 | G | A | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+3353G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757413 | |||||||
chr12:116757579 | T | C | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+3519T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757579 | |||||||
chr12:116757583 | A | G | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+3523A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757583 | |||||||
chr12:116757838 | C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.627+3778C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757838 | |||||||
chr12:116757995 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+3935G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116757995 | |||||||
chr12:116758293 | A | C | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+4233A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758293 | |||||||
chr12:116758300 | C | T | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.627+4240C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758300 | |||||||
chr12:116758314 | A | G | 180 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(177): Show |
180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.627+4254A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758314 | |||||||
chr12:116758570 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0011g0033 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+4510C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758570 | |||||||
chr12:116758700 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.627+4640A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758700 | |||||||
chr12:116758701 | G | A | 8 | a0001c0002t0002g0129 a0001c0002t0005g0149 a0001c0002t0005g0151 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+4641G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758701 | |||||||
chr12:116758716 | G | C | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+4656G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758716 | |||||||
chr12:116758774 | G | T | 220 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(217): Show |
220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.627+4714G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758774 | |||||||
chr12:116758780 | C | T | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.627+4720C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758780 | |||||||
chr12:116758937 | T | A | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+4877T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116758937 | |||||||
chr12:116759096 | A | G | 14 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(11): Show |
14 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+5036A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759096 | |||||||
chr12:116759153 | G | C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.627+5093G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759153 | |||||||
chr12:116759284 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+5224C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759284 | |||||||
chr12:116759414 | T | A | 14 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(11): Show |
14 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+5354T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759414 | |||||||
chr12:116759499 | C | T | 27 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0002g0023 others(24): Show |
27 | HG01192.hp2 HG02074.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+5439C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759499 | |||||||
chr12:116759732 | C | T | 1 | a0001c0002t0002g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.627+5672C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759732 | |||||||
chr12:116759756 | A | G | 242 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(239): Show |
242 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.627+5696A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759756 | |||||||
chr12:116759797 | T | C | 2 | a0001c0006t0005g0017 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.627+5737T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759797 | |||||||
chr12:116759892 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.627+5832G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759892 | |||||||
chr12:116759921 | T | A | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.627+5861T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759921 | |||||||
chr12:116759941 | C | T | 1 | a0001c0001t0072g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.627+5881C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116759941 | |||||||
chr12:116760011 | C | T | 1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.627+5951C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760011 | |||||||
chr12:116760044 | A | G | 245 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(242): Show |
245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.627+5984A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760044 | |||||||
chr12:116760164 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0217 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.627+6104C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760164 | |||||||
chr12:116760332 | G | C | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.627+6272G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760332 | |||||||
chr12:116760421 | G | A | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+6361G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760421 | |||||||
chr12:116760449 | T | C | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628-6365T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760449 | |||||||
chr12:116760495 | G | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-6319G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760495 | |||||||
chr12:116760846 | C | T | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-5968C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760846 | |||||||
chr12:116760966 | A | G | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.628-5848A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760966 | |||||||
chr12:116760998 | C | T | 3 | a0001c0007t0025g0057 a0001c0007t0047g0053 a0001c0018t0056g0058 |
3 | HG02145.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.628-5816C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116760998 | |||||||
chr12:116761020 | G | A | 4 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0008g0140 others(1): Show |
4 | HG02976.hp2 HG03041.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-5794G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761020 | |||||||
chr12:116761106 | C | A | 10 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-5708C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761106 | |||||||
chr12:116761114 | G | A | 30 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0004g0095 others(27): Show |
30 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.628-5700G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761114 | |||||||
chr12:116761263 | C | T | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-5551C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761263 | |||||||
chr12:116761401 | G | T | 5 | a0001c0006t0005g0017 a0001c0006t0036g0018 a0001c0006t0051g0013 others(2): Show |
5 | HG00741.hp1 HG01106.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-5413G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761401 | |||||||
chr12:116761452 | T | C | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.628-5362T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761452 | |||||||
chr12:116761609 | G | T | 30 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0004g0095 others(27): Show |
30 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.628-5205G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761609 | |||||||
chr12:116761761 | C | T | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.628-5053C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761761 | |||||||
chr12:116761922 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-4892C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761922 | |||||||
chr12:116761930 | G | A | 6 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-4884G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116761930 | |||||||
chr12:116762064 | C | CA | 107 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(104): Show |
107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.628-4734dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | ||||||
chr12:116762064 | CA | C | 23 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0036 others(20): Show |
23 | HG00140.hp1 HG01074.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-4734delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | ||||||
chr12:116762064 | CAA | C | 29 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0004g0095 others(26): Show |
29 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(26): Show |
intron_variant | MODIFIER | c.628-4735_628-4734d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762064 | ||||||
chr12:116762107 | T | G | 35 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0004g0095 others(32): Show |
35 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.628-4707T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762107 | |||||||
chr12:116762403 | C | CA | 183 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(180): Show |
183 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.628-4399dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762403 | ||||||
chr12:116762403 | C | CAA | 8 | a0001c0001t0001g0069 a0001c0001t0001g0119 a0001c0001t0001g0223 others(5): Show |
8 | HG00609.hp1 HG00609.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-4400_628-4399d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762403 | ||||||
chr12:116762416 | C | G | 4 | a0001c0005t0013g0006 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-4398C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762416 | |||||||
chr12:116762580 | A | AT | 19 | a0001c0001t0001g0092 a0001c0001t0001g0197 a0001c0001t0001g0232 others(16): Show |
19 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.628-4217dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | ||||||
chr12:116762580 | A | ATT | 25 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(22): Show |
25 | HG01243.hp1 HG02074.hp1 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.628-4218_628-4217d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | ||||||
chr12:116762580 | A | ATTT | 8 | a0001c0001t0001g0168 a0001c0001t0004g0167 a0001c0001t0004g0172 others(5): Show |
8 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-4219_628-4217d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | ||||||
chr12:116762580 | AT | A | 8 | a0001c0001t0001g0190 a0001c0001t0001g0224 a0001c0001t0008g0026 others(5): Show |
8 | HG01074.hp2 HG01975.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-4217delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116762580 | ||||||
chr12:116762639 | G | C | 2 | a0001c0002t0001g0251 a0001c0002t0002g0181 |
2 | NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.628-4175G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762639 | |||||||
chr12:116762802 | G | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-4012G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762802 | |||||||
chr12:116762854 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-3960C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762854 | |||||||
chr12:116762934 | T | G | 5 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(2): Show |
5 | HG01192.hp1 HG01257.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-3880T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762934 | |||||||
chr12:116762978 | A | C | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.628-3836A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116762978 | |||||||
chr12:116763003 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0237 |
2 | HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.628-3811T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763003 | |||||||
chr12:116763046 | C | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0002t0004g0268 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-3768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763046 | |||||||
chr12:116763176 | GA | G | 219 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(216): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.628-3624delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763176 | ||||||
chr12:116763195 | A | C | 3 | a0001c0001t0002g0236 a0001c0002t0012g0014 a0001c0002t0012g0089 |
3 | HG01074.hp1 HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.628-3619A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763195 | |||||||
chr12:116763605 | AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0215 |
3 | HG01361.hp2 HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.628-3197_628-3184d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763605 | ||||||
chr12:116763619 | C | CA | 200 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(197): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.628-3185dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763619 | ||||||
chr12:116763651 | C | T | 1 | a0001c0013t0013g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.628-3163C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763651 | |||||||
chr12:116763652 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.628-3162G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763652 | |||||||
chr12:116763766 | G | A | 8 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(5): Show |
8 | HG01243.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-3048G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763766 | |||||||
chr12:116763783 | A | G | 16 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(13): Show |
16 | HG01891.hp1 HG02040.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.628-3031A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763783 | |||||||
chr12:116763784 | A | C | 3 | a0001c0002t0063g0173 a0001c0002t0064g0263 a0001c0002t0065g0093 |
3 | HG01169.hp2 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.628-3030A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763784 | |||||||
chr12:116763785 | A | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.628-3029A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763785 | |||||||
chr12:116763794 | C | A | 18 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(15): Show |
18 | HG02074.hp1 HG02523.hp2 HG02683.hp2 others(15): Show |
intron_variant | MODIFIER | c.628-3020C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763794 | |||||||
chr12:116763794 | C | CG | 18 | a0001c0001t0001g0206 a0001c0001t0001g0217 a0001c0001t0001g0258 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-3012dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763794 | ||||||
chr12:116763794 | C | G | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.628-3020C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763794 | |||||||
chr12:116763794 | CG | C | 45 | a0001c0001t0001g0072 a0001c0001t0001g0141 a0001c0001t0001g0190 others(42): Show |
45 | HG01074.hp2 HG01169.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.628-3012delG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763794 | ||||||
chr12:116763795 | G | C | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.628-3019G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763795 | |||||||
chr12:116763802 | GA | G | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(12): Show |
15 | HG01891.hp1 HG02040.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.628-3009delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116763802 | ||||||
chr12:116763899 | A | C | 21 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(18): Show |
21 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.628-2915A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763899 | |||||||
chr12:116763950 | C | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.628-2864C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763950 | |||||||
chr12:116763970 | T | C | 48 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(45): Show |
48 | HG00140.hp1 HG01074.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.628-2844T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116763970 | |||||||
chr12:116764059 | A | G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.628-2755A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764059 | |||||||
chr12:116764062 | G | T | 1 | a0001c0001t0057g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.628-2752G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764062 | |||||||
chr12:116764279 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-2535G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764279 | |||||||
chr12:116764340 | C | T | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-2474C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764340 | |||||||
chr12:116764352 | A | AT | 14 | a0001c0002t0018g0022 a0001c0003t0002g0100 a0001c0003t0002g0101 others(11): Show |
14 | HG01074.hp2 HG01891.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-2452dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116764352 | ||||||
chr12:116764518 | G | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.628-2296G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764518 | |||||||
chr12:116764644 | C | T | 18 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-2170C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764644 | |||||||
chr12:116764686 | G | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2128G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764686 | |||||||
chr12:116764753 | A | G | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2061A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764753 | |||||||
chr12:116764758 | G | C | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.628-2056G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764758 | |||||||
chr12:116764764 | C | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0002t0004g0268 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2050C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764764 | |||||||
chr12:116764781 | A | G | 69 | a0001c0001t0001g0171 a0001c0001t0002g0031 a0001c0001t0002g0032 others(66): Show |
69 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(66): Show |
intron_variant | MODIFIER | c.628-2033A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764781 | |||||||
chr12:116764823 | C | T | 105 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(102): Show |
105 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(102): Show |
intron_variant | MODIFIER | c.628-1991C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764823 | |||||||
chr12:116764888 | G | A | 2 | a0001c0012t0001g0123 a0001c0012t0001g0239 |
2 | HG01175.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.628-1926G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116764888 | |||||||
chr12:116765016 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.628-1798C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765016 | |||||||
chr12:116765017 | G | A | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628-1797G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765017 | |||||||
chr12:116765418 | C | T | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.628-1396C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765418 | |||||||
chr12:116765840 | G | A | 2 | a0001c0001t0003g0117 a0001c0001t0003g0240 |
2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.628-974G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116765840 | |||||||
chr12:116766010 | G | A | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-804G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766010 | |||||||
chr12:116766091 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.628-723G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766091 | |||||||
chr12:116766116 | T | TA | 48 | a0001c0001t0001g0171 a0001c0001t0002g0031 a0001c0001t0002g0032 others(45): Show |
48 | HG00140.hp1 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-693dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 116766116 | ||||||
chr12:116766121 | A | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0014t0018g0019 |
3 | HG01106.hp1 HG02004.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.628-693A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766121 | |||||||
chr12:116766122 | T | A | 40 | a0001c0001t0001g0171 a0001c0001t0001g0216 a0001c0001t0001g0259 others(37): Show |
40 | HG01243.hp2 HG01884.hp2 HG01978.hp1 others(37): Show |
intron_variant | MODIFIER | c.628-692T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766122 | |||||||
chr12:116766123 | T | A | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-691T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766123 | |||||||
chr12:116766125 | T | G | 7 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(4): Show |
7 | HG01243.hp1 HG02965.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-689T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766125 | |||||||
chr12:116766275 | T | A | 8 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-539T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766275 | |||||||
chr12:116766477 | A | G | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.628-337A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766477 | |||||||
chr12:116766600 | T | C | 2 | a0001c0006t0005g0017 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.628-214T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766600 | |||||||
chr12:116766753 | C | T | 1 | a0001c0001t0062g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.628-61C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 5/10 | chr12 | 116766753 | |||||||
chr12:116767053 | T | TTA | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+147_728+148dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116767053 | ||||||
chr12:116767130 | T | G | 2 | a0001c0005t0030g0051 a0001c0005t0030g0052 |
2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.728+216T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767130 | |||||||
chr12:116767169 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.728+255T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767169 | |||||||
chr12:116767339 | T | C | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+425T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767339 | |||||||
chr12:116767380 | G | A | 24 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(21): Show |
24 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.728+466G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767380 | |||||||
chr12:116767476 | C | T | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+562C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767476 | |||||||
chr12:116767552 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+638G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767552 | |||||||
chr12:116767565 | T | TG | 8 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.728+652dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116767565 | ||||||
chr12:116767567 | T | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+653T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767567 | |||||||
chr12:116767568 | T | G | 242 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(239): Show |
242 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.728+654T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767568 | |||||||
chr12:116767569 | T | G | 40 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(37): Show |
40 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.728+655T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767569 | |||||||
chr12:116767665 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.728+751C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767665 | |||||||
chr12:116767813 | C | T | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+899C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767813 | |||||||
chr12:116767814 | G | A | 1 | a0001c0006t0005g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.728+900G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767814 | |||||||
chr12:116767894 | C | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+980C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767894 | |||||||
chr12:116767930 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+1016G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767930 | |||||||
chr12:116767986 | T | A | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.728+1072T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116767986 | |||||||
chr12:116768099 | C | CT | 64 | a0001c0001t0001g0171 a0001c0001t0001g0208 a0001c0001t0002g0031 others(61): Show |
64 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.728+1201dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768099 | ||||||
chr12:116768099 | C | CTT | 6 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0007g0169 others(3): Show |
6 | HG02055.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.728+1200_728+1201d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768099 | ||||||
chr12:116768145 | G | A | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+1231G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768145 | |||||||
chr12:116768223 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.728+1309C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768223 | |||||||
chr12:116768247 | C | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+1333C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768247 | |||||||
chr12:116768305 | T | A | 1 | a0001c0001t0004g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.728+1391T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768305 | |||||||
chr12:116768321 | G | A | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1407G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768321 | |||||||
chr12:116768454 | C | T | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+1540C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768454 | |||||||
chr12:116768713 | A | AT | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1809dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768713 | ||||||
chr12:116768728 | T | TTCTC | 16 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(13): Show |
16 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.728+1820_728+1823d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768728 | ||||||
chr12:116768736 | C | CTCTT | 30 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(27): Show |
30 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.728+1823_728+1824i others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116768736 | ||||||
chr12:116768738 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.728+1824T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768738 | |||||||
chr12:116768753 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.728+1839C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768753 | |||||||
chr12:116768770 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.728+1856G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768770 | |||||||
chr12:116768857 | A | C | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(9): Show |
12 | HG01175.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+1943A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768857 | |||||||
chr12:116768951 | A | G | 48 | a0001c0001t0001g0171 a0001c0001t0002g0031 a0001c0001t0002g0032 others(45): Show |
48 | HG00140.hp1 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.728+2037A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768951 | |||||||
chr12:116768982 | C | T | 149 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(146): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.728+2068C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116768982 | |||||||
chr12:116769082 | G | A | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+2168G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769082 | |||||||
chr12:116769149 | G | A | 31 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(28): Show |
31 | HG01243.hp2 HG02074.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.728+2235G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769149 | |||||||
chr12:116769197 | A | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0205 a0001c0001t0001g0211 others(2): Show |
5 | HG00408.hp1 HG02080.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+2283A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769197 | |||||||
chr12:116769225 | A | G | 74 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(71): Show |
74 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.728+2311A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769225 | |||||||
chr12:116769283 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.728+2369G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769283 | |||||||
chr12:116769345 | G | A | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.728+2431G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769345 | |||||||
chr12:116769349 | T | C | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+2435T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769349 | |||||||
chr12:116769403 | A | G | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+2489A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769403 | |||||||
chr12:116769611 | C | T | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+2697C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769611 | |||||||
chr12:116769754 | G | A | 34 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(31): Show |
34 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.728+2840G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769754 | |||||||
chr12:116769774 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.728+2860G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769774 | |||||||
chr12:116769782 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.728+2868A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769782 | |||||||
chr12:116769943 | G | T | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0143 others(2): Show |
5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+3029G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116769943 | |||||||
chr12:116770101 | A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728+3187A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770101 | |||||||
chr12:116770263 | C | T | 2 | a0001c0007t0025g0057 a0001c0007t0047g0053 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.728+3349C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770263 | |||||||
chr12:116770294 | A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.728+3380A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770294 | |||||||
chr12:116770394 | A | C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+3480A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770394 | |||||||
chr12:116770547 | T | C | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3633T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770547 | |||||||
chr12:116770633 | C | T | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0008g0026 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+3719C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770633 | |||||||
chr12:116770644 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3730A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770644 | |||||||
chr12:116770703 | G | A | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.728+3789G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770703 | |||||||
chr12:116770759 | A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.728+3845A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770759 | |||||||
chr12:116770937 | G | A | 2 | a0001c0005t0020g0161 a0001c0013t0020g0098 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.728+4023G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116770937 | |||||||
chr12:116771033 | G | A | 9 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(6): Show |
9 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.728+4119G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771033 | |||||||
chr12:116771071 | A | G | 1 | a0001c0003t0016g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.728+4157A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771071 | |||||||
chr12:116771180 | T | G | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+4266T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771180 | |||||||
chr12:116771199 | G | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.728+4285G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771199 | |||||||
chr12:116771340 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.728+4426G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771340 | |||||||
chr12:116771430 | G | A | 32 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(29): Show |
32 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.728+4516G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771430 | |||||||
chr12:116771457 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.728+4543C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771457 | |||||||
chr12:116771460 | TA | T | 92 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0122 others(89): Show |
92 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.728+4581delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAA | T | 10 | a0001c0001t0011g0157 a0001c0002t0011g0107 a0001c0003t0005g0038 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.728+4579_728+4581d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAA | T | 14 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(11): Show |
14 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.728+4578_728+4581d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(1): Show |
T | 25 | a0001c0001t0001g0171 a0001c0001t0003g0106 a0001c0001t0004g0109 others(22): Show |
25 | HG02071.hp2 HG02074.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.728+4574_728+4581d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(2): Show |
T | 8 | a0001c0001t0001g0262 a0001c0001t0002g0209 a0001c0001t0004g0095 others(5): Show |
8 | HG01243.hp2 HG01257.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.728+4573_728+4581d others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(3): Show |
T | 9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(6): Show |
9 | HG01175.hp2 HG01192.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.728+4572_728+4581d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(4): Show |
T | 30 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(27): Show |
30 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.728+4571_728+4581d others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(8): Show |
T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+4567_728+4581d others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771460 | TAAAAAAA others(12): Show |
T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.728+4563_728+4581d others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116771460 | ||||||
chr12:116771480 | A | T | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.728+4566A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771480 | |||||||
chr12:116771482 | A | T | 6 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 others(3): Show |
6 | HG01074.hp2 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+4568A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771482 | |||||||
chr12:116771484 | A | T | 12 | a0001c0001t0001g0249 a0001c0002t0002g0110 a0001c0002t0005g0151 others(9): Show |
12 | HG01074.hp2 HG01099.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.728+4570A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771484 | |||||||
chr12:116771486 | A | T | 52 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0196 others(49): Show |
52 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.728+4572A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771486 | |||||||
chr12:116771488 | A | AT | 5 | a0001c0001t0001g0086 a0001c0001t0001g0144 a0001c0001t0001g0217 others(2): Show |
5 | HG02293.hp2 HG02300.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+4574_728+4575i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771488 | |||||||
chr12:116771488 | A | T | 130 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0092 others(127): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.728+4574A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771488 | |||||||
chr12:116771490 | A | T | 155 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(152): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.728+4576A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771490 | |||||||
chr12:116771492 | A | T | 172 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(169): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.728+4578A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771492 | |||||||
chr12:116771494 | A | T | 249 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(246): Show |
249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.728+4580A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771494 | |||||||
chr12:116771496 | T | A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.728+4582T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771496 | |||||||
chr12:116771497 | ACG | A | 25 | a0001c0001t0001g0092 a0001c0001t0001g0203 a0001c0001t0001g0216 others(22): Show |
25 | HG01074.hp2 HG01099.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.728+4584_728+4585d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771497 | |||||||
chr12:116771498 | C | T | 152 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(149): Show |
152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.728+4584C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771498 | |||||||
chr12:116771499 | G | A | 152 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(149): Show |
152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.728+4585G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771499 | |||||||
chr12:116771697 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.728+4783A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771697 | |||||||
chr12:116771740 | C | T | 33 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(30): Show |
33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.728+4826C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771740 | |||||||
chr12:116771751 | G | A | 3 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.728+4837G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771751 | |||||||
chr12:116771860 | G | A | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+4946G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116771860 | |||||||
chr12:116772009 | A | G | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+5095A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772009 | |||||||
chr12:116772066 | A | G | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+5152A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772066 | |||||||
chr12:116772082 | T | A | 1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.728+5168T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772082 | |||||||
chr12:116772094 | AT | A | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.728+5189delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116772094 | ||||||
chr12:116772260 | G | A | 177 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(174): Show |
177 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.728+5346G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772260 | |||||||
chr12:116772293 | A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.728+5379A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772293 | |||||||
chr12:116772468 | G | A | 186 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(183): Show |
186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.728+5554G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772468 | |||||||
chr12:116772557 | G | A | 66 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(63): Show |
66 | HG00438.hp2 HG01099.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.728+5643G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772557 | |||||||
chr12:116772625 | T | C | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.728+5711T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772625 | |||||||
chr12:116772834 | C | G | 5 | a0001c0006t0031g0067 a0001c0007t0025g0009 a0001c0007t0025g0057 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.728+5920C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772834 | |||||||
chr12:116772976 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.728+6062A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772976 | |||||||
chr12:116772987 | T | C | 253 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(250): Show |
253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.728+6073T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116772987 | |||||||
chr12:116773003 | A | G | 9 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(6): Show |
9 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.728+6089A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773003 | |||||||
chr12:116773078 | C | T | 1 | a0001c0003t0043g0222 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.729-6117C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773078 | |||||||
chr12:116773214 | G | A | 4 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-5981G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773214 | |||||||
chr12:116773300 | A | G | 33 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(30): Show |
33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.729-5895A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773300 | |||||||
chr12:116773688 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-5507A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116773688 | |||||||
chr12:116774099 | G | A | 187 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(184): Show |
187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.729-5096G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774099 | |||||||
chr12:116774208 | G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4987G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774208 | |||||||
chr12:116774209 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4986T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774209 | |||||||
chr12:116774210 | G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4985G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774210 | |||||||
chr12:116774211 | G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4984G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774211 | |||||||
chr12:116774212 | T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4983T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774212 | |||||||
chr12:116774213 | T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4982T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774213 | |||||||
chr12:116774214 | G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4981G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774214 | |||||||
chr12:116774217 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4978T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774217 | |||||||
chr12:116774219 | G | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4976G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774219 | |||||||
chr12:116774220 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4975T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774220 | |||||||
chr12:116774229 | T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4966T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774229 | |||||||
chr12:116774230 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4965T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774230 | |||||||
chr12:116774232 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4963T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774232 | |||||||
chr12:116774233 | G | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4962G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774233 | |||||||
chr12:116774242 | T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4953T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774242 | |||||||
chr12:116774248 | T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4947T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774248 | |||||||
chr12:116774249 | A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4946A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774249 | |||||||
chr12:116774252 | T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4943T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774252 | |||||||
chr12:116774257 | T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4938T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774257 | |||||||
chr12:116774258 | C | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4937C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774258 | |||||||
chr12:116774259 | A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4936A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774259 | |||||||
chr12:116774260 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4935T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774260 | |||||||
chr12:116774261 | T | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4934T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774261 | |||||||
chr12:116774266 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4929T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774266 | |||||||
chr12:116774268 | T | G | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4927T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774268 | |||||||
chr12:116774270 | C | A | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4925C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774270 | |||||||
chr12:116774271 | G | A | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.729-4924G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774271 | |||||||
chr12:116774276 | A | C | 1 | a0001c0001t0011g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.729-4919A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774276 | |||||||
chr12:116774511 | T | G | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.729-4684T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774511 | |||||||
chr12:116774512 | A | G | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.729-4683A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774512 | |||||||
chr12:116774738 | G | A | 187 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(184): Show |
187 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.729-4457G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774738 | |||||||
chr12:116774770 | C | CGGGTGGA | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0143 others(2): Show |
5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-4407_729-4401d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774770 | ||||||
chr12:116774770 | C | CGGGTGGA others(7): Show |
61 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(58): Show |
61 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.729-4414_729-4401d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774770 | ||||||
chr12:116774773 | GTGGAGGG others(16): Show |
G | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729-4408_729-4386d others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774773 | ||||||
chr12:116774824 | A | T | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729-4371A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774824 | |||||||
chr12:116774871 | A | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 |
3 | HG02976.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.729-4324A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774871 | |||||||
chr12:116774934 | A | AAG | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-4237_729-4236d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | ||||||
chr12:116774934 | A | AAGAG | 3 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0040g0012 |
3 | HG01175.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.729-4239_729-4236d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | ||||||
chr12:116774934 | AAGAGAG | A | 8 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.729-4241_729-4236d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116774934 | ||||||
chr12:116774984 | A | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-4211A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774984 | |||||||
chr12:116774997 | C | T | 4 | a0001c0001t0009g0116 a0001c0001t0009g0130 a0001c0001t0009g0155 others(1): Show |
4 | HG01109.hp2 HG01258.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-4198C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774997 | |||||||
chr12:116774999 | C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-4196C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116774999 | |||||||
chr12:116775261 | C | CA | 150 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(147): Show |
150 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.729-3916dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116775261 | ||||||
chr12:116775278 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-3917A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775278 | |||||||
chr12:116775279 | AGAG | A | 9 | a0001c0002t0005g0163 a0001c0003t0005g0037 a0001c0003t0005g0038 others(6): Show |
9 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.729-3915_729-3913d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775279 | |||||||
chr12:116775294 | C | T | 1 | a0001c0001t0045g0255 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.729-3901C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775294 | |||||||
chr12:116775320 | TGAAGTCA others(3): Show |
T | 250 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(247): Show |
250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.729-3863_729-3854d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116775320 | ||||||
chr12:116775462 | C | T | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729-3733C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775462 | |||||||
chr12:116775713 | C | T | 33 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(30): Show |
33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.729-3482C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775713 | |||||||
chr12:116775722 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.729-3473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775722 | |||||||
chr12:116775795 | C | T | 33 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(30): Show |
33 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.729-3400C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775795 | |||||||
chr12:116775863 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.729-3332C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775863 | |||||||
chr12:116775903 | C | T | 3 | a0001c0002t0005g0149 a0001c0002t0005g0151 a0001c0002t0033g0150 |
3 | HG02922.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.729-3292C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116775903 | |||||||
chr12:116776022 | A | G | 253 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(250): Show |
253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.729-3173A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776022 | |||||||
chr12:116776048 | A | C | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.729-3147A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776048 | |||||||
chr12:116776343 | G | C | 2 | a0001c0007t0025g0057 a0001c0007t0047g0053 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.729-2852G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776343 | |||||||
chr12:116776463 | C | T | 15 | a0001c0002t0018g0022 a0001c0003t0005g0037 a0001c0003t0005g0038 others(12): Show |
15 | HG01243.hp1 HG01891.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.729-2732C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776463 | |||||||
chr12:116776487 | C | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.729-2708C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776487 | |||||||
chr12:116776710 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.729-2485A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776710 | |||||||
chr12:116776812 | G | A | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.729-2383G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776812 | |||||||
chr12:116776916 | A | AT | 30 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0215 others(27): Show |
30 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.729-2260dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | ||||||
chr12:116776916 | A | ATT | 117 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0092 others(114): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.729-2261_729-2260d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | ||||||
chr12:116776916 | A | ATTT | 33 | a0001c0001t0001g0072 a0001c0001t0001g0122 a0001c0001t0001g0164 others(30): Show |
33 | HG01109.hp2 HG01258.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.729-2262_729-2260d others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116776916 | ||||||
chr12:116776986 | C | T | 34 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(31): Show |
34 | HG01175.hp2 HG01243.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.729-2209C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116776986 | |||||||
chr12:116777090 | G | A | 204 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(201): Show |
204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.729-2105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777090 | |||||||
chr12:116777127 | G | A | 5 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0143 others(2): Show |
5 | HG01243.hp2 HG02155.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-2068G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777127 | |||||||
chr12:116777202 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.729-1993G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777202 | |||||||
chr12:116777278 | A | G | 1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.729-1917A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777278 | |||||||
chr12:116777369 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-1826A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777369 | |||||||
chr12:116777543 | T | G | 1 | a0001c0001t0019g0187 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-1652T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777543 | |||||||
chr12:116777647 | G | C | 3 | a0001c0004t0001g0083 a0002c0010t0002g0001 a0002c0010t0002g0002 |
3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.729-1548G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777647 | |||||||
chr12:116777700 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-1495C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777700 | |||||||
chr12:116777715 | C | G | 1 | a0001c0002t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.729-1480C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777715 | |||||||
chr12:116777715 | C | T | 1 | a0001c0001t0041g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.729-1480C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777715 | |||||||
chr12:116777792 | G | T | 1 | a0001c0001t0011g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.729-1403G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116777792 | |||||||
chr12:116778131 | CTCCTTTC others(5): Show |
C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.729-1058_729-1047d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 116778131 | ||||||
chr12:116778328 | C | T | 9 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.729-867C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778328 | |||||||
chr12:116778421 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.729-774A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778421 | |||||||
chr12:116778498 | C | G | 4 | a0001c0004t0001g0083 a0001c0004t0053g0015 a0002c0010t0002g0001 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-697C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778498 | |||||||
chr12:116778798 | C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.729-397C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 6/10 | chr12 | 116778798 | |||||||
chr12:116779407 | A | C | 15 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(12): Show |
15 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.882+59A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779407 | |||||||
chr12:116779543 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+195C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779543 | |||||||
chr12:116779667 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0235 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.882+319G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779667 | |||||||
chr12:116779913 | G | A | 37 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(34): Show |
37 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+565G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779913 | |||||||
chr12:116779915 | C | T | 37 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(34): Show |
37 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+567C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779915 | |||||||
chr12:116779928 | AGACAAGG others(1716): Show |
A | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+581_882+2303de others(1): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116779928 | |||||||
chr12:116780040 | C | T | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+692C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780040 | |||||||
chr12:116780068 | G | C | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+720G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780068 | |||||||
chr12:116780083 | A | T | 1 | a0001c0001t0039g0219 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.882+735A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780083 | |||||||
chr12:116780168 | A | C | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+820A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780168 | |||||||
chr12:116780276 | T | C | 14 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+928T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780276 | |||||||
chr12:116780317 | G | A | 2 | a0001c0001t0003g0146 a0001c0001t0062g0148 |
2 | NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.882+969G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780317 | |||||||
chr12:116780326 | C | A | 1 | a0001c0002t0005g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.882+978C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780326 | |||||||
chr12:116780364 | G | A | 252 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(249): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.882+1016G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780364 | |||||||
chr12:116780472 | G | A | 178 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(175): Show |
178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.882+1124G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780472 | |||||||
chr12:116780593 | C | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+1245C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780593 | |||||||
chr12:116780670 | CA | C | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01169.hp2 HG01243.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.882+1336delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116780670 | ||||||
chr12:116780686 | A | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+1338A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780686 | |||||||
chr12:116780694 | A | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+1346A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780694 | |||||||
chr12:116780723 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.882+1375C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780723 | |||||||
chr12:116780731 | A | G | 1 | a0001c0001t0006g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.882+1383A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780731 | |||||||
chr12:116780908 | C | G | 4 | a0001c0004t0001g0083 a0001c0004t0053g0015 a0002c0010t0002g0001 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1560C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780908 | |||||||
chr12:116780909 | CA | C | 4 | a0001c0004t0001g0083 a0001c0004t0053g0015 a0002c0010t0002g0001 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1562delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116780909 | |||||||
chr12:116781057 | C | T | 199 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(196): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.882+1709C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781057 | |||||||
chr12:116781267 | C | G | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+1919C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781267 | |||||||
chr12:116781279 | G | C | 1 | a0001c0001t0057g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.882+1931G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781279 | |||||||
chr12:116781553 | C | T | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.882+2205C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781553 | |||||||
chr12:116781554 | G | A | 9 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(6): Show |
9 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+2206G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781554 | |||||||
chr12:116781577 | G | A | 4 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2229G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781577 | |||||||
chr12:116781627 | G | A | 2 | a0001c0007t0025g0057 a0001c0007t0047g0053 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+2279G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781627 | |||||||
chr12:116781642 | C | T | 2 | a0001c0001t0004g0183 a0001c0001t0026g0182 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.882+2294C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781642 | |||||||
chr12:116781653 | C | A | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+2305C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781653 | |||||||
chr12:116781654 | T | G | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+2306T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781654 | |||||||
chr12:116781847 | C | T | 184 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(181): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.882+2499C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781847 | |||||||
chr12:116781927 | A | G | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+2579A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781927 | |||||||
chr12:116781934 | C | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2586C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781934 | |||||||
chr12:116781935 | T | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2587T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781935 | |||||||
chr12:116781948 | A | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+2600A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781948 | |||||||
chr12:116781951 | C | T | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+2603C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116781951 | |||||||
chr12:116782047 | C | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0223 a0002c0010t0002g0254 |
3 | HG00609.hp2 HG02040.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.882+2699C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782047 | |||||||
chr12:116782056 | G | T | 1 | a0001c0001t0072g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882+2708G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782056 | |||||||
chr12:116782066 | G | A | 4 | a0001c0004t0001g0083 a0001c0004t0053g0015 a0002c0010t0002g0001 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2718G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782066 | |||||||
chr12:116782073 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+2725C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782073 | |||||||
chr12:116782074 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.882+2726G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782074 | |||||||
chr12:116782079 | C | CAAAAAAA | 13 | a0001c0001t0001g0202 a0001c0002t0018g0022 a0001c0003t0005g0037 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+2740_882+2746d others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0004g0177 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+2739_882+2746d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(2): Show |
29 | a0001c0001t0001g0171 a0001c0001t0002g0032 a0001c0001t0004g0095 others(26): Show |
29 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+2738_882+2746d others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0007g0170 a0001c0002t0001g0076 a0001c0002t0004g0005 others(5): Show |
8 | HG02486.hp1 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+2737_882+2746d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(4): Show |
2 | a0001c0002t0005g0003 a0001c0002t0068g0042 |
2 | HG01175.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.882+2736_882+2746d others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(8): Show |
3 | a0001c0002t0001g0079 a0001c0004t0001g0083 a0002c0010t0002g0002 |
3 | HG01099.hp2 HG02132.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+2732_882+2746d others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(9): Show |
17 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0215 others(14): Show |
17 | HG01258.hp1 HG01975.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(10): Show |
10 | a0001c0001t0001g0193 a0001c0001t0001g0235 a0001c0001t0002g0189 others(7): Show |
10 | HG00438.hp2 HG01257.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(11): Show |
1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.882+2746_882+2747i others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0211 a0001c0001t0007g0087 a0001c0001t0039g0219 others(2): Show |
5 | HG00408.hp1 HG00423.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(13): Show |
31 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(28): Show |
31 | HG00609.hp1 HG01261.hp1 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(14): Show |
67 | a0001c0001t0001g0069 a0001c0001t0001g0119 a0001c0001t0001g0138 others(64): Show |
67 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(15): Show |
30 | a0001c0001t0001g0094 a0001c0001t0001g0196 a0001c0001t0001g0206 others(27): Show |
30 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(16): Show |
16 | a0001c0001t0001g0195 a0001c0001t0001g0257 a0001c0001t0001g0259 others(13): Show |
16 | HG01106.hp2 HG01891.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.882+2746_882+2747i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0205 a0001c0001t0019g0124 a0001c0001t0057g0220 |
3 | HG00140.hp1 HG02055.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(18): Show |
1 | a0001c0003t0002g0101 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(19): Show |
2 | a0001c0003t0002g0100 a0001c0003t0002g0102 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(24): Show |
2 | a0001c0001t0019g0153 a0001c0016t0032g0044 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(33): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(27): Show |
2 | a0001c0001t0019g0187 a0001c0001t0058g0188 |
2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+2746_882+2747i others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782079 | C | CAAAAAAA others(30): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(39): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782079 | ||||||
chr12:116782081 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.882+2746_882+2747i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116782081 | ||||||
chr12:116782142 | G | A | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.882+2794G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782142 | |||||||
chr12:116782148 | G | A | 6 | a0001c0006t0031g0067 a0001c0007t0025g0009 a0001c0007t0025g0057 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+2800G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782148 | |||||||
chr12:116782184 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2836A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782184 | |||||||
chr12:116782252 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+2904C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782252 | |||||||
chr12:116782343 | G | A | 2 | a0001c0001t0004g0185 a0001c0001t0048g0241 |
2 | HG02074.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.882+2995G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782343 | |||||||
chr12:116782431 | A | C | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882+3083A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782431 | |||||||
chr12:116782454 | G | C | 178 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(175): Show |
178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.882+3106G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782454 | |||||||
chr12:116782601 | C | T | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3253C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782601 | |||||||
chr12:116782716 | G | A | 4 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+3368G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782716 | |||||||
chr12:116782762 | A | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+3414A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782762 | |||||||
chr12:116782798 | T | C | 2 | a0001c0001t0001g0168 a0001c0004t0012g0137 |
2 | HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.882+3450T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782798 | |||||||
chr12:116782971 | A | G | 3 | a0001c0004t0001g0083 a0002c0010t0002g0001 a0002c0010t0002g0002 |
3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+3623A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116782971 | |||||||
chr12:116783033 | T | A | 1 | a0001c0002t0012g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.882+3685T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783033 | |||||||
chr12:116783043 | A | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3695A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783043 | |||||||
chr12:116783055 | T | C | 12 | a0001c0001t0001g0164 a0001c0001t0002g0236 a0001c0001t0006g0115 others(9): Show |
12 | HG01109.hp2 HG01258.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+3707T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783055 | |||||||
chr12:116783121 | G | A | 6 | a0001c0001t0005g0104 a0001c0005t0013g0006 a0001c0005t0013g0186 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+3773G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783121 | |||||||
chr12:116783179 | T | A | 1 | a0001c0001t0049g0184 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882+3831T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783179 | |||||||
chr12:116783187 | T | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+3839T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783187 | |||||||
chr12:116783323 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0235 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.882+3975C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783323 | |||||||
chr12:116783453 | G | A | 1 | a0001c0001t0014g0158 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.882+4105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783453 | |||||||
chr12:116783692 | T | C | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+4344T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783692 | |||||||
chr12:116783839 | G | T | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+4491G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783839 | |||||||
chr12:116783947 | G | A | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+4599G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783947 | |||||||
chr12:116783980 | G | A | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+4632G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783980 | |||||||
chr12:116783984 | T | C | 1 | a0001c0006t0006g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882+4636T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116783984 | |||||||
chr12:116784173 | G | C | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4825G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784173 | |||||||
chr12:116784323 | C | T | 2 | a0001c0001t0001g0237 a0001c0002t0012g0089 |
2 | HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.882+4975C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784323 | |||||||
chr12:116784335 | C | T | 7 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
7 | HG00741.hp1 HG01074.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+4987C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784335 | |||||||
chr12:116784360 | G | A | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+5012G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784360 | |||||||
chr12:116784485 | A | G | 2 | a0001c0001t0019g0187 a0001c0001t0058g0188 |
2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+5137A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784485 | |||||||
chr12:116784493 | T | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+5145T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784493 | |||||||
chr12:116784651 | C | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+5303C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784651 | |||||||
chr12:116784673 | T | C | 1 | a0001c0001t0010g0233 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.882+5325T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784673 | |||||||
chr12:116784752 | A | G | 1 | a0001c0001t0049g0184 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.882+5404A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116784752 | |||||||
chr12:116785130 | A | G | 1 | a0001c0004t0002g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+5782A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785130 | |||||||
chr12:116785249 | C | CTGTG | 3 | a0001c0001t0001g0216 a0001c0001t0003g0131 a0001c0008t0003g0207 |
3 | HG02273.hp1 NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.882+5924_882+5927d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTG | 6 | a0001c0001t0002g0032 a0001c0001t0003g0085 a0001c0001t0008g0026 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5922_882+5927d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(1): Show |
125 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(122): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.882+5920_882+5927d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(3): Show |
23 | a0001c0001t0001g0168 a0001c0001t0001g0206 a0001c0001t0001g0249 others(20): Show |
23 | HG00673.hp1 HG01099.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.882+5918_882+5927d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0027g0125 a0001c0002t0005g0003 |
2 | HG01175.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.882+5916_882+5927d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0002g0031 a0001c0002t0063g0173 |
2 | HG01169.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.882+5914_882+5927d others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(9): Show |
3 | a0001c0002t0005g0062 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.882+5912_882+5927d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(13): Show |
1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.882+5908_882+5927d others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(15): Show |
1 | a0001c0007t0034g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882+5906_882+5927d others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(17): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+5904_882+5927d others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(19): Show |
1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+5902_882+5927d others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | C | CTGTGTGT others(23): Show |
1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+5927_882+5928i others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | CTG | C | 4 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5926_882+5927d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785249 | CTGTG | C | 5 | a0001c0003t0035g0088 a0001c0007t0025g0009 a0001c0007t0025g0057 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+5924_882+5927d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785249 | ||||||
chr12:116785275 | G | GTGTGTGT others(2): Show |
34 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(31): Show |
34 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(4): Show |
17 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(14): Show |
17 | HG02074.hp1 HG02257.hp1 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(6): Show |
4 | a0001c0001t0004g0096 a0001c0001t0004g0167 a0001c0001t0004g0185 others(1): Show |
4 | HG02965.hp1 HG03225.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(8): Show |
6 | a0001c0001t0004g0143 a0001c0003t0005g0037 a0001c0003t0005g0038 others(3): Show |
6 | HG00741.hp1 HG02155.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(10): Show |
5 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0002t0050g0004 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(12): Show |
5 | a0001c0001t0004g0095 a0001c0002t0004g0005 a0001c0005t0020g0161 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+5927_882+5928i others(21): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(14): Show |
1 | a0001c0001t0019g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882+5927_882+5928i others(23): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(16): Show |
1 | a0001c0001t0057g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.882+5927_882+5928i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(18): Show |
2 | a0001c0001t0019g0187 a0001c0001t0058g0188 |
2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+5927_882+5928i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785275 | G | GTGTGTGT others(20): Show |
1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+5927_882+5928i others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785275 | |||||||
chr12:116785277 | C | G | 77 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(74): Show |
77 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+5929C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785277 | |||||||
chr12:116785278 | G | C | 77 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(74): Show |
77 | HG00140.hp1 HG00438.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+5930G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785278 | |||||||
chr12:116785286 | G | T | 1 | a0001c0007t0034g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.882+5938G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785286 | |||||||
chr12:116785293 | G | GTTTGTTT others(3): Show |
71 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(68): Show |
71 | HG00438.hp2 HG01099.hp2 HG01243.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+5953_882+5962d others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785293 | ||||||
chr12:116785293 | G | GTTTGTTT others(13): Show |
4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+5962_882+5963i others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116785293 | ||||||
chr12:116785504 | T | C | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6156T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785504 | |||||||
chr12:116785551 | C | A | 1 | a0001c0002t0002g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.882+6203C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785551 | |||||||
chr12:116785567 | T | C | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+6219T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785567 | |||||||
chr12:116785751 | G | A | 4 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+6403G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785751 | |||||||
chr12:116785836 | T | C | 256 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(253): Show |
256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.882+6488T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785836 | |||||||
chr12:116785843 | G | A | 2 | a0001c0001t0007g0070 a0001c0001t0007g0174 |
2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.882+6495G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785843 | |||||||
chr12:116785851 | C | T | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+6503C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785851 | |||||||
chr12:116785910 | T | C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+6562T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785910 | |||||||
chr12:116785972 | A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+6624A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116785972 | |||||||
chr12:116786032 | A | G | 1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+6684A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786032 | |||||||
chr12:116786122 | C | CT | 30 | a0001c0001t0001g0171 a0001c0001t0001g0202 a0001c0001t0001g0243 others(27): Show |
30 | HG01884.hp2 HG02074.hp1 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.882+6790dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116786122 | ||||||
chr12:116786268 | C | T | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+6920C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786268 | |||||||
chr12:116786286 | TA | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6940delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116786286 | ||||||
chr12:116786331 | G | A | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.882+6983G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786331 | |||||||
chr12:116786352 | C | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+7004C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786352 | |||||||
chr12:116786362 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+7014C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786362 | |||||||
chr12:116786388 | G | T | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+7040G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786388 | |||||||
chr12:116786544 | A | AT | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+7196_882+7197i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786544 | |||||||
chr12:116786548 | T | G | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+7200T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786548 | |||||||
chr12:116786563 | G | A | 28 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(25): Show |
28 | HG00438.hp2 HG01099.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7215G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786563 | |||||||
chr12:116786575 | C | A | 1 | a0001c0001t0003g0160 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+7227C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786575 | |||||||
chr12:116786693 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+7345C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786693 | |||||||
chr12:116786754 | G | T | 152 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(149): Show |
152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.882+7406G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786754 | |||||||
chr12:116786811 | C | T | 3 | a0001c0004t0001g0083 a0002c0010t0002g0001 a0002c0010t0002g0002 |
3 | HG02132.hp2 HG02135.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.882+7463C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786811 | |||||||
chr12:116786984 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0232 |
2 | NA18941.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.882+7636G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116786984 | |||||||
chr12:116787035 | G | A | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+7687G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787035 | |||||||
chr12:116787054 | G | A | 9 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+7706G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787054 | |||||||
chr12:116787078 | T | C | 1 | a0001c0002t0021g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+7730T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787078 | |||||||
chr12:116787118 | G | A | 254 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(251): Show |
254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.882+7770G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787118 | |||||||
chr12:116787273 | C | T | 70 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(67): Show |
70 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.882+7925C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787273 | |||||||
chr12:116787394 | G | A | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+8046G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787394 | |||||||
chr12:116787686 | C | T | 33 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(30): Show |
33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+8338C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787686 | |||||||
chr12:116787718 | GA | G | 183 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(180): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.882+8385delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116787718 | ||||||
chr12:116787718 | GAA | G | 44 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(41): Show |
44 | HG00140.hp1 HG00438.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+8384_882+8385d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116787718 | ||||||
chr12:116787838 | T | A | 3 | a0001c0001t0017g0175 a0001c0001t0017g0200 a0001c0001t0017g0213 |
3 | NA18945.hp1 NA18954.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.882+8490T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787838 | |||||||
chr12:116787914 | C | T | 7 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 others(4): Show |
7 | HG00741.hp1 HG01074.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+8566C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787914 | |||||||
chr12:116787984 | A | G | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.882+8636A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116787984 | |||||||
chr12:116788133 | G | A | 2 | a0001c0007t0025g0057 a0001c0007t0047g0053 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+8785G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788133 | |||||||
chr12:116788223 | A | G | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+8875A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788223 | |||||||
chr12:116788254 | C | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+8906C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788254 | |||||||
chr12:116788255 | G | A | 6 | a0001c0006t0031g0067 a0001c0007t0025g0009 a0001c0007t0025g0057 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+8907G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788255 | |||||||
chr12:116788528 | C | T | 2 | a0001c0001t0001g0069 a0001c0002t0001g0251 |
2 | HG02080.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.882+9180C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788528 | |||||||
chr12:116788666 | G | C | 1 | a0001c0003t0002g0101 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.882+9318G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788666 | |||||||
chr12:116788767 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+9419A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788767 | |||||||
chr12:116788796 | T | C | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+9448T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116788796 | |||||||
chr12:116788810 | T | TGGTGGAT others(17): Show |
1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+9464_882+9487d others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788810 | ||||||
chr12:116788826 | A | AGATGGAT others(5): Show |
30 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(27): Show |
30 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+9490_882+9501d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | ||||||
chr12:116788826 | A | AGATGGAT others(9): Show |
11 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0008g0140 others(8): Show |
11 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+9486_882+9501d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | ||||||
chr12:116788826 | A | AGATGGAT others(13): Show |
4 | a0001c0002t0018g0022 a0001c0005t0030g0051 a0001c0005t0030g0052 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9482_882+9501d others(22): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | ||||||
chr12:116788826 | AGATG | A | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.882+9498_882+9501d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788826 | ||||||
chr12:116788955 | GGGAT | G | 198 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(195): Show |
198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.882+9634_882+9637d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | ||||||
chr12:116788955 | GGGATGGA others(1): Show |
G | 7 | a0001c0001t0017g0175 a0001c0001t0017g0200 a0001c0001t0017g0213 others(4): Show |
7 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+9630_882+9637d others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | ||||||
chr12:116788955 | GGGATGGA others(5): Show |
G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+9626_882+9637d others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | ||||||
chr12:116788955 | GGGATGGA others(9): Show |
G | 2 | a0001c0001t0015g0112 a0001c0001t0024g0126 |
2 | HG00673.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.882+9622_882+9637d others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788955 | ||||||
chr12:116788968 | GGATGGAT others(32): Show |
G | 1 | a0001c0001t0002g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+9634_882+9672d others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116788968 | ||||||
chr12:116789106 | G | A | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+9758G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789106 | |||||||
chr12:116789163 | A | AGATGGGT others(69): Show |
4 | a0001c0004t0001g0083 a0001c0004t0053g0015 a0002c0010t0002g0001 others(1): Show |
4 | HG02132.hp2 HG02135.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9837_882+9912d others(78): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789163 | ||||||
chr12:116789228 | G | A | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+9880G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789228 | |||||||
chr12:116789247 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+9899G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789247 | |||||||
chr12:116789311 | G | A | 1 | a0001c0002t0005g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+9963G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789311 | |||||||
chr12:116789369 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+10021G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789369 | |||||||
chr12:116789389 | A | G | 4 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+10041A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789389 | |||||||
chr12:116789438 | GTAGA | G | 8 | a0001c0003t0005g0037 a0001c0003t0005g0038 a0001c0003t0016g0035 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+10092_882+1009 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789438 | ||||||
chr12:116789440 | A | AGATG | 25 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(22): Show |
25 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+10114_882+1011 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789440 | ||||||
chr12:116789458 | ATGGATGG others(24): Show |
A | 1 | a0001c0001t0004g0185 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.882+10175_882+1020 others(35): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789458 | ||||||
chr12:116789635 | G | GTGGA | 8 | a0001c0001t0002g0236 a0001c0001t0004g0172 a0001c0001t0007g0169 others(5): Show |
8 | HG01074.hp2 HG01261.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+10317_882+1032 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | ||||||
chr12:116789635 | G | GTGGATGG others(1): Show |
10 | a0001c0001t0004g0109 a0001c0001t0004g0143 a0001c0002t0018g0022 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+10313_882+1032 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | ||||||
chr12:116789635 | G | GTGGATGG others(5): Show |
30 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0166 others(27): Show |
30 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+10309_882+1032 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | ||||||
chr12:116789635 | G | GTGGATGG others(9): Show |
2 | a0001c0001t0004g0096 a0001c0002t0001g0076 |
2 | HG03225.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.882+10305_882+1032 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | ||||||
chr12:116789635 | GTGGA | G | 15 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(12): Show |
15 | HG00140.hp1 HG01175.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+10317_882+1032 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789635 | ||||||
chr12:116789722 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+10374T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789722 | |||||||
chr12:116789772 | ATGGATGG others(16): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.882+10457_882+1047 others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789772 | ||||||
chr12:116789824 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882+10476G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789824 | |||||||
chr12:116789876 | G | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+10528G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789876 | |||||||
chr12:116789938 | T | C | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+10590T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116789938 | |||||||
chr12:116789960 | G | GTGGA | 39 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0215 others(36): Show |
39 | HG00438.hp2 HG01175.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.882+10642_882+1064 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | ||||||
chr12:116789960 | G | GTGGATGG others(1): Show |
148 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(145): Show |
148 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.882+10638_882+1064 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | ||||||
chr12:116789960 | G | GTGGATGG others(5): Show |
43 | a0001c0001t0001g0171 a0001c0001t0001g0216 a0001c0001t0001g0217 others(40): Show |
43 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.882+10634_882+1064 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | ||||||
chr12:116789960 | G | GTGGATGG others(9): Show |
1 | a0001c0001t0001g0259 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.882+10630_882+1064 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116789960 | ||||||
chr12:116790171 | T | C | 1 | a0001c0002t0001g0076 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.882+10823T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790171 | |||||||
chr12:116790334 | A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+10986A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790334 | |||||||
chr12:116790373 | T | TG | 49 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(46): Show |
49 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+11026dupG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116790373 | ||||||
chr12:116790376 | G | A | 2 | a0001c0001t0014g0027 a0001c0009t0023g0028 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.882+11028G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790376 | |||||||
chr12:116790538 | G | A | 1 | a0001c0001t0062g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.882+11190G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790538 | |||||||
chr12:116790653 | C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+11305C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790653 | |||||||
chr12:116790654 | G | A | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+11306G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790654 | |||||||
chr12:116790681 | G | C | 1 | a0001c0019t0002g0267 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.882+11333G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790681 | |||||||
chr12:116790748 | G | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0259 |
2 | HG01978.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.882+11400G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790748 | |||||||
chr12:116790756 | A | G | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+11408A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790756 | |||||||
chr12:116790771 | A | G | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.882+11423A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790771 | |||||||
chr12:116790799 | T | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+11451T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790799 | |||||||
chr12:116790814 | G | A | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+11466G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116790814 | |||||||
chr12:116791334 | G | A | 1 | a0001c0013t0013g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+11986G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791334 | |||||||
chr12:116791529 | G | C | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12181G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791529 | |||||||
chr12:116791734 | G | A | 245 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(242): Show |
245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.882+12386G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791734 | |||||||
chr12:116791786 | A | G | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+12438A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791786 | |||||||
chr12:116791793 | G | T | 245 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(242): Show |
245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.882+12445G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791793 | |||||||
chr12:116791814 | A | AATCCTAT others(13): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+12468_882+1248 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116791814 | ||||||
chr12:116791839 | A | T | 27 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+12491A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791839 | |||||||
chr12:116791972 | A | G | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+12624A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116791972 | |||||||
chr12:116792015 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+12667G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792015 | |||||||
chr12:116792179 | A | G | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.882+12831A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792179 | |||||||
chr12:116792236 | GACGGGGT others(48): Show |
G | 1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+12889_882+1294 others(59): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792236 | |||||||
chr12:116792238 | C | A | 3 | a0001c0002t0005g0003 a0001c0002t0005g0062 a0001c0011t0040g0012 |
3 | HG01175.hp2 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.882+12890C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792238 | |||||||
chr12:116792262 | C | G | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12914C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792262 | |||||||
chr12:116792308 | C | T | 4 | a0001c0002t0018g0022 a0001c0005t0030g0051 a0001c0005t0030g0052 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+12960C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792308 | |||||||
chr12:116792342 | G | A | 45 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(42): Show |
45 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+12994G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792342 | |||||||
chr12:116792525 | A | G | 251 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(248): Show |
251 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.882+13177A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792525 | |||||||
chr12:116792550 | A | T | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882+13202A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792550 | |||||||
chr12:116792589 | C | T | 1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+13241C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792589 | |||||||
chr12:116792614 | C | T | 33 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(30): Show |
33 | HG01243.hp2 HG02055.hp1 HG02074.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+13266C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792614 | |||||||
chr12:116792846 | C | T | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+13498C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116792846 | |||||||
chr12:116793071 | G | C | 4 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+13723G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793071 | |||||||
chr12:116793210 | C | CT | 147 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(144): Show |
147 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.882+13881dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | ||||||
chr12:116793210 | C | CTT | 14 | a0001c0001t0001g0197 a0001c0001t0017g0213 a0001c0001t0022g0225 others(11): Show |
14 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+13880_882+1388 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | ||||||
chr12:116793210 | CT | C | 25 | a0001c0001t0002g0032 a0001c0001t0007g0174 a0001c0001t0008g0026 others(22): Show |
25 | HG00140.hp1 HG01243.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+13881delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | ||||||
chr12:116793210 | CTT | C | 26 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(23): Show |
26 | HG00438.hp2 HG01099.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+13880_882+1388 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116793210 | ||||||
chr12:116793248 | C | A | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882+13900C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793248 | |||||||
chr12:116793442 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+14094C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793442 | |||||||
chr12:116793468 | G | A | 54 | a0001c0001t0001g0171 a0001c0001t0002g0031 a0001c0001t0002g0045 others(51): Show |
54 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+14120G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793468 | |||||||
chr12:116793636 | G | A | 51 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(48): Show |
51 | HG00438.hp1 HG00544.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.882+14288G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793636 | |||||||
chr12:116793640 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.882+14292T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793640 | |||||||
chr12:116793800 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.882+14452C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116793800 | |||||||
chr12:116794041 | G | A | 3 | a0001c0002t0005g0003 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG01175.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+14693G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794041 | |||||||
chr12:116794130 | T | G | 20 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(17): Show |
20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+14782T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794130 | |||||||
chr12:116794338 | TTGTAATC others(801): Show |
T | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+15019_882+1582 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794338 | ||||||
chr12:116794489 | G | A | 117 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(114): Show |
117 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.882+15141G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794489 | |||||||
chr12:116794490 | C | T | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15142C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794490 | |||||||
chr12:116794495 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0015g0176 |
2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.882+15147G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794495 | |||||||
chr12:116794521 | C | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15173C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794521 | |||||||
chr12:116794523 | G | A | 1 | a0001c0001t0072g0120 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.882+15175G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794523 | |||||||
chr12:116794542 | G | A | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.882+15194G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794542 | |||||||
chr12:116794547 | G | A | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+15199G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794547 | |||||||
chr12:116794587 | G | T | 1 | a0001c0001t0003g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.882+15239G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794587 | |||||||
chr12:116794646 | A | AGAAG | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+15312_882+1531 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | ||||||
chr12:116794646 | A | AGGAGGGA others(17): Show |
2 | a0001c0004t0001g0083 a0001c0006t0051g0013 |
2 | HG00741.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.882+15299_882+1530 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | ||||||
chr12:116794646 | A | AGGAGGGA others(17): Show |
1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.882+15299_882+1530 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | ||||||
chr12:116794646 | A | AGGAGGGA others(21): Show |
3 | a0001c0001t0002g0210 a0002c0010t0002g0001 a0002c0010t0002g0002 |
3 | HG00438.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.882+15299_882+1530 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | ||||||
chr12:116794646 | AGAAG | A | 4 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15312_882+1531 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794646 | ||||||
chr12:116794648 | A | G | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15300A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794648 | |||||||
chr12:116794652 | A | G | 4 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15304A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794652 | |||||||
chr12:116794656 | A | AAGGGAGG others(13): Show |
1 | a0001c0001t0014g0158 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.882+15311_882+1531 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | ||||||
chr12:116794656 | A | AAGGGAGG others(9): Show |
6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+15311_882+1531 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | ||||||
chr12:116794656 | A | AAGGGAGG others(13): Show |
2 | a0001c0005t0013g0006 a0001c0013t0013g0046 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+15311_882+1531 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | ||||||
chr12:116794656 | A | AAGGGAGG others(17): Show |
3 | a0001c0005t0013g0186 a0001c0013t0013g0159 a0001c0018t0056g0058 |
3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.882+15311_882+1531 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | ||||||
chr12:116794656 | AAGGAAGG others(13): Show |
A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15312_882+1533 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794656 | ||||||
chr12:116794660 | A | G | 13 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(10): Show |
13 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+15312A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794660 | |||||||
chr12:116794664 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15316G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794664 | |||||||
chr12:116794668 | A | AAGGGAGG others(9): Show |
1 | a0001c0002t0015g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.882+15323_882+1532 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(13): Show |
111 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(108): Show |
111 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(17): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0217 a0001c0001t0003g0131 |
3 | HG02293.hp2 HG02300.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.882+15323_882+1532 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(5): Show |
1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+15323_882+1532 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(9): Show |
5 | a0001c0003t0014g0063 a0001c0005t0030g0051 a0001c0005t0030g0052 others(2): Show |
5 | HG01891.hp1 HG02965.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(13): Show |
9 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+15323_882+1532 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | AAGGGAGG others(21): Show |
2 | a0001c0007t0025g0057 a0001c0007t0047g0053 |
2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+15323_882+1532 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794668 | ||||||
chr12:116794668 | A | G | 21 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(18): Show |
21 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.882+15320A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794668 | |||||||
chr12:116794672 | A | AAGGGAGG others(5): Show |
4 | a0001c0001t0004g0172 a0001c0001t0004g0183 a0001c0001t0026g0182 others(1): Show |
4 | HG02809.hp1 HG03831.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+15334_882+1534 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | AAGGGAGG others(9): Show |
20 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(17): Show |
20 | HG00140.hp2 HG01106.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.882+15330_882+1534 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | AAGGGAGG others(13): Show |
51 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(48): Show |
51 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.882+15326_882+1534 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | AAGGGAGG others(17): Show |
12 | a0001c0001t0005g0104 a0001c0002t0004g0005 a0001c0002t0005g0062 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(28): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | AAGGGAGG others(21): Show |
11 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(8): Show |
11 | HG02074.hp1 HG02683.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | AAGGGAGG others(25): Show |
4 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0087 others(1): Show |
4 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15345_882+1534 others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794672 | ||||||
chr12:116794672 | A | G | 153 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(150): Show |
153 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.882+15324A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794672 | |||||||
chr12:116794674 | G | GGAA | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15327_882+1532 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794674 | ||||||
chr12:116794674 | G | GGGAGGGA others(19): Show |
1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15345_882+1534 others(30): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794674 | ||||||
chr12:116794678 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15330G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794678 | |||||||
chr12:116794682 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15334G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794682 | |||||||
chr12:116794686 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15338G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794686 | |||||||
chr12:116794690 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15342G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794690 | |||||||
chr12:116794697 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15349G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794697 | |||||||
chr12:116794698 | AAGGG | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+15354_882+1535 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116794698 | ||||||
chr12:116794699 | A | G | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15351A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794699 | |||||||
chr12:116794702 | G | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+15354G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794702 | |||||||
chr12:116794708 | A | G | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+15360A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794708 | |||||||
chr12:116794806 | C | T | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+15458C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794806 | |||||||
chr12:116794853 | G | T | 2 | a0001c0005t0030g0051 a0001c0005t0030g0052 |
2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.882+15505G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794853 | |||||||
chr12:116794961 | A | C | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15613A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116794961 | |||||||
chr12:116795009 | A | T | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.882+15661A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795009 | |||||||
chr12:116795029 | A | G | 7 | a0001c0001t0003g0085 a0001c0001t0003g0146 a0001c0001t0003g0191 others(4): Show |
7 | HG02040.hp2 NA18954.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+15681A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795029 | |||||||
chr12:116795115 | G | GA | 4 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+15771dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116795115 | ||||||
chr12:116795302 | A | G | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+15954A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795302 | |||||||
chr12:116795387 | G | A | 1 | a0001c0001t0061g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.882+16039G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795387 | |||||||
chr12:116795410 | G | GA | 21 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(18): Show |
21 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(18): Show |
intron_variant | MODIFIER | c.882+16075dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116795410 | ||||||
chr12:116795484 | T | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+16136T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795484 | |||||||
chr12:116795564 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.882+16216G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795564 | |||||||
chr12:116795711 | T | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+16363T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795711 | |||||||
chr12:116795740 | A | G | 2 | a0001c0003t0035g0088 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+16392A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795740 | |||||||
chr12:116795785 | G | A | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+16437G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116795785 | |||||||
chr12:116796053 | C | T | 1 | a0001c0002t0002g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+16705C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796053 | |||||||
chr12:116796095 | G | GT | 5 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0002c0010t0002g0001 others(2): Show |
5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+16747_882+1674 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796095 | |||||||
chr12:116796125 | T | C | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+16777T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796125 | |||||||
chr12:116796136 | C | T | 7 | a0001c0001t0002g0210 a0001c0001t0004g0109 a0001c0004t0001g0083 others(4): Show |
7 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+16788C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796136 | |||||||
chr12:116796268 | A | G | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+16920A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796268 | |||||||
chr12:116796501 | A | G | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+17153A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796501 | |||||||
chr12:116796687 | C | T | 20 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(17): Show |
20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.882+17339C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796687 | |||||||
chr12:116796719 | G | A | 1 | a0001c0001t0048g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.882+17371G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796719 | |||||||
chr12:116796719 | G | T | 139 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(136): Show |
139 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.882+17371G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796719 | |||||||
chr12:116796785 | T | G | 25 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(22): Show |
25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+17437T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796785 | |||||||
chr12:116796851 | G | A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+17503G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796851 | |||||||
chr12:116796871 | G | T | 249 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(246): Show |
249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.882+17523G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796871 | |||||||
chr12:116796894 | G | C | 5 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+17546G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796894 | |||||||
chr12:116796985 | C | T | 139 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(136): Show |
139 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.882+17637C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116796985 | |||||||
chr12:116797048 | T | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+17700T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797048 | |||||||
chr12:116797053 | T | A | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+17705T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797053 | |||||||
chr12:116797218 | G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+17870G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797218 | |||||||
chr12:116797224 | C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+17876C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797224 | |||||||
chr12:116797266 | G | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+17918G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797266 | |||||||
chr12:116797297 | T | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+17949T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797297 | |||||||
chr12:116797357 | C | T | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.882+18009C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797357 | |||||||
chr12:116797428 | C | T | 25 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(22): Show |
25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+18080C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797428 | |||||||
chr12:116797454 | G | A | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+18106G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797454 | |||||||
chr12:116797483 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+18135C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797483 | |||||||
chr12:116797530 | G | A | 6 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+18182G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797530 | |||||||
chr12:116797535 | T | G | 85 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(82): Show |
85 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.882+18187T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797535 | |||||||
chr12:116797538 | C | CA | 25 | a0001c0001t0002g0210 a0001c0001t0005g0104 a0001c0001t0019g0124 others(22): Show |
25 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+18205dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797538 | ||||||
chr12:116797538 | CA | C | 7 | a0001c0001t0001g0262 a0001c0001t0007g0174 a0001c0001t0027g0121 others(4): Show |
7 | HG01257.hp1 HG02523.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+18205delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797538 | ||||||
chr12:116797644 | G | GAA | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+18297_882+1829 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797644 | ||||||
chr12:116797700 | C | T | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+18352C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797700 | |||||||
chr12:116797701 | G | A | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+18353G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797701 | |||||||
chr12:116797729 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18381G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797729 | |||||||
chr12:116797735 | ACTC | A | 33 | a0001c0001t0003g0085 a0001c0001t0003g0106 a0001c0001t0003g0117 others(30): Show |
33 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.882+18390_882+1839 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797735 | ||||||
chr12:116797809 | A | C | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18461A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797809 | |||||||
chr12:116797816 | A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+18468A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797816 | |||||||
chr12:116797843 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.882+18495T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797843 | |||||||
chr12:116797872 | C | CTTTTGGG others(43): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+18573_882+1857 others(54): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116797872 | ||||||
chr12:116797893 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+18545G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797893 | |||||||
chr12:116797922 | T | G | 255 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(252): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.882+18574T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797922 | |||||||
chr12:116797955 | C | T | 24 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0045 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+18607C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797955 | |||||||
chr12:116797959 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+18611T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116797959 | |||||||
chr12:116798031 | G | C | 24 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0045 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+18683G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798031 | |||||||
chr12:116798064 | A | G | 1 | a0001c0002t0015g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.882+18716A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798064 | |||||||
chr12:116798076 | C | T | 93 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(90): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.882+18728C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798076 | |||||||
chr12:116798212 | C | T | 1 | a0001c0007t0025g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+18864C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798212 | |||||||
chr12:116798225 | C | CA | 46 | a0001c0001t0001g0171 a0001c0001t0002g0031 a0001c0001t0002g0032 others(43): Show |
46 | HG00544.hp1 HG01884.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.882+18889dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116798225 | ||||||
chr12:116798225 | CA | C | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+18889delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116798225 | ||||||
chr12:116798239 | A | C | 6 | a0001c0001t0007g0070 a0001c0002t0005g0003 a0001c0009t0023g0028 others(3): Show |
6 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+18891A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798239 | |||||||
chr12:116798331 | G | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+18983G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798331 | |||||||
chr12:116798360 | A | T | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+19012A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798360 | |||||||
chr12:116798548 | C | G | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+19200C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798548 | |||||||
chr12:116798585 | A | T | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19237A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798585 | |||||||
chr12:116798742 | A | G | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19394A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798742 | |||||||
chr12:116798765 | G | A | 1 | a0001c0002t0002g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+19417G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798765 | |||||||
chr12:116798777 | T | C | 1 | a0001c0001t0004g0167 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+19429T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798777 | |||||||
chr12:116798796 | G | A | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+19448G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798796 | |||||||
chr12:116798886 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.882+19538C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116798886 | |||||||
chr12:116799099 | C | T | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+19751C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799099 | |||||||
chr12:116799134 | C | T | 138 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(135): Show |
138 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.882+19786C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799134 | |||||||
chr12:116799204 | C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+19856C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799204 | |||||||
chr12:116799209 | C | A | 2 | a0001c0003t0035g0088 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+19861C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799209 | |||||||
chr12:116799326 | G | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+19978G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799326 | |||||||
chr12:116799503 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.882+20155A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799503 | |||||||
chr12:116799505 | C | T | 2 | a0001c0002t0002g0265 a0001c0002t0010g0266 |
2 | NA18945.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.882+20157C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799505 | |||||||
chr12:116799579 | G | GT | 44 | a0001c0001t0002g0210 a0001c0001t0003g0085 a0001c0001t0003g0106 others(41): Show |
44 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+20240dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116799579 | ||||||
chr12:116799701 | C | T | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+20353C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799701 | |||||||
chr12:116799751 | C | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 |
3 | HG02976.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.882+20403C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799751 | |||||||
chr12:116799806 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.882+20458A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799806 | |||||||
chr12:116799987 | A | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+20639A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116799987 | |||||||
chr12:116800127 | C | T | 117 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(114): Show |
117 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.882+20779C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800127 | |||||||
chr12:116800169 | C | A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+20821C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800169 | |||||||
chr12:116800171 | A | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+20823A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800171 | |||||||
chr12:116800180 | G | A | 244 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(241): Show |
244 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.882+20832G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800180 | |||||||
chr12:116800236 | C | T | 3 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+20888C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800236 | |||||||
chr12:116800355 | G | A | 72 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(69): Show |
72 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.882+21007G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800355 | |||||||
chr12:116800526 | G | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+21178G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800526 | |||||||
chr12:116800583 | G | A | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.882+21235G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800583 | |||||||
chr12:116800633 | C | CA | 6 | a0001c0002t0001g0082 a0001c0003t0014g0063 a0001c0005t0020g0161 others(3): Show |
6 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+21297dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800633 | ||||||
chr12:116800633 | CA | C | 151 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(148): Show |
151 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.882+21297delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800633 | ||||||
chr12:116800711 | G | T | 1 | a0001c0002t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.882+21363G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800711 | |||||||
chr12:116800738 | T | C | 18 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(15): Show |
18 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+21390T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800738 | |||||||
chr12:116800773 | C | T | 1 | a0001c0011t0040g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+21425C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800773 | |||||||
chr12:116800775 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.882+21427T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800775 | |||||||
chr12:116800812 | T | TCAAAATA others(163): Show |
1 | a0001c0009t0023g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+21464_882+2146 others(174): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800812 | |||||||
chr12:116800812 | T | TCAAAATA others(233): Show |
1 | a0001c0011t0040g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+21464_882+2146 others(244): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800812 | |||||||
chr12:116800812 | T | TTAAAA | 47 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0001g0122 others(44): Show |
47 | HG00140.hp1 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.882+21510_882+2151 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | T | TTAAAATA others(3): Show |
53 | a0001c0001t0001g0119 a0001c0001t0001g0198 a0001c0001t0001g0203 others(50): Show |
53 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.882+21505_882+2151 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | T | TTAAAATA others(8): Show |
36 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0094 others(33): Show |
36 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.882+21500_882+2151 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | T | TTAAAATA others(13): Show |
4 | a0001c0001t0001g0195 a0001c0001t0002g0236 a0001c0001t0022g0225 others(1): Show |
4 | HG01106.hp2 HG01261.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+21495_882+2151 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | T | TTAAAATA others(18): Show |
3 | a0001c0001t0001g0202 a0001c0001t0001g0224 a0001c0001t0041g0145 |
3 | NA18956.hp1 NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.882+21490_882+2151 others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | TTAAAA | T | 21 | a0001c0001t0002g0036 a0001c0001t0014g0039 a0001c0001t0046g0114 others(18): Show |
21 | HG01358.hp1 HG01891.hp1 HG02922.hp1 others(18): Show |
intron_variant | MODIFIER | c.882+21510_882+2151 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | TTAAAATA others(3): Show |
T | 4 | a0001c0001t0004g0143 a0001c0002t0002g0129 a0001c0014t0018g0019 others(1): Show |
4 | HG01106.hp1 HG02155.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+21505_882+2151 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | TTAAAATA others(8): Show |
T | 4 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0002t0004g0005 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+21500_882+2151 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800812 | TTAAAATA others(13): Show |
T | 2 | a0001c0003t0035g0088 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.882+21495_882+2151 others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800812 | ||||||
chr12:116800813 | T | C | 8 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(5): Show |
8 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+21465T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800813 | |||||||
chr12:116800853 | TAAAATAA | T | 4 | a0001c0004t0001g0083 a0001c0006t0051g0013 a0002c0010t0002g0001 others(1): Show |
4 | HG00741.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+21509_882+2151 others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800853 | ||||||
chr12:116800858 | T | TAAAATAA others(258): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.882+21514_882+2151 others(269): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800858 | ||||||
chr12:116800860 | A | AAATAAAA others(6): Show |
1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.882+21514_882+2151 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800860 | ||||||
chr12:116800861 | A | AATAAAAT others(73): Show |
1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.882+21514_882+2151 others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116800861 | ||||||
chr12:116800863 | A | T | 10 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(7): Show |
10 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+21515A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800863 | |||||||
chr12:116800870 | A | G | 256 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(253): Show |
256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.882+21522A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116800870 | |||||||
chr12:116801084 | G | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.882+21736G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801084 | |||||||
chr12:116801214 | T | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+21866T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801214 | |||||||
chr12:116801345 | C | G | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+21997C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801345 | |||||||
chr12:116801429 | A | C | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+22081A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801429 | |||||||
chr12:116801481 | C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+22133C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801481 | |||||||
chr12:116801804 | T | TTTTG | 8 | a0001c0001t0002g0032 a0001c0001t0003g0240 a0001c0001t0008g0030 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+22484_882+2248 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | ||||||
chr12:116801804 | TTTTG | T | 104 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(101): Show |
104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.882+22484_882+2248 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | ||||||
chr12:116801804 | TTTTGTTT others(1): Show |
T | 9 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+22480_882+2248 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116801804 | ||||||
chr12:116801836 | T | G | 22 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0045 others(19): Show |
22 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.882+22488T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801836 | |||||||
chr12:116801907 | C | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+22559C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801907 | |||||||
chr12:116801982 | C | T | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+22634C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116801982 | |||||||
chr12:116802074 | G | A | 10 | a0001c0001t0005g0104 a0001c0002t0005g0062 a0001c0003t0005g0037 others(7): Show |
10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+22726G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802074 | |||||||
chr12:116802110 | T | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+22762T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802110 | |||||||
chr12:116802211 | A | G | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+22863A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802211 | |||||||
chr12:116802307 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.882+22959G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802307 | |||||||
chr12:116802388 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0244 |
2 | HG02080.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.882+23040T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802388 | |||||||
chr12:116802404 | C | T | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+23056C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802404 | |||||||
chr12:116802552 | A | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+23204A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802552 | |||||||
chr12:116802603 | G | C | 2 | a0001c0001t0002g0210 a0002c0010t0002g0254 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.882+23255G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802603 | |||||||
chr12:116802821 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+23473G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802821 | |||||||
chr12:116802872 | A | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+23524A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802872 | |||||||
chr12:116802910 | C | G | 1 | a0001c0001t0041g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.882+23562C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802910 | |||||||
chr12:116802932 | C | CA | 54 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.882+23597dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116802932 | ||||||
chr12:116802958 | G | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.882+23610G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116802958 | |||||||
chr12:116803006 | A | G | 115 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(112): Show |
115 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.882+23658A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803006 | |||||||
chr12:116803075 | A | T | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23727A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803075 | |||||||
chr12:116803076 | C | T | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23728C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803076 | |||||||
chr12:116803077 | A | T | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23729A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803077 | |||||||
chr12:116803078 | G | A | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.882+23730G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803078 | |||||||
chr12:116803094 | TA | T | 156 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(153): Show |
156 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.882+23757delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116803094 | ||||||
chr12:116803177 | G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+23829G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803177 | |||||||
chr12:116803229 | G | A | 3 | a0001c0003t0035g0088 a0001c0009t0052g0016 a0001c0011t0054g0011 |
3 | HG02809.hp1 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+23881G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803229 | |||||||
chr12:116803253 | C | T | 3 | a0001c0001t0057g0220 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG00140.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.882+23905C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803253 | |||||||
chr12:116803411 | T | C | 247 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(244): Show |
247 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.882+24063T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803411 | |||||||
chr12:116803707 | C | A | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+24359C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803707 | |||||||
chr12:116803709 | C | T | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+24361C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803709 | |||||||
chr12:116803752 | A | G | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+24404A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803752 | |||||||
chr12:116803980 | G | C | 1 | a0001c0004t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.882+24632G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116803980 | |||||||
chr12:116804073 | C | G | 255 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(252): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.882+24725C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804073 | |||||||
chr12:116804084 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.882+24736G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804084 | |||||||
chr12:116804260 | A | G | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+24912A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804260 | |||||||
chr12:116804478 | T | C | 11 | a0001c0001t0002g0210 a0001c0002t0005g0003 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+25130T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804478 | |||||||
chr12:116804598 | A | G | 1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.882+25250A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804598 | |||||||
chr12:116804868 | G | A | 25 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(22): Show |
25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.882+25520G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804868 | |||||||
chr12:116804926 | C | T | 12 | a0001c0001t0011g0099 a0001c0001t0011g0157 a0001c0001t0014g0039 others(9): Show |
12 | HG01074.hp2 HG01109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+25578C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116804926 | |||||||
chr12:116805005 | A | G | 3 | a0001c0001t0003g0127 a0001c0001t0003g0162 a0001c0001t0003g0242 |
3 | HG00423.hp2 HG02155.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.882+25657A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805005 | |||||||
chr12:116805121 | C | CT | 143 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(140): Show |
143 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.882+25789dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | ||||||
chr12:116805121 | C | CTT | 92 | a0001c0001t0001g0141 a0001c0001t0001g0171 a0001c0001t0001g0190 others(89): Show |
92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.882+25788_882+2578 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | ||||||
chr12:116805121 | C | CTTT | 7 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(4): Show |
7 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+25787_882+2578 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116805121 | ||||||
chr12:116805245 | A | G | 1 | a0001c0004t0069g0024 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.882+25897A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805245 | |||||||
chr12:116805418 | A | C | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26070A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805418 | |||||||
chr12:116805464 | A | G | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+26116A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805464 | |||||||
chr12:116805489 | T | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0217 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.882+26141T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805489 | |||||||
chr12:116805501 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.882+26153G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805501 | |||||||
chr12:116805531 | G | A | 207 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(204): Show |
207 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.882+26183G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805531 | |||||||
chr12:116805582 | C | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26234C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805582 | |||||||
chr12:116805870 | G | C | 1 | a0001c0002t0033g0150 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.882+26522G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805870 | |||||||
chr12:116805932 | A | G | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26584A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805932 | |||||||
chr12:116805938 | A | G | 204 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(201): Show |
204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.882+26590A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116805938 | |||||||
chr12:116806003 | C | T | 8 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+26655C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806003 | |||||||
chr12:116806022 | T | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+26674T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806022 | |||||||
chr12:116806047 | C | T | 2 | a0001c0001t0003g0199 a0001c0004t0029g0055 |
2 | HG02738.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.882+26699C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806047 | |||||||
chr12:116806094 | A | G | 1 | a0001c0012t0001g0239 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.882+26746A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806094 | |||||||
chr12:116806147 | G | A | 36 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(33): Show |
36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.882+26799G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806147 | |||||||
chr12:116806237 | G | A | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.882+26889G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806237 | |||||||
chr12:116806367 | CA | C | 57 | a0001c0001t0001g0122 a0001c0001t0001g0164 a0001c0001t0001g0168 others(54): Show |
57 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.882+27034delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | ||||||
chr12:116806367 | CAA | C | 7 | a0001c0001t0001g0216 a0001c0001t0019g0187 a0001c0001t0057g0220 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | ||||||
chr12:116806367 | CAAA | C | 13 | a0001c0001t0004g0096 a0001c0001t0004g0109 a0001c0001t0004g0172 others(10): Show |
13 | HG01175.hp2 HG02074.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+27032_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | ||||||
chr12:116806367 | CAAAAA | C | 9 | a0001c0001t0001g0195 a0001c0001t0001g0203 a0001c0001t0001g0206 others(6): Show |
9 | HG01106.hp2 HG01192.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+27030_882+2703 others(9): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806367 | ||||||
chr12:116806376 | AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0001g0208 a0001c0001t0015g0112 |
2 | HG00673.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.882+27030_882+2704 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806376 | ||||||
chr12:116806377 | A | AT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0197 a0001c0001t0001g0202 others(4): Show |
7 | HG00544.hp2 HG00609.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+27029_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | |||||||
chr12:116806377 | A | ATAT | 33 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+27029_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | |||||||
chr12:116806377 | A | T | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.882+27029A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806377 | |||||||
chr12:116806378 | AAAAATAT | A | 7 | a0001c0001t0001g0171 a0001c0001t0004g0185 a0001c0001t0007g0070 others(4): Show |
7 | HG02523.hp2 NA18948.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+27032_882+2703 others(11): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806378 | ||||||
chr12:116806379 | A | AT | 6 | a0001c0001t0003g0106 a0001c0001t0004g0143 a0001c0001t0004g0166 others(3): Show |
6 | HG02071.hp2 HG02155.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27031_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | |||||||
chr12:116806379 | A | ATAT | 14 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0253 others(11): Show |
14 | HG00423.hp2 HG00621.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+27031_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | |||||||
chr12:116806379 | A | T | 56 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.882+27031A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806379 | |||||||
chr12:116806381 | A | AAAT | 11 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(8): Show |
11 | HG02145.hp1 HG02572.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+27034_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806381 | ||||||
chr12:116806381 | A | AATAT | 6 | a0001c0002t0042g0077 a0001c0003t0006g0204 a0001c0003t0006g0229 others(3): Show |
6 | HG03490.hp1 HG03654.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27049_882+2705 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806381 | ||||||
chr12:116806381 | A | AT | 9 | a0001c0001t0001g0141 a0001c0001t0001g0235 a0001c0001t0002g0133 others(6): Show |
9 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | |||||||
chr12:116806381 | A | ATAT | 25 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0215 others(22): Show |
25 | HG00438.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+27033_882+2703 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | |||||||
chr12:116806381 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.882+27033A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | |||||||
chr12:116806381 | A | T | 108 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(105): Show |
108 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.882+27033A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806381 | |||||||
chr12:116806382 | AT | A | 6 | a0001c0001t0005g0104 a0001c0003t0005g0038 a0001c0006t0005g0017 others(3): Show |
6 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+27035delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806382 | |||||||
chr12:116806383 | T | A | 4 | a0001c0001t0008g0041 a0001c0002t0008g0140 a0001c0005t0030g0051 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+27035T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806383 | |||||||
chr12:116806385 | T | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0260 a0001c0001t0004g0095 others(1): Show |
4 | HG02647.hp2 HG03710.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+27037T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806385 | |||||||
chr12:116806389 | T | G | 68 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(65): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.882+27041T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806389 | |||||||
chr12:116806389 | T | TAG | 3 | a0001c0001t0002g0023 a0001c0001t0019g0124 a0001c0016t0032g0044 |
3 | HG01192.hp2 HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.882+27042_882+2704 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | ||||||
chr12:116806389 | T | TAGATAG | 9 | a0001c0001t0002g0133 a0001c0001t0010g0233 a0001c0001t0011g0099 others(6): Show |
9 | HG00408.hp2 HG02109.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+27042_882+2704 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | ||||||
chr12:116806389 | T | TAGATAGA others(3): Show |
2 | a0001c0001t0001g0197 a0001c0004t0012g0137 |
2 | HG00544.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.882+27042_882+2704 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806389 | ||||||
chr12:116806393 | T | G | 159 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(156): Show |
159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.882+27045T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806393 | |||||||
chr12:116806393 | T | TAG | 3 | a0001c0005t0013g0006 a0001c0006t0051g0013 a0001c0007t0025g0009 |
3 | HG00741.hp1 HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+27046_882+2704 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | ||||||
chr12:116806393 | T | TAGATAG | 10 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0001g0202 others(7): Show |
10 | HG00438.hp1 HG00609.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+27046_882+2704 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | ||||||
chr12:116806393 | T | TAGATAGA others(3): Show |
1 | a0001c0001t0002g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+27046_882+2704 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806393 | ||||||
chr12:116806395 | TATATAG | T | 3 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0008g0140 |
3 | HG03041.hp2 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882+27051_882+2705 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806395 | ||||||
chr12:116806397 | T | G | 233 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(230): Show |
233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.882+27049T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806397 | |||||||
chr12:116806397 | T | TATAGATA others(1): Show |
4 | a0001c0001t0002g0031 a0001c0001t0002g0048 a0001c0005t0030g0051 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+27076_882+2708 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806397 | ||||||
chr12:116806397 | T | TATAGATA others(5): Show |
2 | a0001c0001t0002g0045 a0001c0009t0037g0043 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.882+27072_882+2708 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806397 | ||||||
chr12:116806401 | G | T | 4 | a0001c0001t0001g0208 a0001c0001t0015g0112 a0001c0003t0006g0054 others(1): Show |
4 | HG00140.hp2 HG00673.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+27053G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806401 | |||||||
chr12:116806588 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.883-27204A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806588 | |||||||
chr12:116806671 | A | G | 239 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(236): Show |
239 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.883-27121A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806671 | |||||||
chr12:116806741 | C | G | 54 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-27051C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116806741 | |||||||
chr12:116806745 | C | CA | 61 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0190 others(58): Show |
61 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-27030dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806745 | ||||||
chr12:116806745 | CA | C | 11 | a0001c0001t0001g0202 a0001c0001t0002g0048 a0001c0001t0008g0041 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.883-27030delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116806745 | ||||||
chr12:116807153 | C | T | 11 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(8): Show |
11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-26639C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807153 | |||||||
chr12:116807229 | G | A | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-26563G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807229 | |||||||
chr12:116807341 | G | A | 204 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(201): Show |
204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.883-26451G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807341 | |||||||
chr12:116807368 | G | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-26424G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807368 | |||||||
chr12:116807520 | C | T | 5 | a0001c0002t0002g0129 a0001c0004t0002g0025 a0001c0004t0069g0024 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-26272C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807520 | |||||||
chr12:116807567 | A | T | 5 | a0001c0002t0002g0129 a0001c0004t0002g0025 a0001c0004t0069g0024 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-26225A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807567 | |||||||
chr12:116807657 | T | A | 54 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-26135T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807657 | |||||||
chr12:116807828 | G | C | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.883-25964G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807828 | |||||||
chr12:116807855 | GT | G | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25936delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807855 | |||||||
chr12:116807906 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25886C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807906 | |||||||
chr12:116807999 | G | A | 1 | a0001c0003t0016g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.883-25793G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116807999 | |||||||
chr12:116808019 | A | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25773A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808019 | |||||||
chr12:116808021 | G | T | 54 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-25771G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808021 | |||||||
chr12:116808031 | C | T | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25761C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808031 | |||||||
chr12:116808049 | C | T | 11 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(8): Show |
11 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-25743C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808049 | |||||||
chr12:116808050 | G | A | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-25742G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808050 | |||||||
chr12:116808228 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25564G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808228 | |||||||
chr12:116808234 | G | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-25558G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808234 | |||||||
chr12:116808236 | A | G | 250 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(247): Show |
250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.883-25556A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808236 | |||||||
chr12:116808586 | G | C | 204 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(201): Show |
204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.883-25206G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808586 | |||||||
chr12:116808608 | C | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-25184C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808608 | |||||||
chr12:116808636 | A | G | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-25156A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808636 | |||||||
chr12:116808718 | A | G | 1 | a0001c0002t0067g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-25074A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808718 | |||||||
chr12:116808831 | G | C | 54 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(51): Show |
54 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-24961G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116808831 | |||||||
chr12:116809051 | A | G | 3 | a0001c0001t0003g0085 a0001c0001t0003g0212 a0001c0001t0029g0227 |
3 | NA18954.hp1 NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.883-24741A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809051 | |||||||
chr12:116809187 | GTTCA | G | 69 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(66): Show |
69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.883-24571_883-2456 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116809187 | ||||||
chr12:116809187 | GTTCATTC others(1): Show |
G | 178 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(175): Show |
178 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.883-24575_883-2456 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116809187 | ||||||
chr12:116809231 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24561G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809231 | |||||||
chr12:116809337 | G | A | 11 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(8): Show |
11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-24455G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809337 | |||||||
chr12:116809369 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24423G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809369 | |||||||
chr12:116809377 | C | T | 5 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-24415C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809377 | |||||||
chr12:116809584 | C | T | 7 | a0001c0001t0008g0041 a0001c0002t0002g0129 a0001c0002t0008g0140 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-24208C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809584 | |||||||
chr12:116809619 | A | G | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-24173A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809619 | |||||||
chr12:116809656 | C | T | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0051g0013 others(3): Show |
6 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-24136C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809656 | |||||||
chr12:116809750 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-24042G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809750 | |||||||
chr12:116809803 | G | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-23989G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809803 | |||||||
chr12:116809858 | A | G | 9 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0002t0005g0149 others(6): Show |
9 | HG02109.hp1 HG02145.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-23934A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809858 | |||||||
chr12:116809981 | G | T | 117 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(114): Show |
117 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.883-23811G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809981 | |||||||
chr12:116809987 | C | T | 2 | a0001c0001t0008g0041 a0001c0002t0008g0140 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-23805C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116809987 | |||||||
chr12:116810318 | C | G | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-23474C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810318 | |||||||
chr12:116810322 | A | G | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.883-23470A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810322 | |||||||
chr12:116810388 | C | T | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-23404C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810388 | |||||||
chr12:116810555 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-23237G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810555 | |||||||
chr12:116810828 | G | C | 3 | a0001c0001t0001g0164 a0001c0002t0001g0111 a0001c0002t0012g0014 |
3 | HG01361.hp1 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.883-22964G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810828 | |||||||
chr12:116810831 | G | A | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-22961G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810831 | |||||||
chr12:116810934 | G | A | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-22858G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810934 | |||||||
chr12:116810985 | T | C | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG01192.hp1 HG01257.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-22807T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116810985 | |||||||
chr12:116811074 | A | G | 248 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(245): Show |
248 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-22718A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811074 | |||||||
chr12:116811132 | G | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-22660G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811132 | |||||||
chr12:116811196 | A | C | 1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.883-22596A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811196 | |||||||
chr12:116811373 | A | AT | 184 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(181): Show |
184 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.883-22408dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116811373 | ||||||
chr12:116811373 | A | ATT | 46 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.883-22409_883-2240 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116811373 | ||||||
chr12:116811435 | G | A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-22357G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811435 | |||||||
chr12:116811444 | C | T | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-22348C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811444 | |||||||
chr12:116811573 | G | A | 5 | a0001c0001t0005g0245 a0001c0002t0005g0003 a0001c0009t0023g0028 others(2): Show |
5 | HG01175.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-22219G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811573 | |||||||
chr12:116811623 | G | T | 2 | a0001c0001t0008g0041 a0001c0002t0008g0140 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-22169G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811623 | |||||||
chr12:116811650 | A | G | 25 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(22): Show |
25 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-22142A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811650 | |||||||
chr12:116811679 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0237 a0001c0002t0012g0089 |
3 | HG01074.hp1 HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.883-22113G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811679 | |||||||
chr12:116811687 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-22105G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811687 | |||||||
chr12:116811759 | T | C | 11 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(8): Show |
11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-22033T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811759 | |||||||
chr12:116811813 | G | A | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-21979G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811813 | |||||||
chr12:116811874 | A | G | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-21918A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116811874 | |||||||
chr12:116812076 | G | A | 3 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-21716G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812076 | |||||||
chr12:116812229 | C | T | 194 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(191): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.883-21563C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812229 | |||||||
chr12:116812478 | A | G | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-21314A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812478 | |||||||
chr12:116812596 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-21196G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812596 | |||||||
chr12:116812604 | A | G | 195 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(192): Show |
195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.883-21188A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812604 | |||||||
chr12:116812647 | G | A | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-21145G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812647 | |||||||
chr12:116812670 | G | A | 1 | a0001c0002t0067g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-21122G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812670 | |||||||
chr12:116812825 | C | T | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-20967C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812825 | |||||||
chr12:116812883 | G | A | 194 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(191): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.883-20909G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812883 | |||||||
chr12:116812893 | C | T | 20 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(17): Show |
20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-20899C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812893 | |||||||
chr12:116812929 | T | C | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-20863T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812929 | |||||||
chr12:116812979 | A | G | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-20813A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116812979 | |||||||
chr12:116813024 | C | T | 4 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-20768C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813024 | |||||||
chr12:116813037 | C | G | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-20755C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813037 | |||||||
chr12:116813125 | T | G | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-20667T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813125 | |||||||
chr12:116813147 | C | T | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-20645C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813147 | |||||||
chr12:116813728 | G | A | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-20064G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813728 | |||||||
chr12:116813805 | C | T | 248 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(245): Show |
248 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-19987C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116813805 | |||||||
chr12:116814080 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-19712C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814080 | |||||||
chr12:116814081 | G | A | 1 | a0001c0001t0004g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.883-19711G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814081 | |||||||
chr12:116814083 | G | T | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-19709G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814083 | |||||||
chr12:116814126 | C | T | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.883-19666C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814126 | |||||||
chr12:116814185 | C | A | 6 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(3): Show |
6 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-19607C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814185 | |||||||
chr12:116814248 | C | T | 7 | a0001c0001t0001g0171 a0001c0001t0007g0070 a0001c0001t0007g0071 others(4): Show |
7 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-19544C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814248 | |||||||
chr12:116814249 | A | C | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-19543A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814249 | |||||||
chr12:116814683 | T | A | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-19109T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814683 | |||||||
chr12:116814688 | T | C | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-19104T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814688 | |||||||
chr12:116814694 | G | A | 5 | a0001c0001t0003g0106 a0001c0001t0003g0131 a0001c0001t0004g0128 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-19098G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814694 | |||||||
chr12:116814747 | C | T | 34 | a0001c0001t0003g0085 a0001c0001t0003g0106 a0001c0001t0003g0117 others(31): Show |
34 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.883-19045C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814747 | |||||||
chr12:116814823 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.883-18969C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814823 | |||||||
chr12:116814835 | T | C | 198 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(195): Show |
198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.883-18957T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814835 | |||||||
chr12:116814950 | G | A | 6 | a0001c0001t0001g0195 a0001c0002t0005g0003 a0001c0009t0023g0028 others(3): Show |
6 | HG01106.hp2 HG01175.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-18842G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116814950 | |||||||
chr12:116815306 | G | A | 7 | a0001c0001t0006g0115 a0001c0001t0009g0116 a0001c0001t0009g0118 others(4): Show |
7 | HG01109.hp2 HG01258.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-18486G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815306 | |||||||
chr12:116815395 | C | T | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-18397C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815395 | |||||||
chr12:116815447 | G | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0235 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.883-18345G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815447 | |||||||
chr12:116815554 | T | C | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-18238T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815554 | |||||||
chr12:116815648 | C | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-18144C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815648 | |||||||
chr12:116815859 | CCAGCAGG others(1): Show |
C | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-17929_883-1792 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116815859 | ||||||
chr12:116815915 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.883-17877T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116815915 | |||||||
chr12:116816066 | T | A | 199 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(196): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.883-17726T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816066 | |||||||
chr12:116816174 | C | G | 133 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(130): Show |
133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.883-17618C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816174 | |||||||
chr12:116816366 | C | A | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-17426C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816366 | |||||||
chr12:116816436 | A | G | 14 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-17356A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816436 | |||||||
chr12:116816447 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-17345C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816447 | |||||||
chr12:116816448 | G | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-17344G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816448 | |||||||
chr12:116816469 | G | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-17323G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816469 | |||||||
chr12:116816643 | A | C | 11 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(8): Show |
11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-17149A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816643 | |||||||
chr12:116816669 | A | G | 20 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0166 others(17): Show |
20 | HG00544.hp1 HG02074.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-17123A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816669 | |||||||
chr12:116816672 | T | C | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-17120T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816672 | |||||||
chr12:116816675 | T | G | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-17117T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816675 | |||||||
chr12:116816836 | TAAC | T | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-16953_883-1695 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116816836 | ||||||
chr12:116816860 | T | A | 3 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 |
3 | HG02572.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.883-16932T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116816860 | |||||||
chr12:116817115 | C | T | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-16677C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817115 | |||||||
chr12:116817159 | C | T | 133 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(130): Show |
133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.883-16633C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817159 | |||||||
chr12:116817276 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883-16516G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817276 | |||||||
chr12:116817495 | G | A | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.883-16297G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817495 | |||||||
chr12:116817633 | T | A | 11 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(8): Show |
11 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-16159T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817633 | |||||||
chr12:116817710 | T | C | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-16082T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817710 | |||||||
chr12:116817850 | C | G | 133 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(130): Show |
133 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.883-15942C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817850 | |||||||
chr12:116817896 | C | A | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.883-15896C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817896 | |||||||
chr12:116817992 | G | A | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-15800G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116817992 | |||||||
chr12:116818228 | G | C | 1 | a0001c0001t0010g0226 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.883-15564G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818228 | |||||||
chr12:116818298 | G | C | 5 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-15494G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818298 | |||||||
chr12:116818320 | C | CA | 186 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(183): Show |
186 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.883-15456dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | ||||||
chr12:116818320 | C | CAA | 22 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0195 others(19): Show |
22 | HG00140.hp1 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-15457_883-1545 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | ||||||
chr12:116818320 | C | CAAA | 44 | a0001c0001t0001g0141 a0001c0001t0001g0235 a0001c0001t0002g0133 others(41): Show |
44 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.883-15458_883-1545 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116818320 | ||||||
chr12:116818363 | C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-15429C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818363 | |||||||
chr12:116818553 | G | A | 35 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(32): Show |
35 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.883-15239G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818553 | |||||||
chr12:116818557 | G | C | 1 | a0001c0001t0002g0236 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.883-15235G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818557 | |||||||
chr12:116818893 | A | C | 199 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(196): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.883-14899A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818893 | |||||||
chr12:116818895 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.883-14897A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116818895 | |||||||
chr12:116819160 | G | T | 3 | a0001c0005t0013g0186 a0001c0013t0013g0159 a0001c0018t0056g0058 |
3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883-14632G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819160 | |||||||
chr12:116819207 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.883-14585G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819207 | |||||||
chr12:116819214 | C | T | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-14578C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819214 | |||||||
chr12:116819372 | C | G | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.883-14420C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819372 | |||||||
chr12:116819381 | C | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-14411C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819381 | |||||||
chr12:116819393 | C | A | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-14399C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819393 | |||||||
chr12:116819430 | C | G | 1 | a0001c0002t0042g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.883-14362C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819430 | |||||||
chr12:116819448 | G | T | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.883-14344G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819448 | |||||||
chr12:116819664 | C | G | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-14128C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819664 | |||||||
chr12:116819737 | C | A | 2 | a0001c0001t0003g0146 a0001c0001t0062g0148 |
2 | NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.883-14055C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819737 | |||||||
chr12:116819739 | T | G | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-14053T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819739 | |||||||
chr12:116819871 | T | G | 199 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(196): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.883-13921T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819871 | |||||||
chr12:116819927 | A | G | 50 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(47): Show |
50 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-13865A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819927 | |||||||
chr12:116819947 | T | C | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.883-13845T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819947 | |||||||
chr12:116819948 | A | G | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.883-13844A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116819948 | |||||||
chr12:116820052 | T | C | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-13740T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820052 | |||||||
chr12:116820240 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.883-13552G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820240 | |||||||
chr12:116820288 | C | G | 149 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(146): Show |
149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.883-13504C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820288 | |||||||
chr12:116820342 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.883-13450G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820342 | |||||||
chr12:116820373 | T | C | 248 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(245): Show |
248 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-13419T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820373 | |||||||
chr12:116820615 | C | T | 1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-13177C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820615 | |||||||
chr12:116820631 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-13161C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820631 | |||||||
chr12:116820901 | A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-12891A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116820901 | |||||||
chr12:116821032 | A | G | 2 | a0001c0002t0004g0268 a0001c0009t0037g0043 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.883-12760A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821032 | |||||||
chr12:116821051 | G | T | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-12741G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821051 | |||||||
chr12:116821058 | C | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-12734C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821058 | |||||||
chr12:116821073 | G | C | 1 | a0001c0002t0001g0076 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.883-12719G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821073 | |||||||
chr12:116821088 | G | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-12704G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821088 | |||||||
chr12:116821175 | C | G | 29 | a0001c0001t0001g0171 a0001c0001t0004g0166 a0001c0001t0004g0167 others(26): Show |
29 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.883-12617C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821175 | |||||||
chr12:116821230 | C | T | 8 | a0001c0001t0008g0041 a0001c0001t0046g0114 a0001c0002t0002g0129 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-12562C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821230 | |||||||
chr12:116821319 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821319 | |||||||
chr12:116821403 | G | A | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-12389G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821403 | |||||||
chr12:116821471 | C | G | 229 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(226): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.883-12321C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821471 | |||||||
chr12:116821540 | G | A | 4 | a0001c0002t0063g0173 a0001c0002t0064g0263 a0001c0002t0065g0093 others(1): Show |
4 | HG01169.hp2 HG01884.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-12252G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821540 | |||||||
chr12:116821546 | T | C | 5 | a0001c0002t0005g0003 a0001c0009t0023g0028 a0001c0011t0023g0007 others(2): Show |
5 | HG01175.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12246T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821546 | |||||||
chr12:116821572 | A | C | 255 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(252): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.883-12220A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821572 | |||||||
chr12:116821639 | G | A | 5 | a0001c0001t0004g0109 a0001c0001t0004g0166 a0001c0001t0004g0167 others(2): Show |
5 | HG02683.hp2 HG03688.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-12153G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821639 | |||||||
chr12:116821671 | G | A | 1 | a0001c0001t0041g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.883-12121G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821671 | |||||||
chr12:116821741 | C | T | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-12051C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821741 | |||||||
chr12:116821802 | C | CT | 6 | a0001c0001t0002g0045 a0001c0001t0004g0109 a0001c0001t0007g0174 others(3): Show |
6 | HG01243.hp2 HG02523.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-11958dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821802 | C | CTT | 10 | a0001c0001t0002g0032 a0001c0001t0008g0030 a0001c0001t0011g0033 others(7): Show |
10 | HG00673.hp1 HG01106.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-11959_883-1195 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821802 | CT | C | 53 | a0001c0001t0001g0069 a0001c0001t0001g0206 a0001c0001t0001g0244 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.883-11958delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821802 | CTT | C | 106 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(103): Show |
106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.883-11959_883-1195 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821802 | CTTT | C | 57 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(54): Show |
57 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.883-11960_883-1195 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821802 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0075 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.883-11967_883-1195 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821802 | ||||||
chr12:116821863 | C | CTGGAGTG others(2): Show |
56 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(53): Show |
56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.883-11910_883-1190 others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821863 | ||||||
chr12:116821863 | CTGGAGTG others(2): Show |
C | 6 | a0001c0001t0002g0236 a0001c0002t0005g0003 a0001c0009t0023g0028 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-11910_883-1190 others(13): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116821863 | ||||||
chr12:116821930 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.883-11862G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116821930 | |||||||
chr12:116822169 | C | G | 116 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(113): Show |
116 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.883-11623C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822169 | |||||||
chr12:116822332 | C | G | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-11460C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822332 | |||||||
chr12:116822467 | G | A | 2 | a0001c0009t0037g0043 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.883-11325G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822467 | |||||||
chr12:116822707 | TAGAA | T | 14 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(11): Show |
14 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-11081_883-1107 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116822707 | ||||||
chr12:116822731 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-11061G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822731 | |||||||
chr12:116822854 | A | G | 31 | a0001c0001t0002g0032 a0001c0001t0002g0210 a0001c0001t0008g0026 others(28): Show |
31 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.883-10938A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822854 | |||||||
chr12:116822934 | T | C | 15 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(12): Show |
15 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-10858T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116822934 | |||||||
chr12:116823041 | A | G | 11 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-10751A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823041 | |||||||
chr12:116823192 | G | C | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-10600G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823192 | |||||||
chr12:116823237 | C | T | 2 | a0001c0009t0052g0016 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.883-10555C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823237 | |||||||
chr12:116823264 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.883-10528C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823264 | |||||||
chr12:116823512 | T | C | 173 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(170): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.883-10280T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823512 | |||||||
chr12:116823687 | A | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-10105A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823687 | |||||||
chr12:116823901 | AT | A | 4 | a0001c0006t0005g0017 a0001c0007t0005g0060 a0001c0007t0016g0059 others(1): Show |
4 | HG01243.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-9887delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116823901 | ||||||
chr12:116823912 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0224 |
2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.883-9880G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116823912 | |||||||
chr12:116824319 | C | T | 14 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(11): Show |
14 | HG01106.hp1 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-9473C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824319 | |||||||
chr12:116824362 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-9430G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824362 | |||||||
chr12:116824369 | A | G | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-9423A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824369 | |||||||
chr12:116824476 | C | T | 3 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-9316C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824476 | |||||||
chr12:116824482 | T | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-9310T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824482 | |||||||
chr12:116824564 | A | C | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-9228A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824564 | |||||||
chr12:116824655 | C | T | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-9137C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824655 | |||||||
chr12:116824741 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-9051C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824741 | |||||||
chr12:116824965 | A | G | 9 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0002t0005g0003 others(6): Show |
9 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-8827A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116824965 | |||||||
chr12:116825008 | G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-8784G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825008 | |||||||
chr12:116825032 | A | T | 4 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-8760A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825032 | |||||||
chr12:116825164 | T | C | 52 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(49): Show |
52 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.883-8628T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825164 | |||||||
chr12:116825208 | A | G | 1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.883-8584A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825208 | |||||||
chr12:116825650 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.883-8142C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825650 | |||||||
chr12:116825678 | A | G | 1 | a0001c0003t0002g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-8114A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825678 | |||||||
chr12:116825755 | G | A | 67 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.883-8037G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825755 | |||||||
chr12:116825797 | T | C | 1 | a0001c0013t0013g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883-7995T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825797 | |||||||
chr12:116825880 | G | A | 1 | a0001c0002t0067g0010 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.883-7912G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825880 | |||||||
chr12:116825926 | G | A | 2 | a0001c0001t0022g0225 a0001c0002t0001g0065 |
2 | HG02258.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.883-7866G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825926 | |||||||
chr12:116825937 | A | G | 4 | a0001c0001t0003g0085 a0001c0001t0003g0191 a0001c0001t0003g0212 others(1): Show |
4 | HG02040.hp2 NA18954.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-7855A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825937 | |||||||
chr12:116825941 | G | A | 10 | a0001c0001t0005g0104 a0001c0002t0005g0062 a0001c0003t0005g0037 others(7): Show |
10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-7851G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116825941 | |||||||
chr12:116826001 | CTCTG | C | 3 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.883-7785_883-7782d others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116826001 | ||||||
chr12:116826059 | C | T | 8 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-7733C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826059 | |||||||
chr12:116826126 | A | C | 1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-7666A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826126 | |||||||
chr12:116826132 | C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-7660C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826132 | |||||||
chr12:116826252 | C | T | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-7540C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826252 | |||||||
chr12:116826282 | G | A | 9 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(6): Show |
9 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-7510G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826282 | |||||||
chr12:116826291 | A | G | 1 | a0003c0017t0006g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.883-7501A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826291 | |||||||
chr12:116826299 | C | G | 3 | a0001c0009t0010g0049 a0001c0009t0037g0043 a0001c0014t0018g0019 |
3 | HG01106.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.883-7493C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826299 | |||||||
chr12:116826371 | G | A | 1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.883-7421G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826371 | |||||||
chr12:116826377 | C | T | 11 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-7415C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826377 | |||||||
chr12:116826514 | C | G | 1 | a0001c0001t0004g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.883-7278C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826514 | |||||||
chr12:116826551 | A | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0232 |
2 | NA18941.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.883-7241A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826551 | |||||||
chr12:116826619 | C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-7173C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826619 | |||||||
chr12:116826804 | A | G | 6 | a0001c0001t0006g0115 a0001c0001t0009g0116 a0001c0001t0009g0118 others(3): Show |
6 | HG01109.hp2 HG01258.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-6988A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826804 | |||||||
chr12:116826810 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.883-6982T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826810 | |||||||
chr12:116826825 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883-6967A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826825 | |||||||
chr12:116826987 | G | A | 2 | a0001c0003t0016g0035 a0001c0009t0052g0016 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.883-6805G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116826987 | |||||||
chr12:116827219 | C | CA | 16 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(13): Show |
16 | HG00438.hp1 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-6558dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827219 | ||||||
chr12:116827219 | C | CAA | 47 | a0001c0001t0001g0171 a0001c0001t0002g0032 a0001c0001t0004g0095 others(44): Show |
47 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.883-6559_883-6558d others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827219 | ||||||
chr12:116827228 | A | G | 4 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-6564A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827228 | |||||||
chr12:116827231 | A | AGAAAGAA others(141): Show |
1 | a0001c0011t0040g0012 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(150): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | |||||||
chr12:116827231 | A | AGAAAGAA others(131): Show |
1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(140): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | |||||||
chr12:116827231 | A | AGAAAGAA others(137): Show |
1 | a0001c0009t0023g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883-6561_883-6560i others(146): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | |||||||
chr12:116827231 | A | AGAAAGAA others(137): Show |
1 | a0001c0011t0023g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.883-6561_883-6560i others(146): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | |||||||
chr12:116827231 | A | G | 2 | a0001c0001t0001g0069 a0001c0002t0001g0251 |
2 | HG02080.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.883-6561A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827231 | |||||||
chr12:116827334 | C | T | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.883-6458C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827334 | |||||||
chr12:116827503 | TC | T | 6 | a0001c0009t0010g0049 a0001c0009t0037g0043 a0001c0009t0052g0016 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-6285delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116827503 | ||||||
chr12:116827698 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-6094C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116827698 | |||||||
chr12:116828010 | C | T | 9 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(6): Show |
9 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-5782C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828010 | |||||||
chr12:116828011 | A | G | 26 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(23): Show |
26 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.883-5781A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828011 | |||||||
chr12:116828131 | C | T | 11 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-5661C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828131 | |||||||
chr12:116828157 | T | G | 3 | a0001c0005t0013g0186 a0001c0013t0013g0159 a0001c0018t0056g0058 |
3 | HG03453.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.883-5635T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828157 | |||||||
chr12:116828353 | G | A | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-5439G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828353 | |||||||
chr12:116828506 | A | G | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-5286A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828506 | |||||||
chr12:116828932 | G | A | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.883-4860G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116828932 | |||||||
chr12:116829005 | G | GA | 8 | a0001c0001t0002g0178 a0001c0001t0070g0068 a0001c0002t0005g0003 others(5): Show |
8 | HG01109.hp1 HG01175.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-4775dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116829005 | ||||||
chr12:116829175 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0223 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.883-4617A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829175 | |||||||
chr12:116829252 | T | G | 1 | a0001c0001t0017g0175 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.883-4540T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829252 | |||||||
chr12:116829376 | C | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4416C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829376 | |||||||
chr12:116829502 | G | C | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4290G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829502 | |||||||
chr12:116829608 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-4184A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829608 | |||||||
chr12:116829617 | G | C | 1 | a0001c0004t0002g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.883-4175G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829617 | |||||||
chr12:116829632 | C | G | 5 | a0001c0001t0007g0070 a0001c0001t0007g0071 a0001c0001t0007g0087 others(2): Show |
5 | HG00544.hp1 HG02523.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-4160C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829632 | |||||||
chr12:116829741 | G | A | 5 | a0001c0009t0010g0049 a0001c0009t0037g0043 a0001c0009t0052g0016 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-4051G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829741 | |||||||
chr12:116829849 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-3943G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829849 | |||||||
chr12:116829893 | T | C | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-3899T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829893 | |||||||
chr12:116829913 | C | T | 4 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-3879C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116829913 | |||||||
chr12:116829962 | A | AT | 6 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0001c0006t0036g0018 others(3): Show |
6 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-3818dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116829962 | ||||||
chr12:116830046 | G | T | 9 | a0001c0009t0010g0049 a0001c0009t0023g0028 a0001c0009t0037g0043 others(6): Show |
9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.883-3746G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830046 | |||||||
chr12:116830524 | G | A | 1 | a0001c0003t0006g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.883-3268G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830524 | |||||||
chr12:116830683 | G | C | 10 | a0001c0001t0005g0104 a0001c0002t0005g0062 a0001c0003t0005g0037 others(7): Show |
10 | HG01243.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-3109G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830683 | |||||||
chr12:116830853 | G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-2939G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830853 | |||||||
chr12:116830902 | C | T | 1 | a0001c0008t0028g0214 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.883-2890C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116830902 | |||||||
chr12:116830907 | C | CA | 7 | a0001c0001t0010g0226 a0001c0001t0019g0124 a0001c0001t0019g0153 others(4): Show |
7 | HG00140.hp1 HG00423.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-2872dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116830907 | ||||||
chr12:116831078 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2714G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831078 | |||||||
chr12:116831095 | C | G | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-2697C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831095 | |||||||
chr12:116831198 | C | CA | 182 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(179): Show |
182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.883-2582dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831198 | ||||||
chr12:116831426 | C | T | 1 | a0001c0002t0012g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.883-2366C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831426 | |||||||
chr12:116831534 | C | CT | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2246dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831534 | ||||||
chr12:116831574 | A | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-2218A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831574 | |||||||
chr12:116831644 | TTAGAG | T | 5 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0002c0010t0002g0001 others(2): Show |
5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-2145_883-2141d others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116831644 | ||||||
chr12:116831784 | GC | G | 16 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(13): Show |
16 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-2007delC | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831784 | |||||||
chr12:116831819 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883-1973C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831819 | |||||||
chr12:116831879 | A | G | 10 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0002t0005g0003 others(7): Show |
10 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-1913A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116831879 | |||||||
chr12:116832130 | CAAAAAA | C | 7 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-1648_883-1643d others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832130 | ||||||
chr12:116832140 | A | ATATATAT others(10): Show |
1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.883-1652_883-1651i others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832140 | |||||||
chr12:116832140 | A | ATATATAT others(18): Show |
1 | a0001c0013t0020g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-1652_883-1651i others(27): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832140 | |||||||
chr12:116832142 | A | AATATATA others(15): Show |
1 | a0001c0002t0018g0022 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-1649_883-1648i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832142 | ||||||
chr12:116832142 | A | T | 3 | a0001c0003t0014g0063 a0001c0005t0020g0161 a0001c0013t0020g0098 |
3 | HG02970.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.883-1650A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832142 | |||||||
chr12:116832144 | A | AAT | 7 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(4): Show |
7 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1647_883-1646i others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | ||||||
chr12:116832144 | A | AATAT | 11 | a0001c0001t0001g0094 a0001c0001t0001g0205 a0001c0001t0002g0031 others(8): Show |
11 | HG00673.hp2 HG02071.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.883-1647_883-1646i others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | ||||||
chr12:116832144 | A | AATATATA others(11): Show |
1 | a0001c0001t0002g0210 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.883-1647_883-1646i others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832144 | ||||||
chr12:116832144 | A | AT | 5 | a0001c0001t0011g0099 a0001c0001t0011g0157 a0001c0001t0049g0184 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1648_883-1647i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | |||||||
chr12:116832144 | A | ATAT | 5 | a0001c0001t0001g0196 a0001c0001t0002g0023 a0001c0001t0061g0090 others(2): Show |
5 | HG00609.hp1 HG00741.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-1648_883-1647i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | |||||||
chr12:116832144 | A | ATATAT | 3 | a0001c0001t0001g0216 a0001c0001t0001g0243 a0001c0001t0015g0112 |
3 | HG00673.hp1 HG02273.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.883-1648_883-1647i others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | |||||||
chr12:116832144 | A | T | 10 | a0001c0002t0002g0110 a0001c0002t0011g0097 a0001c0002t0018g0022 others(7): Show |
10 | HG01169.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-1648A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832144 | |||||||
chr12:116832146 | A | AAT | 6 | a0001c0001t0001g0262 a0001c0001t0009g0118 a0001c0001t0009g0156 others(3): Show |
6 | HG01257.hp1 HG02683.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1645_883-1644i others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | ||||||
chr12:116832146 | A | AATATATA others(5): Show |
1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-1645_883-1644i others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | ||||||
chr12:116832146 | A | AATATATA others(17): Show |
1 | a0002c0010t0002g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883-1645_883-1644i others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | ||||||
chr12:116832146 | A | AATATATA others(23): Show |
1 | a0001c0003t0016g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.883-1645_883-1644i others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832146 | ||||||
chr12:116832146 | A | AT | 20 | a0001c0001t0002g0032 a0001c0001t0004g0167 a0001c0001t0004g0172 others(17): Show |
20 | HG01074.hp2 HG01175.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | |||||||
chr12:116832146 | A | ATAT | 39 | a0001c0001t0001g0069 a0001c0001t0001g0119 a0001c0001t0001g0122 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | |||||||
chr12:116832146 | A | ATATAT | 23 | a0001c0001t0001g0072 a0001c0001t0001g0164 a0001c0001t0001g0198 others(20): Show |
23 | HG00621.hp1 HG01361.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-1646_883-1645i others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | |||||||
chr12:116832146 | A | ATATATAT others(8): Show |
1 | a0001c0002t0065g0093 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.883-1646_883-1645i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | |||||||
chr12:116832146 | A | T | 51 | a0001c0001t0001g0094 a0001c0001t0001g0196 a0001c0001t0001g0205 others(48): Show |
51 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.883-1646A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832146 | |||||||
chr12:116832148 | A | AAAAAATA others(15): Show |
1 | a0002c0010t0002g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.883-1643_883-1642i others(24): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | ||||||
chr12:116832148 | A | AAAAATAT others(8): Show |
3 | a0001c0002t0064g0263 a0001c0007t0005g0060 a0001c0007t0016g0059 |
3 | HG01243.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.883-1643_883-1642i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | ||||||
chr12:116832148 | A | AAATATAT others(8): Show |
2 | a0001c0006t0005g0017 a0001c0007t0034g0061 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.883-1643_883-1642i others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832148 | ||||||
chr12:116832148 | A | AT | 10 | a0001c0001t0004g0109 a0001c0001t0004g0166 a0001c0001t0004g0183 others(7): Show |
10 | HG03130.hp2 HG03209.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-1644_883-1643i others(3): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | ATAT | 25 | a0001c0001t0001g0086 a0001c0001t0001g0168 a0001c0001t0001g0171 others(22): Show |
25 | HG01099.hp1 HG01109.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.883-1644_883-1643i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | ATATATAT others(16): Show |
1 | a0001c0004t0001g0083 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.883-1644_883-1643i others(25): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | ATATATAT others(20): Show |
1 | a0001c0003t0021g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883-1644_883-1643i others(29): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | ATATATAT others(22): Show |
2 | a0001c0001t0005g0104 a0001c0003t0005g0037 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.883-1644_883-1643i others(31): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | ATATATAT others(26): Show |
1 | a0001c0003t0005g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883-1644_883-1643i others(35): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832148 | A | T | 186 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0092 others(183): Show |
186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.883-1644A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832148 | |||||||
chr12:116832150 | T | A | 2 | a0001c0009t0023g0028 a0001c0011t0023g0007 |
2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.883-1642T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832150 | |||||||
chr12:116832239 | C | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.883-1553C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832239 | |||||||
chr12:116832458 | G | A | 3 | a0001c0009t0010g0049 a0001c0009t0037g0043 a0001c0014t0018g0019 |
3 | HG01106.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.883-1334G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832458 | |||||||
chr12:116832631 | C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-1161C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832631 | |||||||
chr12:116832867 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.883-925C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116832867 | |||||||
chr12:116832898 | C | CT | 188 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0001g0092 others(185): Show |
188 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.883-870dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832898 | ||||||
chr12:116832898 | C | CTT | 26 | a0001c0001t0001g0072 a0001c0001t0001g0094 a0001c0001t0001g0144 others(23): Show |
26 | HG00140.hp1 HG00438.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.883-871_883-870dup others(2): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 116832898 | ||||||
chr12:116833002 | C | T | 49 | a0001c0001t0001g0141 a0001c0001t0001g0190 a0001c0001t0001g0193 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.883-790C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833002 | |||||||
chr12:116833042 | C | T | 53 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(50): Show |
53 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.883-750C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833042 | |||||||
chr12:116833101 | T | C | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.883-691T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833101 | |||||||
chr12:116833296 | G | A | 1 | a0001c0004t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-496G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833296 | |||||||
chr12:116833387 | C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-405C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833387 | |||||||
chr12:116833442 | C | T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.883-350C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833442 | |||||||
chr12:116833498 | T | C | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883-294T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833498 | |||||||
chr12:116833630 | A | G | 1 | a0001c0001t0007g0231 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.883-162A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833630 | |||||||
chr12:116833720 | C | T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883-72C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 7/10 | chr12 | 116833720 | |||||||
chr12:116834187 | C | T | 4 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032+246C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834187 | |||||||
chr12:116834242 | A | G | 62 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(59): Show |
62 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1032+301A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834242 | |||||||
chr12:116834270 | A | G | 9 | a0001c0009t0010g0049 a0001c0009t0023g0028 a0001c0009t0037g0043 others(6): Show |
9 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1032+329A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834270 | |||||||
chr12:116834410 | C | T | 5 | a0001c0009t0010g0049 a0001c0009t0037g0043 a0001c0009t0052g0016 others(2): Show |
5 | HG01106.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+469C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834410 | |||||||
chr12:116834441 | A | G | 1 | a0001c0003t0043g0222 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1032+500A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834441 | |||||||
chr12:116834625 | A | C | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1032+684A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834625 | |||||||
chr12:116834678 | G | A | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1032+737G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116834678 | |||||||
chr12:116834850 | C | CT | 8 | a0001c0001t0046g0114 a0001c0002t0001g0075 a0001c0006t0051g0013 others(5): Show |
8 | HG00741.hp1 HG01106.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1032+927dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116834850 | ||||||
chr12:116834850 | CT | C | 42 | a0001c0001t0001g0171 a0001c0001t0002g0032 a0001c0001t0004g0095 others(39): Show |
42 | HG00544.hp1 HG01243.hp1 HG02074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1032+927delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116834850 | ||||||
chr12:116835041 | T | C | 2 | a0001c0002t0002g0129 a0001c0015t0002g0020 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1033-919T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835041 | |||||||
chr12:116835300 | T | TCTC | 171 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(168): Show |
171 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1033-658_1033-657i others(5): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 116835300 | ||||||
chr12:116835567 | T | C | 1 | a0001c0005t0013g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1033-393T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835567 | |||||||
chr12:116835763 | G | A | 1 | a0001c0001t0004g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1033-197G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 8/10 | chr12 | 116835763 | |||||||
chr12:116836050 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1098+25A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836050 | |||||||
chr12:116836058 | C | T | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1098+33C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836058 | |||||||
chr12:116836130 | G | A | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1099-51G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 9/10 | chr12 | 116836130 | |||||||
chr12:116836299 | C | A | 1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1200+17C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836299 | |||||||
chr12:116836358 | G | A | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+76G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836358 | |||||||
chr12:116836430 | A | G | 1 | a0001c0002t0005g0003 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1200+148A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836430 | |||||||
chr12:116836489 | G | C | 1 | a0001c0001t0041g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1200+207G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836489 | |||||||
chr12:116836523 | G | A | 6 | a0001c0005t0013g0006 a0001c0005t0013g0186 a0001c0005t0055g0021 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+241G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836523 | |||||||
chr12:116836606 | C | T | 2 | a0001c0001t0019g0187 a0001c0001t0058g0188 |
2 | HG01261.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1200+324C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836606 | |||||||
chr12:116836640 | A | G | 2 | a0001c0001t0005g0104 a0001c0003t0021g0040 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1200+358A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836640 | |||||||
chr12:116836763 | A | G | 9 | a0001c0005t0013g0006 a0001c0005t0013g0186 a0001c0005t0030g0051 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+481A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836763 | |||||||
chr12:116836841 | A | T | 2 | a0001c0002t0004g0005 a0001c0002t0050g0004 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1200+559A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836841 | |||||||
chr12:116836938 | A | C | 1 | a0001c0002t0002g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1200+656A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116836938 | |||||||
chr12:116837268 | C | T | 2 | a0001c0009t0052g0016 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1200+986C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837268 | |||||||
chr12:116837369 | T | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0189 |
2 | HG00408.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.1200+1087T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837369 | |||||||
chr12:116837388 | G | T | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+1106G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837388 | |||||||
chr12:116837572 | T | C | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+1290T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837572 | |||||||
chr12:116837628 | A | G | 1 | a0001c0006t0051g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1200+1346A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837628 | |||||||
chr12:116837773 | A | G | 1 | a0001c0001t0011g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1200+1491A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837773 | |||||||
chr12:116837797 | A | G | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+1515A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837797 | |||||||
chr12:116837932 | A | G | 1 | a0001c0001t0010g0226 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1200+1650A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837932 | |||||||
chr12:116837958 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1200+1676G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116837958 | |||||||
chr12:116838022 | T | TA | 41 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(38): Show |
41 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1200+1749dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116838022 | ||||||
chr12:116838046 | C | T | 36 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(33): Show |
36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+1764C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838046 | |||||||
chr12:116838106 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+1824T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838106 | |||||||
chr12:116838211 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1200+1929G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838211 | |||||||
chr12:116838412 | T | C | 257 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(254): Show |
257 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.1200+2130T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838412 | |||||||
chr12:116838420 | A | C | 62 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(59): Show |
62 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1200+2138A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838420 | |||||||
chr12:116838461 | T | C | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1200+2179T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838461 | |||||||
chr12:116838498 | G | C | 11 | a0001c0001t0002g0210 a0001c0002t0018g0022 a0001c0004t0001g0083 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+2216G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838498 | |||||||
chr12:116838581 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1200+2299A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838581 | |||||||
chr12:116838706 | A | G | 59 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(56): Show |
59 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1200+2424A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116838706 | |||||||
chr12:116839045 | G | A | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+2763G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839045 | |||||||
chr12:116839105 | G | A | 7 | a0001c0003t0035g0088 a0001c0009t0010g0049 a0001c0009t0037g0043 others(4): Show |
7 | HG01106.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2823G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839105 | |||||||
chr12:116839293 | T | TTGGA | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+3028_1200+303 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839293 | ||||||
chr12:116839336 | G | A | 2 | a0001c0001t0070g0068 a0001c0002t0010g0132 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1200+3054G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839336 | |||||||
chr12:116839352 | G | A | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+3070G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839352 | |||||||
chr12:116839392 | A | G | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+3110A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839392 | |||||||
chr12:116839413 | ATGGG | A | 11 | a0001c0001t0002g0210 a0001c0002t0005g0163 a0001c0002t0018g0022 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+3143_1200+314 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839413 | ||||||
chr12:116839417 | G | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+3135G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839417 | |||||||
chr12:116839421 | G | GTGGATGG others(5): Show |
1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+3142_1200+314 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | ||||||
chr12:116839421 | GTGGGTGG others(1): Show |
G | 14 | a0001c0001t0005g0245 a0001c0001t0005g0246 a0001c0001t0019g0124 others(11): Show |
14 | HG00140.hp1 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.1200+3143_1200+315 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | ||||||
chr12:116839421 | GTGGGTGG others(5): Show |
G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+3143_1200+315 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839421 | ||||||
chr12:116839425 | G | A | 7 | a0001c0003t0035g0088 a0001c0004t0001g0091 a0001c0009t0010g0049 others(4): Show |
7 | HG00621.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+3143G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839425 | |||||||
chr12:116839425 | GTGGA | G | 169 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(166): Show |
169 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1200+3178_1200+318 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839425 | ||||||
chr12:116839425 | GTGGATGG others(1): Show |
G | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+3174_1200+318 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839425 | ||||||
chr12:116839429 | A | G | 1 | a0001c0001t0017g0213 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1200+3147A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839429 | |||||||
chr12:116839486 | G | C | 5 | a0001c0001t0002g0210 a0001c0004t0001g0083 a0002c0010t0002g0001 others(2): Show |
5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+3204G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839486 | |||||||
chr12:116839774 | A | AAGGG | 7 | a0001c0001t0026g0182 a0001c0005t0013g0006 a0001c0005t0013g0186 others(4): Show |
7 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+3509_1200+351 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116839774 | ||||||
chr12:116839859 | A | G | 1 | a0001c0002t0003g0008 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1200+3577A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839859 | |||||||
chr12:116839912 | G | A | 5 | a0001c0001t0002g0036 a0001c0001t0002g0103 a0001c0001t0002g0105 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+3630G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116839912 | |||||||
chr12:116840148 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1200+3866C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840148 | |||||||
chr12:116840317 | A | C | 10 | a0001c0003t0035g0088 a0001c0009t0010g0049 a0001c0009t0023g0028 others(7): Show |
10 | HG01106.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+4035A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840317 | |||||||
chr12:116840328 | A | G | 3 | a0001c0003t0002g0100 a0001c0003t0002g0101 a0001c0003t0002g0102 |
3 | HG01074.hp2 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1200+4046A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840328 | |||||||
chr12:116840399 | C | G | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+4117C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840399 | |||||||
chr12:116840590 | G | A | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+4308G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840590 | |||||||
chr12:116840607 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1200+4325C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840607 | |||||||
chr12:116840616 | A | G | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+4334A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840616 | |||||||
chr12:116840829 | T | C | 6 | a0001c0001t0005g0104 a0001c0002t0005g0062 a0001c0003t0005g0037 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+4547T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116840829 | |||||||
chr12:116840922 | C | CTG | 178 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(175): Show |
178 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.1200+4660_1200+466 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116840922 | ||||||
chr12:116841063 | A | T | 245 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(242): Show |
245 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.1200+4781A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841063 | |||||||
chr12:116841214 | G | A | 1 | a0001c0003t0006g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1200+4932G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841214 | |||||||
chr12:116841465 | T | C | 52 | a0001c0001t0001g0171 a0001c0001t0002g0210 a0001c0001t0004g0095 others(49): Show |
52 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1200+5183T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841465 | |||||||
chr12:116841522 | C | T | 36 | a0001c0001t0001g0171 a0001c0001t0004g0095 a0001c0001t0004g0096 others(33): Show |
36 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+5240C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841522 | |||||||
chr12:116841523 | G | A | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1200+5241G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841523 | |||||||
chr12:116841558 | G | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5276G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841558 | |||||||
chr12:116841606 | G | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5324G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841606 | |||||||
chr12:116841623 | C | A | 15 | a0001c0001t0002g0210 a0001c0001t0019g0124 a0001c0001t0019g0153 others(12): Show |
15 | HG00140.hp1 HG00438.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1200+5341C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841623 | |||||||
chr12:116841760 | AATATAAA others(33): Show |
A | 4 | a0001c0001t0002g0210 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5496_1200+553 others(44): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841760 | ||||||
chr12:116841766 | AAT | A | 4 | a0001c0004t0053g0015 a0001c0007t0025g0009 a0001c0007t0025g0057 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5496_1200+549 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841766 | ||||||
chr12:116841776 | TATAAATA others(111): Show |
T | 2 | a0001c0001t0005g0104 a0001c0003t0021g0040 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1200+5498_1200+561 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841776 | ||||||
chr12:116841778 | T | A | 2 | a0001c0005t0020g0161 a0001c0013t0020g0098 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+5496T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841778 | |||||||
chr12:116841780 | A | T | 1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5498A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841780 | |||||||
chr12:116841782 | TATATATA others(81): Show |
T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+5522_1200+560 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841782 | ||||||
chr12:116841784 | TATATATA others(3): Show |
T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5512_1200+552 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841784 | ||||||
chr12:116841784 | TATATATA others(103): Show |
T | 1 | a0001c0001t0004g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1200+5512_1200+562 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841784 | ||||||
chr12:116841790 | TATAAATA others(97): Show |
T | 8 | a0001c0002t0005g0062 a0001c0003t0005g0037 a0001c0003t0005g0038 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5512_1200+561 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841790 | ||||||
chr12:116841792 | T | A | 6 | a0001c0001t0012g0261 a0001c0001t0019g0124 a0001c0001t0019g0153 others(3): Show |
6 | HG00140.hp1 HG01192.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+5510T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841792 | |||||||
chr12:116841792 | TAAATATA others(93): Show |
T | 22 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0143 others(19): Show |
22 | HG00544.hp1 HG01243.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1200+5524_1200+562 others(104): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841792 | ||||||
chr12:116841794 | A | AAT | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5522_1200+552 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841794 | ||||||
chr12:116841794 | A | T | 4 | a0001c0001t0004g0095 a0001c0001t0004g0172 a0001c0001t0004g0183 others(1): Show |
4 | HG01192.hp1 HG02647.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5512A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841794 | |||||||
chr12:116841794 | AATATATA others(95): Show |
A | 9 | a0001c0001t0002g0105 a0001c0004t0053g0015 a0001c0005t0013g0006 others(6): Show |
9 | HG00741.hp1 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5574_1200+567 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841794 | ||||||
chr12:116841796 | TATATATA others(91): Show |
T | 2 | a0001c0001t0004g0172 a0001c0001t0004g0183 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1200+5524_1200+562 others(102): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841796 | ||||||
chr12:116841798 | T | A | 1 | a0001c0001t0004g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1200+5516T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841798 | |||||||
chr12:116841804 | TAAATATA others(45): Show |
T | 1 | a0001c0001t0014g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1200+5538_1200+558 others(56): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841804 | ||||||
chr12:116841804 | TAAATATA others(81): Show |
T | 10 | a0001c0001t0001g0196 a0001c0001t0001g0206 a0001c0001t0001g0230 others(7): Show |
10 | HG00423.hp1 HG00673.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+5536_1200+562 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841804 | ||||||
chr12:116841806 | A | T | 2 | a0001c0002t0018g0047 a0001c0014t0002g0139 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1200+5524A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841806 | |||||||
chr12:116841806 | AATATATA others(83): Show |
A | 2 | a0001c0001t0012g0261 a0001c0001t0022g0225 |
2 | HG01192.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1200+5538_1200+562 others(94): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841806 | ||||||
chr12:116841808 | T | A | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+5526T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841808 | |||||||
chr12:116841808 | TATATATA others(31): Show |
T | 4 | a0001c0001t0011g0099 a0001c0001t0011g0157 a0001c0002t0011g0097 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5550_1200+558 others(42): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841808 | ||||||
chr12:116841808 | TATATATA others(43): Show |
T | 7 | a0001c0001t0001g0069 a0001c0002t0001g0079 a0001c0002t0001g0080 others(4): Show |
7 | HG01099.hp2 HG01358.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+5536_1200+558 others(54): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841808 | ||||||
chr12:116841812 | TATATAAA others(75): Show |
T | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1200+5536_1200+561 others(86): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841812 | ||||||
chr12:116841812 | TATATAAA others(145): Show |
T | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+5532_1200+568 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841812 | ||||||
chr12:116841814 | TATAAAAA others(73): Show |
T | 8 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5536_1200+561 others(84): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841814 | ||||||
chr12:116841816 | TAAAAATA others(33): Show |
T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5538_1200+557 others(44): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841816 | ||||||
chr12:116841818 | A | T | 141 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(138): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1200+5536A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841818 | |||||||
chr12:116841818 | AAAATATA others(71): Show |
A | 10 | a0001c0001t0001g0248 a0001c0001t0005g0245 a0001c0001t0005g0246 others(7): Show |
10 | HG01175.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1200+5538_1200+561 others(82): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841818 | ||||||
chr12:116841819 | A | T | 1 | a0001c0002t0001g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1200+5537A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841819 | |||||||
chr12:116841820 | A | T | 6 | a0001c0002t0005g0149 a0001c0002t0005g0151 a0001c0002t0033g0150 others(3): Show |
6 | HG01106.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+5538A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841820 | |||||||
chr12:116841820 | AATATATA others(69): Show |
A | 121 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0092 others(118): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1200+5550_1200+562 others(80): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841820 | ||||||
chr12:116841820 | AATATATA others(97): Show |
A | 4 | a0001c0002t0065g0093 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5550_1200+565 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841820 | ||||||
chr12:116841822 | T | A | 1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5540T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841822 | |||||||
chr12:116841822 | T | TATATATA others(3): Show |
1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+5549_1200+555 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | ||||||
chr12:116841822 | T | TATATATA others(41): Show |
1 | a0001c0006t0006g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1200+5562_1200+560 others(52): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | ||||||
chr12:116841822 | TATATATA others(5): Show |
T | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1200+5562_1200+557 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841822 | ||||||
chr12:116841828 | TATATAAA others(59): Show |
T | 3 | a0001c0002t0005g0149 a0001c0002t0005g0151 a0001c0002t0033g0150 |
3 | HG02922.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1200+5552_1200+561 others(70): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841828 | ||||||
chr12:116841828 | TATATAAA others(87): Show |
T | 1 | a0001c0002t0001g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1200+5552_1200+564 others(98): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841828 | ||||||
chr12:116841830 | TATAAATA others(57): Show |
T | 1 | a0001c0001t0002g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1200+5552_1200+561 others(68): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841830 | ||||||
chr12:116841832 | T | A | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5550T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841832 | |||||||
chr12:116841832 | TAAATATA others(81): Show |
T | 2 | a0001c0006t0036g0018 a0001c0011t0054g0011 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1200+5564_1200+565 others(92): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841832 | ||||||
chr12:116841834 | A | T | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5552A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841834 | |||||||
chr12:116841836 | TATATATA others(3): Show |
T | 1 | a0001c0001t0019g0124 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1200+5566_1200+557 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841836 | ||||||
chr12:116841836 | TATATATA others(15): Show |
T | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1200+5564_1200+558 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841836 | ||||||
chr12:116841844 | TAAATATA others(5): Show |
T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5574_1200+558 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | ||||||
chr12:116841844 | TAAATATA others(30): Show |
T | 1 | a0001c0003t0014g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5565_1200+560 others(41): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | ||||||
chr12:116841844 | TAAATATA others(111): Show |
T | 3 | a0001c0001t0004g0095 a0001c0002t0002g0129 a0001c0015t0002g0020 |
3 | HG02258.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1200+5564_1200+568 others(4): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841844 | ||||||
chr12:116841846 | A | T | 2 | a0001c0005t0020g0161 a0001c0013t0020g0098 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+5564A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841846 | |||||||
chr12:116841846 | AATATATA others(1): Show |
A | 4 | a0001c0001t0019g0187 a0001c0001t0057g0220 a0001c0001t0058g0188 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5566_1200+557 others(12): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841846 | ||||||
chr12:116841848 | TATATATA others(3): Show |
T | 4 | a0001c0001t0002g0210 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5574_1200+558 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841848 | ||||||
chr12:116841848 | TATATATA others(27): Show |
T | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5574_1200+560 others(38): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841848 | ||||||
chr12:116841850 | TATATAAA others(25): Show |
T | 9 | a0001c0001t0014g0039 a0001c0001t0070g0068 a0001c0002t0002g0110 others(6): Show |
9 | HG01074.hp2 HG01109.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5574_1200+560 others(36): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841850 | ||||||
chr12:116841856 | A | T | 7 | a0001c0001t0011g0099 a0001c0001t0011g0157 a0001c0002t0011g0097 others(4): Show |
7 | HG02451.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+5574A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841856 | |||||||
chr12:116841858 | A | T | 7 | a0001c0001t0019g0153 a0001c0001t0019g0187 a0001c0001t0057g0220 others(4): Show |
7 | HG00140.hp1 HG01261.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+5576A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841858 | |||||||
chr12:116841860 | T | A | 1 | a0001c0003t0006g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1200+5578T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841860 | |||||||
chr12:116841868 | T | A | 2 | a0001c0001t0019g0153 a0001c0009t0010g0049 |
2 | HG02735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1200+5586T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841868 | |||||||
chr12:116841870 | A | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1200+5588A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841870 | |||||||
chr12:116841871 | A | T | 1 | a0001c0006t0031g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1200+5589A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841871 | |||||||
chr12:116841882 | A | AAT | 4 | a0001c0001t0002g0210 a0001c0006t0031g0067 a0002c0010t0002g0001 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5608_1200+560 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | ||||||
chr12:116841882 | A | AATATATA others(59): Show |
1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+5621_1200+562 others(70): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | ||||||
chr12:116841882 | A | AATATATA others(21): Show |
1 | a0003c0017t0006g0056 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1200+5640_1200+566 others(32): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | ||||||
chr12:116841882 | A | AATATATA others(83): Show |
1 | a0001c0009t0037g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1200+5609_1200+561 others(94): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841882 | ||||||
chr12:116841882 | A | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5600A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841882 | |||||||
chr12:116841883 | A | T | 1 | a0001c0016t0032g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1200+5601A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841883 | |||||||
chr12:116841884 | T | A | 4 | a0001c0001t0019g0124 a0001c0001t0019g0187 a0001c0001t0057g0220 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5602T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841884 | |||||||
chr12:116841892 | A | T | 31 | a0001c0001t0001g0069 a0001c0001t0002g0210 a0001c0001t0011g0099 others(28): Show |
31 | HG00140.hp1 HG00438.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1200+5610A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841892 | |||||||
chr12:116841892 | AAAAT | A | 9 | a0001c0001t0014g0039 a0001c0001t0070g0068 a0001c0002t0002g0110 others(6): Show |
9 | HG01074.hp2 HG01109.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+5612_1200+561 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841892 | ||||||
chr12:116841894 | A | T | 45 | a0001c0001t0001g0069 a0001c0001t0001g0171 a0001c0001t0001g0196 others(42): Show |
45 | HG00140.hp1 HG00544.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.1200+5612A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841894 | |||||||
chr12:116841894 | AAT | A | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+5624_1200+562 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841894 | ||||||
chr12:116841896 | T | A | 28 | a0001c0001t0001g0069 a0001c0001t0001g0196 a0001c0001t0001g0206 others(25): Show |
28 | HG00140.hp1 HG00741.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1200+5614T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841896 | |||||||
chr12:116841896 | T | TATATATA others(15): Show |
1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+5621_1200+562 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841896 | ||||||
chr12:116841900 | T | A | 34 | a0001c0001t0001g0171 a0001c0001t0004g0109 a0001c0001t0004g0143 others(31): Show |
34 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1200+5618T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841900 | |||||||
chr12:116841902 | T | A | 8 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+5620T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841902 | |||||||
chr12:116841904 | T | A | 1 | a0001c0001t0046g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1200+5622T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841904 | |||||||
chr12:116841908 | A | T | 9 | a0001c0001t0002g0032 a0001c0001t0008g0026 a0001c0001t0008g0029 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5626A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841908 | |||||||
chr12:116841920 | A | T | 32 | a0001c0001t0001g0260 a0001c0001t0002g0032 a0001c0001t0002g0210 others(29): Show |
32 | HG00140.hp1 HG00438.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1200+5638A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841920 | |||||||
chr12:116841922 | A | T | 2 | a0001c0001t0019g0153 a0001c0003t0035g0088 |
2 | HG02735.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1200+5640A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841922 | |||||||
chr12:116841924 | TATATATA others(5): Show |
T | 1 | a0001c0003t0006g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1200+5666_1200+567 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841924 | ||||||
chr12:116841934 | T | A | 1 | a0001c0001t0019g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1200+5652T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841934 | |||||||
chr12:116841936 | A | T | 2 | a0001c0001t0019g0153 a0001c0002t0001g0074 |
2 | HG02735.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1200+5654A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841936 | |||||||
chr12:116841938 | T | C | 4 | a0001c0001t0019g0124 a0001c0001t0019g0187 a0001c0001t0057g0220 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5656T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841938 | |||||||
chr12:116841944 | TATAAATA others(9): Show |
T | 1 | a0001c0002t0050g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1200+5664_1200+567 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841944 | ||||||
chr12:116841946 | TAAATATA others(9): Show |
T | 46 | a0001c0001t0001g0171 a0001c0001t0001g0230 a0001c0001t0002g0031 others(43): Show |
46 | HG00423.hp1 HG00544.hp1 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1200+5666_1200+568 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841946 | ||||||
chr12:116841946 | TAAATATA others(15): Show |
T | 2 | a0001c0006t0031g0067 a0001c0016t0032g0044 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1200+5666_1200+568 others(26): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841946 | ||||||
chr12:116841948 | A | T | 5 | a0001c0001t0002g0210 a0001c0013t0020g0098 a0002c0010t0002g0001 others(2): Show |
5 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5666A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841948 | |||||||
chr12:116841950 | T | A | 8 | a0001c0003t0002g0102 a0001c0005t0013g0006 a0001c0005t0013g0186 others(5): Show |
8 | HG01891.hp2 HG02132.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+5668T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841950 | |||||||
chr12:116841952 | T | A | 1 | a0001c0001t0019g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1200+5670T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841952 | |||||||
chr12:116841952 | T | TATATATA others(3): Show |
1 | a0001c0005t0020g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1200+5677_1200+567 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841952 | ||||||
chr12:116841952 | TATATATA others(9): Show |
T | 1 | a0001c0013t0020g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1200+5672_1200+568 others(20): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841952 | ||||||
chr12:116841953 | A | G | 4 | a0001c0002t0065g0093 a0001c0009t0023g0028 a0001c0011t0023g0007 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+5671A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841953 | |||||||
chr12:116841956 | T | G | 1 | a0001c0003t0035g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200+5674T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841956 | |||||||
chr12:116841956 | TATAGAGA others(3): Show |
T | 1 | a0001c0009t0010g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+5676_1200+568 others(14): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841956 | ||||||
chr12:116841956 | TATAGAGA others(7): Show |
T | 3 | a0001c0001t0002g0210 a0002c0010t0002g0001 a0002c0010t0002g0254 |
3 | HG00438.hp1 HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1200+5676_1200+568 others(18): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841956 | ||||||
chr12:116841958 | T | G | 5 | a0001c0003t0035g0088 a0001c0003t0043g0222 a0001c0006t0006g0066 others(2): Show |
5 | HG02818.hp2 HG03654.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5676T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841958 | |||||||
chr12:116841958 | TAGAG | T | 189 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(186): Show |
189 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1200+5701_1200+570 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116841958 | ||||||
chr12:116841960 | G | T | 9 | a0001c0001t0019g0153 a0001c0002t0042g0077 a0001c0003t0006g0054 others(6): Show |
9 | HG00140.hp2 HG01106.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5678G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841960 | |||||||
chr12:116841962 | G | T | 4 | a0001c0001t0019g0153 a0001c0005t0020g0161 a0001c0014t0018g0019 others(1): Show |
4 | HG01106.hp1 HG02132.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+5680G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841962 | |||||||
chr12:116841963 | A | C | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1200+5681A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841963 | |||||||
chr12:116841964 | G | T | 9 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(6): Show |
9 | HG00140.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5682G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841964 | |||||||
chr12:116841966 | G | T | 9 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(6): Show |
9 | HG00140.hp1 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5684G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841966 | |||||||
chr12:116841968 | G | A | 235 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(232): Show |
235 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1200+5686G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841968 | |||||||
chr12:116841968 | G | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG01261.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+5686G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841968 | |||||||
chr12:116841970 | G | T | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG01261.hp2 HG02055.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+5688G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841970 | |||||||
chr12:116841981 | A | G | 1 | a0001c0014t0002g0139 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1200+5699A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116841981 | |||||||
chr12:116842082 | C | T | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1200+5800C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842082 | |||||||
chr12:116842251 | C | T | 44 | a0001c0001t0002g0032 a0001c0001t0002g0133 a0001c0001t0002g0178 others(41): Show |
44 | HG00408.hp2 HG00609.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1200+5969C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842251 | |||||||
chr12:116842322 | G | T | 4 | a0001c0001t0002g0036 a0001c0001t0002g0105 a0001c0001t0002g0253 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+6040G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842322 | |||||||
chr12:116842384 | C | G | 1 | a0001c0001t0008g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1200+6102C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842384 | |||||||
chr12:116842453 | C | G | 1 | a0001c0014t0018g0019 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1200+6171C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842453 | |||||||
chr12:116842568 | ATTTG | A | 89 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0045 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1200+6307_1200+631 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116842568 | ||||||
chr12:116842623 | G | A | 1 | a0001c0002t0068g0042 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1200+6341G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842623 | |||||||
chr12:116842698 | C | A | 3 | a0001c0005t0020g0161 a0001c0013t0020g0098 a0001c0016t0032g0044 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1200+6416C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842698 | |||||||
chr12:116842770 | C | T | 3 | a0001c0005t0030g0051 a0001c0005t0030g0052 a0001c0005t0071g0050 |
3 | HG01891.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1200+6488C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842770 | |||||||
chr12:116842899 | G | A | 1 | a0001c0001t0017g0200 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1201-6415G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842899 | |||||||
chr12:116842983 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1201-6331T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116842983 | |||||||
chr12:116843021 | A | C | 6 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(3): Show |
6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-6293A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843021 | |||||||
chr12:116843160 | A | C | 4 | a0001c0001t0002g0210 a0002c0010t0002g0001 a0002c0010t0002g0002 others(1): Show |
4 | HG00438.hp1 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-6154A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843160 | |||||||
chr12:116843269 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0244 |
2 | HG00408.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1201-6045G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843269 | |||||||
chr12:116843492 | C | CA | 158 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(155): Show |
158 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1201-5799dupA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | ||||||
chr12:116843492 | C | CAA | 39 | a0001c0001t0001g0092 a0001c0001t0001g0141 a0001c0001t0001g0193 others(36): Show |
39 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1201-5800_1201-579 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | ||||||
chr12:116843492 | CAAAA | C | 6 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(3): Show |
6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-5802_1201-579 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843492 | ||||||
chr12:116843512 | A | C | 4 | a0001c0001t0019g0153 a0001c0001t0019g0187 a0001c0001t0057g0220 others(1): Show |
4 | HG00140.hp1 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-5802A>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843512 | |||||||
chr12:116843516 | C | A | 25 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0109 others(22): Show |
25 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1201-5798C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843516 | |||||||
chr12:116843555 | C | T | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-5759C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843555 | |||||||
chr12:116843644 | G | A | 1 | a0001c0002t0005g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1201-5670G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843644 | |||||||
chr12:116843705 | TG | T | 256 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(253): Show |
256 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.1201-5605delG | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116843705 | ||||||
chr12:116843758 | C | G | 2 | a0001c0003t0035g0088 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-5556C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116843758 | |||||||
chr12:116844165 | G | A | 6 | a0001c0001t0001g0190 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG01192.hp1 HG01257.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-5149G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844165 | |||||||
chr12:116844724 | G | T | 6 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(3): Show |
6 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4590G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844724 | |||||||
chr12:116844911 | C | T | 3 | a0001c0005t0020g0161 a0001c0013t0020g0098 a0001c0016t0032g0044 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-4403C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844911 | |||||||
chr12:116844913 | T | C | 39 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0109 others(36): Show |
39 | HG00544.hp1 HG00673.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1201-4401T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116844913 | |||||||
chr12:116845013 | T | C | 1 | a0001c0002t0018g0047 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1201-4301T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845013 | |||||||
chr12:116845209 | A | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-4105A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845209 | |||||||
chr12:116845222 | T | G | 3 | a0001c0002t0018g0022 a0001c0002t0018g0047 a0001c0006t0051g0013 |
3 | HG00741.hp1 HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1201-4092T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845222 | |||||||
chr12:116845243 | CA | C | 8 | a0001c0001t0004g0228 a0001c0001t0008g0026 a0001c0001t0008g0029 others(5): Show |
8 | HG01361.hp1 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4055delA | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845243 | ||||||
chr12:116845243 | CAAA | C | 97 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(94): Show |
97 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1201-4057_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845243 | ||||||
chr12:116845254 | A | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-4060A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845254 | |||||||
chr12:116845256 | A | T | 3 | a0001c0001t0007g0169 a0001c0001t0007g0170 a0001c0009t0052g0016 |
3 | HG02976.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1201-4058A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845256 | |||||||
chr12:116845257 | AAAT | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0164 a0001c0001t0001g0216 others(5): Show |
8 | HG01074.hp1 HG01978.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4055_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845257 | ||||||
chr12:116845258 | A | T | 19 | a0001c0001t0001g0144 a0001c0001t0001g0205 a0001c0001t0001g0211 others(16): Show |
19 | HG00408.hp1 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1201-4056A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845258 | |||||||
chr12:116845259 | AT | A | 27 | a0001c0001t0002g0036 a0001c0001t0002g0105 a0001c0001t0002g0253 others(24): Show |
27 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1201-4054delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845259 | |||||||
chr12:116845259 | ATAT | A | 24 | a0001c0001t0001g0237 a0001c0001t0002g0178 a0001c0001t0002g0179 others(21): Show |
24 | HG00438.hp2 HG01175.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1201-4054_1201-405 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845259 | |||||||
chr12:116845260 | T | A | 76 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0032 others(73): Show |
76 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1201-4054T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845260 | |||||||
chr12:116845262 | T | A | 92 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0032 others(89): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1201-4052T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845262 | |||||||
chr12:116845264 | T | A | 90 | a0001c0001t0002g0023 a0001c0001t0002g0036 a0001c0001t0002g0105 others(87): Show |
90 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1201-4050T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845264 | |||||||
chr12:116845266 | T | A | 20 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0189 others(17): Show |
20 | HG00438.hp2 HG01175.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1201-4048T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845266 | |||||||
chr12:116845268 | T | A | 6 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0189 others(3): Show |
6 | HG00438.hp2 HG02071.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-4046T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845268 | |||||||
chr12:116845272 | T | G | 1 | a0001c0002t0004g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1201-4042T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845272 | |||||||
chr12:116845274 | T | G | 9 | a0001c0001t0001g0141 a0001c0001t0001g0235 a0001c0001t0001g0244 others(6): Show |
9 | HG01099.hp2 HG01243.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-4040T>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845274 | |||||||
chr12:116845274 | TAG | T | 12 | a0001c0002t0002g0265 a0001c0002t0010g0266 a0001c0005t0013g0006 others(9): Show |
12 | HG01106.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-4019_1201-401 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | ||||||
chr12:116845274 | TAGAG | T | 87 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0032 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1201-4021_1201-401 others(8): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | ||||||
chr12:116845274 | TAGAGAG | T | 4 | a0001c0002t0068g0042 a0001c0007t0025g0009 a0001c0007t0025g0057 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-4023_1201-401 others(10): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116845274 | ||||||
chr12:116845276 | G | T | 104 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1201-4038G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845276 | |||||||
chr12:116845278 | G | T | 67 | a0001c0001t0001g0092 a0001c0001t0001g0164 a0001c0001t0001g0196 others(64): Show |
67 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1201-4036G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845278 | |||||||
chr12:116845280 | G | T | 123 | a0001c0001t0001g0164 a0001c0001t0001g0230 a0001c0001t0002g0023 others(120): Show |
123 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1201-4034G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845280 | |||||||
chr12:116845282 | G | T | 100 | a0001c0001t0001g0164 a0001c0001t0002g0023 a0001c0001t0002g0031 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1201-4032G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845282 | |||||||
chr12:116845284 | G | T | 37 | a0001c0001t0002g0133 a0001c0001t0002g0178 a0001c0001t0002g0179 others(34): Show |
37 | HG00408.hp2 HG00438.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1201-4030G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845284 | |||||||
chr12:116845337 | T | A | 1 | a0002c0010t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1201-3977T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845337 | |||||||
chr12:116845446 | A | G | 2 | a0001c0003t0035g0088 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3868A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845446 | |||||||
chr12:116845447 | A | G | 2 | a0001c0003t0035g0088 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3867A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845447 | |||||||
chr12:116845450 | T | A | 2 | a0001c0003t0035g0088 a0001c0014t0018g0019 |
2 | HG01106.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1201-3864T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845450 | |||||||
chr12:116845564 | A | G | 1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-3750A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845564 | |||||||
chr12:116845648 | G | A | 19 | a0001c0001t0005g0104 a0001c0001t0005g0245 a0001c0001t0005g0246 others(16): Show |
19 | HG01175.hp2 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1201-3666G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845648 | |||||||
chr12:116845728 | C | T | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-3586C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845728 | |||||||
chr12:116845787 | C | T | 9 | a0001c0005t0013g0006 a0001c0005t0013g0186 a0001c0005t0030g0051 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201-3527C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845787 | |||||||
chr12:116845801 | C | A | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-3513C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845801 | |||||||
chr12:116845910 | G | A | 10 | a0001c0001t0002g0031 a0001c0001t0002g0045 a0001c0001t0002g0048 others(7): Show |
10 | HG01169.hp2 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1201-3404G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116845910 | |||||||
chr12:116846203 | C | T | 2 | a0001c0004t0053g0015 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1201-3111C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846203 | |||||||
chr12:116846248 | CATTATTC others(19): Show |
C | 6 | a0001c0001t0005g0104 a0001c0002t0005g0062 a0001c0003t0005g0037 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-3059_1201-303 others(30): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846248 | ||||||
chr12:116846343 | G | A | 1 | a0001c0001t0002g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1201-2971G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846343 | |||||||
chr12:116846409 | G | A | 6 | a0001c0001t0001g0230 a0001c0002t0001g0073 a0001c0002t0001g0074 others(3): Show |
6 | HG00423.hp1 HG02135.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-2905G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846409 | |||||||
chr12:116846412 | C | T | 3 | a0001c0009t0023g0028 a0001c0011t0023g0007 a0001c0011t0040g0012 |
3 | HG02486.hp1 HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-2902C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846412 | |||||||
chr12:116846418 | A | T | 1 | a0001c0002t0008g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1201-2896A>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846418 | |||||||
chr12:116846437 | A | ATTTTTTT others(4): Show |
55 | a0001c0001t0002g0023 a0001c0001t0002g0032 a0001c0001t0002g0036 others(52): Show |
55 | HG00423.hp2 HG00609.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1201-2875_1201-286 others(15): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | ||||||
chr12:116846437 | A | ATTTTTTT others(5): Show |
127 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0092 others(124): Show |
127 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1201-2876_1201-286 others(16): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | ||||||
chr12:116846437 | A | ATTTTTTT others(6): Show |
32 | a0001c0001t0001g0086 a0001c0001t0001g0144 a0001c0001t0001g0171 others(29): Show |
32 | HG00438.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1201-2865_1201-286 others(17): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | ||||||
chr12:116846437 | A | ATTTTTTT others(8): Show |
1 | a0001c0004t0053g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1201-2865_1201-286 others(19): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846437 | ||||||
chr12:116846490 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1201-2824A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846490 | |||||||
chr12:116846498 | C | G | 3 | a0001c0007t0025g0009 a0001c0007t0025g0057 a0001c0007t0047g0053 |
3 | HG01884.hp2 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1201-2816C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846498 | |||||||
chr12:116846543 | G | A | 1 | a0001c0012t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1201-2771G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846543 | |||||||
chr12:116846566 | A | G | 5 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(2): Show |
5 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-2748A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846566 | |||||||
chr12:116846707 | C | T | 1 | a0001c0006t0036g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1201-2607C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846707 | |||||||
chr12:116846824 | C | T | 2 | a0001c0004t0053g0015 a0001c0011t0054g0011 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1201-2490C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846824 | |||||||
chr12:116846901 | AT | A | 29 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0128 others(26): Show |
29 | HG00544.hp1 HG00673.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1201-2392delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | ||||||
chr12:116846901 | ATT | A | 18 | a0001c0001t0001g0086 a0001c0001t0001g0205 a0001c0001t0001g0206 others(15): Show |
18 | HG00140.hp1 HG00408.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1201-2393_1201-239 others(6): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | ||||||
chr12:116846901 | ATTT | A | 193 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0092 others(190): Show |
193 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.1201-2394_1201-239 others(7): Show |
RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116846901 | ||||||
chr12:116846946 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1201-2368T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846946 | |||||||
chr12:116846970 | G | A | 91 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0032 others(88): Show |
91 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1201-2344G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846970 | |||||||
chr12:116846983 | A | G | 26 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0109 others(23): Show |
26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1201-2331A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116846983 | |||||||
chr12:116847001 | T | C | 1 | a0001c0011t0054g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1201-2313T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847001 | |||||||
chr12:116847019 | C | T | 1 | a0001c0001t0017g0175 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1201-2295C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847019 | |||||||
chr12:116847154 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-2160C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847154 | |||||||
chr12:116847298 | C | T | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-2016C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847298 | |||||||
chr12:116847316 | C | T | 6 | a0001c0005t0013g0006 a0001c0005t0013g0186 a0001c0005t0055g0021 others(3): Show |
6 | HG01891.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-1998C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847316 | |||||||
chr12:116847325 | C | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-1989C>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847325 | |||||||
chr12:116847398 | A | G | 2 | a0001c0005t0030g0051 a0001c0005t0030g0052 |
2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1201-1916A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847398 | |||||||
chr12:116847474 | C | G | 96 | a0001c0001t0001g0141 a0001c0001t0001g0193 a0001c0001t0001g0215 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1201-1840C>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847474 | |||||||
chr12:116847494 | T | C | 3 | a0001c0005t0020g0161 a0001c0013t0020g0098 a0001c0016t0032g0044 |
3 | HG02630.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1201-1820T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847494 | |||||||
chr12:116847532 | C | CT | 97 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(94): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1201-1770dupT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116847532 | ||||||
chr12:116847532 | CT | C | 6 | a0001c0001t0019g0124 a0001c0001t0019g0153 a0001c0001t0019g0187 others(3): Show |
6 | HG00140.hp1 HG01261.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-1770delT | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 116847532 | ||||||
chr12:116847604 | C | T | 1 | a0001c0001t0024g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1201-1710C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847604 | |||||||
chr12:116847713 | G | T | 2 | a0001c0001t0070g0068 a0001c0002t0010g0132 |
2 | HG01109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1201-1601G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847713 | |||||||
chr12:116847839 | T | A | 214 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(211): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1201-1475T>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116847839 | |||||||
chr12:116848043 | G | C | 19 | a0001c0001t0005g0104 a0001c0001t0005g0245 a0001c0001t0005g0246 others(16): Show |
19 | HG01175.hp2 HG01243.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1201-1271G>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848043 | |||||||
chr12:116848074 | T | C | 255 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(252): Show |
255 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.1201-1240T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848074 | |||||||
chr12:116848090 | T | C | 3 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0014g0158 |
3 | NA18957.hp2 NA19062.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1201-1224T>C | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848090 | |||||||
chr12:116848237 | A | G | 1 | a0001c0012t0001g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1201-1077A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848237 | |||||||
chr12:116848311 | G | A | 1 | a0001c0009t0052g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1201-1003G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848311 | |||||||
chr12:116848323 | G | A | 26 | a0001c0001t0004g0095 a0001c0001t0004g0096 a0001c0001t0004g0109 others(23): Show |
26 | HG00544.hp1 HG00673.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1201-991G>A | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848323 | |||||||
chr12:116848574 | A | G | 18 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(15): Show |
18 | HG00140.hp1 HG00741.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-740A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848574 | |||||||
chr12:116848579 | C | T | 12 | a0001c0001t0008g0026 a0001c0001t0008g0029 a0001c0001t0008g0030 others(9): Show |
12 | HG00741.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-735C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848579 | |||||||
chr12:116848619 | A | G | 1 | a0001c0002t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-695A>G | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116848619 | |||||||
chr12:116849176 | C | T | 75 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0086 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1201-138C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849176 | |||||||
chr12:116849254 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1201-60C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849254 | |||||||
chr12:116849275 | G | T | 2 | a0001c0001t0002g0210 a0002c0010t0002g0254 |
2 | HG00438.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1201-39G>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849275 | |||||||
chr12:116849307 | C | T | 3 | a0001c0001t0001g0164 a0001c0002t0001g0111 a0001c0002t0012g0014 |
3 | HG01361.hp1 HG02004.hp2 HG02148.hp2 |
splice_region_variant&intron_variant | LOW | c.1201-7C>T | RNFT2 | ENSG00000135119.15 | transcript | ENST00000257575.9 | protein_coding | 10/10 | chr12 | 116849307 |