Item | Value |
---|---|
geneid | 25914 |
ensemblid | ENSG00000176225.15 |
hgncid | 18654 |
symbol | RTTN |
name | rotatin |
refseq_nuc | NM_173630.4 |
refseq_prot | NP_775901.3 |
ensembl_nuc | ENST00000640769.2 |
ensembl_prot | ENSP00000491507.1 |
mane_status | MANE Select |
chr | chr18 |
start | 70003031 |
end | 70205687 |
strand | - |
ver | v1.2 |
region | chr18:70003031-70205687 |
region5000 | chr18:69998031-70210687 |
regionname0 | RTTN_chr18_70003031_70205687 |
regionname5000 | RTTN_chr18_69998031_70210687 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2227 | 70 | 54 | 7 | 1 | 2 | 6 | 0 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2222): Show |
chr18 | 69998031 | 70210687 |
a0002 | 0/1 | 2227 | 62 | 12 | 22 | 11 | 2 | 14 | 4 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2222): Show |
chr18 | 69998031 | 70210687 |
a0003 | 1/0 | 2226 | 20 | 17 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2221): Show |
chr18 | 69998031 | 70210687 |
a0004 | 0/0 | 2227 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2222): Show |
chr18 | 69998031 | 70210687 |
a0005 | 0/0 | 2227 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2222): Show |
chr18 | 69998031 | 70210687 |
a0006 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | MVLAG others(2222): Show |
chr18 | 69998031 | 70210687 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 6681 | 25 | 23 | 2 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0005 | 0/0 | 6681 | 11 | 11 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0006 | 0/0 | 6681 | 9 | 2 | 2 | 1 | 0 | 4 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0007 | 0/0 | 6681 | 6 | 6 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0008 | 0/0 | 6681 | 4 | 3 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0009 | 0/0 | 6681 | 3 | 0 | 0 | 0 | 1 | 2 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0010 | 0/0 | 6681 | 2 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0011 | 0/0 | 6681 | 2 | 0 | 1 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0012 | 0/0 | 6681 | 2 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0013 | 0/0 | 6681 | 2 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0021 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0022 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0023 | 0/0 | 6681 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0001c0024 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0001 | 0/1 | 6681 | 36 | 5 | 15 | 7 | 2 | 6 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0003 | 0/0 | 6681 | 21 | 6 | 6 | 3 | 0 | 6 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0016 | 0/0 | 6681 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0017 | 0/0 | 6681 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0018 | 0/0 | 6681 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0019 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0002c0020 | 0/0 | 6681 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0003c0004 | 1/0 | 6678 | 20 | 17 | 2 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6673): Show |
chr18 | 69998031 | 70210687 | ||
a0004c0025 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0004c0026 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0005c0015 | 0/0 | 6681 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 | ||
a0006c0014 | 0/0 | 6681 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | ATGGT others(6676): Show |
chr18 | 69998031 | 70210687 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 7834 | 2 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0002t0002 | 0/0 | 7833 | 20 | 18 | 2 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0002t0004 | 0/0 | 7835 | 3 | 3 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0005t0001 | 0/0 | 7834 | 5 | 5 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0005t0002 | 0/0 | 7833 | 3 | 3 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0005t0010 | 0/0 | 7833 | 2 | 2 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0005t0027 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0006t0001 | 0/0 | 7834 | 7 | 0 | 2 | 1 | 0 | 4 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0006t0020 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0006t0021 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0007t0001 | 0/0 | 7834 | 6 | 6 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0008t0008 | 0/0 | 7833 | 4 | 3 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0009t0001 | 0/0 | 7834 | 2 | 0 | 0 | 0 | 1 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0009t0004 | 0/0 | 7835 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0010t0001 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0010t0004 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0011t0004 | 0/0 | 7835 | 2 | 0 | 1 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0012t0018 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0012t0019 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0013t0015 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0001c0013t0016 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0021t0017 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0022t0004 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0001c0023t0014 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0001c0024t0012 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0001 | 0/1 | 7834 | 15 | 3 | 5 | 2 | 1 | 3 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0002 | 0/0 | 7833 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0004 | 0/0 | 7835 | 2 | 0 | 1 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0005 | 0/0 | 7834 | 7 | 0 | 3 | 4 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0007 | 0/0 | 7833 | 4 | 1 | 1 | 1 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0009 | 0/0 | 7834 | 3 | 0 | 2 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0011 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0013 | 0/0 | 7834 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0024 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0002c0001t0025 | 0/0 | 7835 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0002c0003t0001 | 0/0 | 7834 | 20 | 6 | 5 | 3 | 0 | 6 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0003t0026 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0016t0001 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0017t0002 | 0/0 | 7833 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7828): Show |
chr18 | 69998031 | 70210687 |
a0002c0018t0005 | 0/0 | 7834 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0019t0011 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0002c0020t0001 | 0/0 | 7834 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0003c0004t0002 | 1/0 | 7830 | 1 | 0 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7825): Show |
chr18 | 69998031 | 70210687 |
a0003c0004t0003 | 0/0 | 7829 | 14 | 13 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7824): Show |
chr18 | 69998031 | 70210687 |
a0003c0004t0006 | 0/0 | 7830 | 4 | 3 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7825): Show |
chr18 | 69998031 | 70210687 |
a0003c0004t0023 | 0/0 | 7829 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7824): Show |
chr18 | 69998031 | 70210687 |
a0004c0025t0001 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0004c0026t0004 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7830): Show |
chr18 | 69998031 | 70210687 |
a0005c0015t0001 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
a0006c0014t0022 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | CTCCG others(7829): Show |
chr18 | 69998031 | 70210687 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0002t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0005t0027g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0020g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0006t0021g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0008t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0008t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0008t0008g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0008t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0009t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0009t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0010t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0010t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0011t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0011t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0012t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0012t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0013t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0013t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0021t0017g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0022t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0023t0014g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0001c0024t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0009g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0009g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0024g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0001t0025g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0003t0026g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0016t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0017t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0018t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0019t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0002c0020t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0002g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0003c0004t0023g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0004c0025t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0004c0026t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0005c0015t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
a0006c0014t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0076 | EUR | GBR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00099 | hp2 | a0001 | c0011 | t0004 | g0152 | EUR | GBR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00621 | hp1 | a0002 | c0001 | t0005 | g0094 | EAS | CHS | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0098 | EAS | CHS | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00639 | hp1 | a0001 | c0011 | t0004 | g0151 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0075 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0088 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00735 | hp2 | a0002 | c0001 | t0005 | g0043 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00738 | hp1 | a0002 | c0001 | t0009 | g0099 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG00738 | hp2 | a0002 | c0001 | t0007 | g0083 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01081 | hp1 | a0002 | c0016 | t0001 | g0062 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01081 | hp2 | a0003 | c0004 | t0003 | g0009 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01106 | hp1 | a0001 | c0006 | t0001 | g0125 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0087 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01109 | hp1 | a0003 | c0004 | t0006 | g0010 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01109 | hp2 | a0002 | c0001 | t0001 | g0100 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01168 | hp1 | a0002 | c0003 | t0001 | g0048 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01168 | hp2 | a0001 | c0006 | t0001 | g0122 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01169 | hp1 | a0002 | c0003 | t0001 | g0154 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0047 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01243 | hp1 | a0001 | c0008 | t0008 | g0117 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01243 | hp2 | a0002 | c0001 | t0004 | g0077 | AMR | PUR | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01255 | hp1 | a0002 | c0001 | t0002 | g0103 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01257 | hp1 | a0005 | c0015 | t0001 | g0069 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01257 | hp2 | a0002 | c0001 | t0005 | g0082 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0089 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01361 | hp1 | a0002 | c0003 | t0026 | g0101 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01361 | hp2 | a0002 | c0001 | t0025 | g0045 | AMR | CLM | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01891 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01978 | hp1 | a0002 | c0001 | t0009 | g0090 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01978 | hp2 | a0002 | c0001 | t0005 | g0044 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG01981 | hp2 | a0002 | c0001 | t0011 | g0085 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0066 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02040 | hp2 | a0002 | c0001 | t0007 | g0059 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02055 | hp1 | a0001 | c0008 | t0008 | g0116 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02055 | hp2 | a0002 | c0001 | t0024 | g0042 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02074 | hp2 | a0001 | c0006 | t0001 | g0123 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02145 | hp1 | a0001 | c0007 | t0001 | g0146 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02257 | hp1 | a0001 | c0007 | t0001 | g0150 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02257 | hp2 | a0001 | c0008 | t0008 | g0118 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02258 | hp1 | a0001 | c0007 | t0001 | g0145 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02258 | hp2 | a0002 | c0001 | t0007 | g0061 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02280 | hp1 | a0002 | c0001 | t0001 | g0079 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02280 | hp2 | a0001 | c0010 | t0001 | g0132 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0080 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02300 | hp2 | a0001 | c0023 | t0014 | g0155 | AMR | PEL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02451 | hp1 | a0003 | c0004 | t0003 | g0021 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02523 | hp1 | a0002 | c0001 | t0005 | g0081 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | KHV | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02615 | hp1 | a0003 | c0004 | t0006 | g0014 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0147 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02630 | hp2 | a0001 | c0005 | t0002 | g0112 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02647 | hp1 | a0001 | c0007 | t0001 | g0149 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02647 | hp2 | a0001 | c0013 | t0015 | g0127 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02717 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02723 | hp1 | a0003 | c0004 | t0003 | g0002 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02723 | hp2 | a0001 | c0005 | t0001 | g0110 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02735 | hp1 | a0002 | c0003 | t0001 | g0067 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02735 | hp2 | a0001 | c0009 | t0001 | g0040 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02738 | hp1 | a0002 | c0017 | t0002 | g0102 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02738 | hp2 | a0002 | c0001 | t0004 | g0093 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02809 | hp2 | a0001 | c0021 | t0017 | g0131 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02818 | hp1 | a0001 | c0022 | t0004 | g0105 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02886 | hp1 | a0003 | c0004 | t0003 | g0011 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0056 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02895 | hp1 | a0003 | c0004 | t0003 | g0007 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0111 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02896 | hp1 | a0001 | c0012 | t0019 | g0130 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02896 | hp2 | a0001 | c0005 | t0027 | g0023 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02897 | hp1 | a0001 | c0012 | t0018 | g0128 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02897 | hp2 | a0003 | c0004 | t0003 | g0006 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02922 | hp2 | a0001 | c0005 | t0010 | g0005 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0108 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02970 | hp2 | a0003 | c0004 | t0006 | g0015 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02976 | hp1 | a0006 | c0014 | t0022 | g0046 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02976 | hp2 | a0001 | c0005 | t0002 | g0106 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03041 | hp1 | a0001 | c0008 | t0008 | g0115 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0121 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03098 | hp2 | a0001 | c0013 | t0016 | g0129 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03139 | hp1 | a0003 | c0004 | t0003 | g0013 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03139 | hp2 | a0001 | c0005 | t0002 | g0107 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0153 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0055 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03209 | hp1 | a0003 | c0004 | t0006 | g0017 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03209 | hp2 | a0001 | c0005 | t0001 | g0109 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03225 | hp2 | a0003 | c0004 | t0003 | g0020 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0054 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03239 | hp2 | a0001 | c0006 | t0001 | g0126 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03453 | hp1 | a0003 | c0004 | t0003 | g0018 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03453 | hp2 | a0001 | c0006 | t0020 | g0120 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03486 | hp1 | a0001 | c0006 | t0021 | g0119 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03486 | hp2 | a0003 | c0004 | t0023 | g0024 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0078 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03490 | hp2 | a0001 | c0006 | t0001 | g0001 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03492 | hp1 | a0002 | c0001 | t0013 | g0070 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03492 | hp2 | a0001 | c0006 | t0001 | g0001 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03516 | hp2 | a0001 | c0010 | t0004 | g0133 | AFR | ESN | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03540 | hp2 | a0001 | c0024 | t0012 | g0022 | AFR | GWD | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03579 | hp2 | a0003 | c0004 | t0003 | g0019 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0053 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0072 | SAS | PJL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03927 | hp1 | a0001 | c0009 | t0004 | g0142 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0063 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03942 | hp1 | a0002 | c0018 | t0005 | g0097 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0096 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG04184 | hp1 | a0001 | c0006 | t0001 | g0124 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0086 | SAS | BEB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0057 | AFR | YRI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18522 | hp2 | a0004 | c0025 | t0001 | g0144 | AFR | YRI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18906 | hp1 | a0003 | c0004 | t0003 | g0012 | AFR | YRI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | YRI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18948 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18948 | hp2 | a0002 | c0001 | t0005 | g0051 | EAS | JPT | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18971 | hp1 | a0002 | c0001 | t0005 | g0074 | EAS | JPT | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA18971 | hp2 | a0002 | c0020 | t0001 | g0071 | EAS | JPT | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20129 | hp1 | a0002 | c0001 | t0001 | g0073 | AFR | ASW | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20129 | hp2 | a0003 | c0004 | t0003 | g0008 | AFR | ASW | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20805 | hp1 | a0001 | c0009 | t0001 | g0039 | EUR | TSI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20805 | hp2 | a0002 | c0001 | t0009 | g0091 | EUR | TSI | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0064 | SAS | GIH | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20905 | hp2 | a0002 | c0001 | t0007 | g0060 | SAS | GIH | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02109 | hp1 | a0002 | c0003 | t0001 | g0068 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02559 | hp1 | a0001 | c0005 | t0010 | g0004 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03471 | hp1 | a0003 | c0004 | t0003 | g0016 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG03471 | hp2 | a0001 | c0007 | t0001 | g0148 | AFR | MSL | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG06807 | hp1 | a0002 | c0019 | t0011 | g0058 | AFR | USA | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | USA | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20300 | hp1 | a0002 | c0001 | t0001 | g0104 | AFR | USA | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | USA | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA21309 | hp1 | a0004 | c0026 | t0004 | g0143 | AFR | LWK | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | LWK | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0092 | REF | REF | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
homoSapiens | grch38p0 | a0003 | c0004 | t0002 | g0114 | REF | REF | RTTN_chr18_69998031_70210687 | RTTN | chr18 | 69998031 | 70210687 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:70006461 | C | T | 1 | a0002 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.6445G>A | p.Ala2149Thr | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/49 | 6474/7830 | 6445/6681 | 2149/2226 | chr18 | 70006461 | |||
chr18:70051452 | A | G | 5 | a0001 a0002 a0004 others(2): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
missense_variant | MODERATE | c.5282T>C | p.Phe1761Ser | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/49 | 5311/7830 | 5282/6681 | 1761/2226 | chr18 | 70051452 | |||
chr18:70054256 | G | C | 2 | a0001 a0002 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.5060C>G | p.Ser1687Cys | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/49 | 5089/7830 | 5060/6681 | 1687/2226 | chr18 | 70054256 | |||
chr18:70059940 | A | G | 1 | a0001 | 5 | HG02647.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.4850T>C | p.Met1617Thr | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/49 | 4879/7830 | 4850/6681 | 1617/2226 | chr18 | 70059940 | |||
chr18:70086668 | T | C | 1 | a0002 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.4319A>G | p.Gln1440Arg | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/49 | 4348/7830 | 4319/6681 | 1440/2226 | chr18 | 70086668 | |||
chr18:70114547 | T | C | 1 | a0006 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.3581A>G | p.Glu1194Gly | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/49 | 3610/7830 | 3581/6681 | 1194/2226 | chr18 | 70114547 | |||
chr18:70121573 | C | T | 1 | a0001 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.3511G>A | p.Glu1171Lys | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/49 | 3540/7830 | 3511/6681 | 1171/2226 | chr18 | 70121573 | |||
chr18:70135254 | T | C | 1 | a0001 | 4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
missense_variant | MODERATE | c.2815A>G | p.Ser939Gly | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/49 | 2844/7830 | 2815/6681 | 939/2226 | chr18 | 70135254 | |||
chr18:70166070 | T | C | 1 | a0001 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1921A>G | p.Ile641Val | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/49 | 1950/7830 | 1921/6681 | 641/2226 | chr18 | 70166070 | |||
chr18:70166180 | G | A | 1 | a0001 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1811C>T | p.Ser604Phe | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/49 | 1840/7830 | 1811/6681 | 604/2226 | chr18 | 70166180 | |||
chr18:70168879 | G | T | 2 | a0001 a0002 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.1665C>A | p.Asn555Lys | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/49 | 1694/7830 | 1665/6681 | 555/2226 | chr18 | 70168879 | |||
chr18:70176821 | C | T | 1 | a0001 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1330G>A | p.Gly444Arg | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/49 | 1359/7830 | 1330/6681 | 444/2226 | chr18 | 70176821 | |||
chr18:70196608 | T | C | 2 | a0001 a0006 |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(26): Show |
missense_variant | MODERATE | c.734A>G | p.Lys245Arg | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/49 | 763/7830 | 734/6681 | 245/2226 | chr18 | 70196608 | |||
chr18:70196614 | T | TCTC | 5 | a0001 a0002 a0004 others(2): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
conservative_inframe_insertion | MODERATE | c.725_727dupGAG | p.Gly242dup | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/49 | 756/7830 | 727/6681 | 243/2226 | chr18 | 70196614 | |||
chr18:70199459 | A | T | 1 | a0005 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.533T>A | p.Leu178Gln | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/49 | 562/7830 | 533/6681 | 178/2226 | chr18 | 70199459 | |||
chr18:70204107 | A | C | 3 | a0002 a0004 a0005 |
64 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
missense_variant | MODERATE | c.376T>G | p.Ser126Ala | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/49 | 405/7830 | 376/6681 | 126/2226 | chr18 | 70204107 | |||
chr18:70204256 | G | A | 1 | a0004 | 2 | NA18522.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.227C>T | p.Pro76Leu | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/49 | 256/7830 | 227/6681 | 76/2226 | chr18 | 70204256 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:70004196 | A | G | 2 | a0004c0025 a0004c0026 |
2 | NA18522.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.6636T>C | p.Tyr2212Tyr | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 6665/7830 | 6636/6681 | 2212/2226 | chr18 | 70004196 | |||
chr18:70020624 | T | C | 3 | a0001c0009 a0002c0003 a0002c0016 |
25 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
synonymous_variant | LOW | c.6144A>G | p.Val2048Val | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/49 | 6173/7830 | 6144/6681 | 2048/2226 | chr18 | 70020624 | |||
chr18:70020753 | G | A | 1 | a0001c0023 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.6015C>T | p.Ala2005Ala | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/49 | 6044/7830 | 6015/6681 | 2005/2226 | chr18 | 70020753 | |||
chr18:70020777 | A | G | 1 | a0004c0025 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.5991T>C | p.Pro1997Pro | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/49 | 6020/7830 | 5991/6681 | 1997/2226 | chr18 | 70020777 | |||
chr18:70024789 | C | T | 1 | a0001c0024 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.5883G>A | p.Leu1961Leu | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/49 | 5912/7830 | 5883/6681 | 1961/2226 | chr18 | 70024789 | |||
chr18:70051415 | C | G | 1 | a0002c0018 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.5319G>C | p.Ala1773Ala | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/49 | 5348/7830 | 5319/6681 | 1773/2226 | chr18 | 70051415 | |||
chr18:70057781 | C | G | 2 | a0004c0025 a0004c0026 |
2 | NA18522.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.4992G>C | p.Leu1664Leu | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/49 | 5021/7830 | 4992/6681 | 1664/2226 | chr18 | 70057781 | |||
chr18:70109639 | C | T | 1 | a0001c0022 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.3762G>A | p.Ala1254Ala | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/49 | 3791/7830 | 3762/6681 | 1254/2226 | chr18 | 70109639 | |||
chr18:70128498 | G | A | 1 | a0006c0014 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.3003C>T | p.Tyr1001Tyr | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/49 | 3032/7830 | 3003/6681 | 1001/2226 | chr18 | 70128498 | |||
chr18:70166149 | T | C | 2 | a0001c0011 a0002c0017 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.1842A>G | p.Glu614Glu | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/49 | 1871/7830 | 1842/6681 | 614/2226 | chr18 | 70166149 | |||
chr18:70176693 | C | T | 1 | a0001c0010 | 2 | HG02280.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1458G>A | p.Thr486Thr | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/49 | 1487/7830 | 1458/6681 | 486/2226 | chr18 | 70176693 | |||
chr18:70197681 | A | G | 1 | a0002c0016 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.636T>C | p.Asp212Asp | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/49 | 665/7830 | 636/6681 | 212/2226 | chr18 | 70197681 | |||
chr18:70205164 | C | T | 1 | a0006c0014 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.183G>A | p.Lys61Lys | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/49 | 212/7830 | 183/6681 | 61/2226 | chr18 | 70205164 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:70003081 | C | T | 1 | a0001c0008t0008 | 4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1070G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 1070 | chr18 | 70003081 | ||||||
chr18:70003111 | A | T | 2 | a0001c0006t0020 a0001c0006t0021 |
2 | HG03453.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1040T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 1040 | chr18 | 70003111 | ||||||
chr18:70003120 | T | A | 4 | a0002c0001t0005 a0002c0001t0024 a0002c0001t0025 others(1): Show |
10 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1031A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 1031 | chr18 | 70003120 | ||||||
chr18:70003368 | T | A | 1 | a0001c0023t0014 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*783A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 783 | chr18 | 70003368 | ||||||
chr18:70003369 | C | T | 1 | a0001c0023t0014 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 782 | chr18 | 70003369 | ||||||
chr18:70003382 | T | G | 1 | a0002c0001t0009 | 3 | HG00738.hp1 HG01978.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*769A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 769 | chr18 | 70003382 | ||||||
chr18:70003509 | G | A | 2 | a0001c0006t0020 a0001c0006t0021 |
2 | HG03453.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*642C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 642 | chr18 | 70003509 | ||||||
chr18:70003509 | G | T | 1 | a0006c0014t0022 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 642 | chr18 | 70003509 | ||||||
chr18:70003524 | A | G | 6 | a0001c0006t0020 a0001c0006t0021 a0001c0012t0018 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*627T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 627 | chr18 | 70003524 | ||||||
chr18:70003527 | A | C | 2 | a0001c0021t0017 a0001c0024t0012 |
2 | HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*624T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 624 | chr18 | 70003527 | ||||||
chr18:70003532 | C | G | 2 | a0001c0013t0015 a0001c0013t0016 |
2 | HG02647.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*619G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 619 | chr18 | 70003532 | ||||||
chr18:70003601 | C | T | 1 | a0001c0023t0014 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 550 | chr18 | 70003601 | ||||||
chr18:70003626 | G | C | 1 | a0002c0003t0026 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*525C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 525 | chr18 | 70003626 | ||||||
chr18:70003629 | T | C | 2 | a0001c0005t0010 a0001c0005t0027 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*522A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 522 | chr18 | 70003629 | ||||||
chr18:70003924 | A | G | 1 | a0002c0001t0013 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 227 | chr18 | 70003924 | ||||||
chr18:70004058 | C | T | 3 | a0002c0001t0007 a0002c0001t0011 a0002c0019t0011 |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*93G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 49/49 | 93 | chr18 | 70004058 | ||||||
chr18:70205677 | A | C | 4 | a0001c0005t0010 a0001c0024t0012 a0003c0004t0003 others(1): Show |
21 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-19T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/49 | 19 | chr18 | 70205677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:70004296 | G | A | 3 | a0004c0025t0001g0144 a0004c0026t0004g0143 a0006c0014t0022g0046 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6596-60C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004296 | |||||||
chr18:70004351 | T | C | 1 | a0003c0004t0003g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6596-115A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004351 | |||||||
chr18:70004420 | C | T | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.6596-184G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004420 | |||||||
chr18:70004509 | T | C | 133 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.6596-273A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004509 | |||||||
chr18:70004514 | T | C | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6596-278A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004514 | |||||||
chr18:70004552 | T | A | 3 | a0004c0025t0001g0144 a0004c0026t0004g0143 a0006c0014t0022g0046 |
3 | HG02976.hp1 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6596-316A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004552 | |||||||
chr18:70004656 | C | G | 4 | a0002c0001t0001g0073 a0002c0001t0001g0095 a0002c0001t0004g0077 others(1): Show |
4 | HG01243.hp2 HG01981.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.6596-420G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004656 | |||||||
chr18:70004670 | T | A | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6596-434A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004670 | |||||||
chr18:70004722 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.6595+476G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004722 | |||||||
chr18:70004869 | TA | T | 80 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.6595+328delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004869 | |||||||
chr18:70004903 | T | C | 88 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.6595+295A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004903 | |||||||
chr18:70004977 | A | G | 2 | a0002c0001t0001g0076 a0002c0001t0004g0093 |
2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.6595+221T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70004977 | |||||||
chr18:70005029 | CATCT | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6595+165_6595+168d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70005029 | |||||||
chr18:70005060 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6595+138A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70005060 | |||||||
chr18:70005100 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.6595+98A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70005100 | |||||||
chr18:70005132 | A | G | 1 | a0002c0003t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6595+66T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 48/48 | chr18 | 70005132 | |||||||
chr18:70005515 | T | C | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.6526-248A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70005515 | |||||||
chr18:70005656 | A | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6526-389T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70005656 | |||||||
chr18:70005695 | C | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.6526-428G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70005695 | |||||||
chr18:70005788 | A | C | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6526-521T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70005788 | |||||||
chr18:70005873 | T | C | 1 | a0002c0019t0011g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6525+508A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70005873 | |||||||
chr18:70006030 | AC | A | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6525+350delG | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70006030 | |||||||
chr18:70006056 | G | C | 1 | a0002c0001t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6525+325C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70006056 | |||||||
chr18:70006230 | G | T | 3 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 |
3 | HG02723.hp2 HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.6525+151C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70006230 | |||||||
chr18:70006314 | A | G | 4 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0018 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.6525+67T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70006314 | |||||||
chr18:70006350 | C | G | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.6525+31G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 47/48 | chr18 | 70006350 | |||||||
chr18:70006691 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.6422-207C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70006691 | |||||||
chr18:70006813 | A | G | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6422-329T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70006813 | |||||||
chr18:70006980 | A | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6422-496T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70006980 | |||||||
chr18:70007030 | G | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6422-546C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007030 | |||||||
chr18:70007109 | C | A | 7 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0023t0014g0155 others(4): Show |
7 | HG00099.hp2 HG00639.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.6422-625G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007109 | |||||||
chr18:70007188 | C | G | 1 | a0002c0001t0013g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6422-704G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007188 | |||||||
chr18:70007210 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.6422-726C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007210 | |||||||
chr18:70007237 | C | T | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6422-753G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007237 | |||||||
chr18:70007349 | G | A | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6422-865C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007349 | |||||||
chr18:70007452 | T | C | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.6422-968A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007452 | |||||||
chr18:70007575 | G | A | 6 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 others(3): Show |
6 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.6422-1091C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007575 | |||||||
chr18:70007630 | G | T | 6 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 others(3): Show |
6 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.6422-1146C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007630 | |||||||
chr18:70007876 | G | A | 72 | a0001c0002t0002g0140 a0001c0006t0001g0001 a0001c0006t0001g0122 others(69): Show |
73 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.6422-1392C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007876 | |||||||
chr18:70007984 | T | C | 92 | a0001c0002t0002g0140 a0001c0006t0001g0001 a0001c0006t0001g0122 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.6422-1500A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70007984 | |||||||
chr18:70008302 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6422-1818G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70008302 | |||||||
chr18:70008706 | GA | G | 18 | a0001c0005t0001g0141 a0003c0004t0003g0006 a0003c0004t0003g0007 others(15): Show |
18 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.6422-2223delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70008706 | |||||||
chr18:70008770 | C | A | 89 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.6422-2286G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70008770 | |||||||
chr18:70009179 | G | C | 10 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0051 others(7): Show |
10 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6422-2695C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009179 | |||||||
chr18:70009378 | C | T | 1 | a0001c0008t0008g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6422-2894G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009378 | |||||||
chr18:70009379 | G | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6422-2895C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009379 | |||||||
chr18:70009425 | T | C | 132 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.6422-2941A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009425 | |||||||
chr18:70009652 | C | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6422-3168G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009652 | |||||||
chr18:70009750 | C | T | 1 | a0002c0001t0001g0084 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6422-3266G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009750 | |||||||
chr18:70009800 | G | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6422-3316C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70009800 | |||||||
chr18:70010006 | A | G | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6422-3522T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70010006 | |||||||
chr18:70010122 | G | A | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6422-3638C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70010122 | |||||||
chr18:70010333 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6422-3849C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70010333 | |||||||
chr18:70010400 | A | G | 89 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.6422-3916T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70010400 | |||||||
chr18:70010701 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6422-4217A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70010701 | |||||||
chr18:70011021 | T | C | 2 | a0002c0003t0001g0048 a0002c0003t0001g0154 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.6422-4537A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011021 | |||||||
chr18:70011047 | G | A | 1 | a0002c0001t0004g0077 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6422-4563C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011047 | |||||||
chr18:70011154 | G | C | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.6422-4670C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011154 | |||||||
chr18:70011161 | A | G | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.6422-4677T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011161 | |||||||
chr18:70011194 | T | C | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6422-4710A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011194 | |||||||
chr18:70011489 | C | T | 1 | a0001c0008t0008g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6422-5005G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011489 | |||||||
chr18:70011541 | T | C | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6422-5057A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011541 | |||||||
chr18:70011618 | C | T | 2 | a0001c0009t0001g0039 a0001c0009t0001g0040 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.6422-5134G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011618 | |||||||
chr18:70011762 | T | TA | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6422-5279dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011762 | |||||||
chr18:70011882 | A | G | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.6422-5398T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011882 | |||||||
chr18:70011898 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6422-5414C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011898 | |||||||
chr18:70011905 | G | A | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6422-5421C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011905 | |||||||
chr18:70011966 | G | A | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6421+5441C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011966 | |||||||
chr18:70011987 | A | T | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6421+5420T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70011987 | |||||||
chr18:70012019 | C | G | 89 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.6421+5388G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012019 | |||||||
chr18:70012054 | G | T | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6421+5353C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012054 | |||||||
chr18:70012059 | G | A | 1 | a0002c0001t0007g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6421+5348C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012059 | |||||||
chr18:70012090 | A | G | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6421+5317T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012090 | |||||||
chr18:70012198 | T | A | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6421+5209A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012198 | |||||||
chr18:70012431 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6421+4976A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012431 | |||||||
chr18:70012491 | T | C | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6421+4916A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012491 | |||||||
chr18:70012507 | T | C | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.6421+4900A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012507 | |||||||
chr18:70012553 | C | T | 1 | a0002c0003t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6421+4854G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012553 | |||||||
chr18:70012632 | T | G | 2 | a0002c0001t0005g0043 a0002c0001t0024g0042 |
2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.6421+4775A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012632 | |||||||
chr18:70012633 | A | G | 91 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.6421+4774T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012633 | |||||||
chr18:70012659 | G | A | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.6421+4748C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012659 | |||||||
chr18:70012708 | C | T | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6421+4699G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012708 | |||||||
chr18:70012774 | T | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6421+4633A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012774 | |||||||
chr18:70012872 | GA | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6421+4534delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70012872 | |||||||
chr18:70013126 | G | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6421+4281C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013126 | |||||||
chr18:70013369 | C | CTGTGTGT others(43): Show |
5 | a0003c0004t0003g0012 a0003c0004t0003g0013 a0003c0004t0003g0016 others(2): Show |
5 | HG03139.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.6421+4037_6421+403 others(54): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013369 | |||||||
chr18:70013369 | C | CTGTGTGT others(45): Show |
14 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(11): Show |
14 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.6421+3986_6421+403 others(56): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013369 | |||||||
chr18:70013391 | A | AT | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.6421+4015dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013391 | |||||||
chr18:70013393 | ATG | A | 3 | a0002c0001t0011g0085 a0004c0025t0001g0144 a0004c0026t0004g0143 |
3 | HG01981.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6421+4012_6421+401 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013393 | |||||||
chr18:70013413 | C | CTG | 2 | a0002c0020t0001g0071 a0006c0014t0022g0046 |
2 | HG02976.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.6421+3992_6421+399 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013413 | |||||||
chr18:70013413 | C | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6421+3994G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013413 | |||||||
chr18:70013413 | CTG | C | 3 | a0001c0002t0002g0027 a0001c0002t0002g0034 a0001c0023t0014g0155 |
3 | HG01884.hp2 HG02300.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.6421+3992_6421+399 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013413 | |||||||
chr18:70013414 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+3993A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013414 | |||||||
chr18:70013806 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+3601T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013806 | |||||||
chr18:70013877 | C | T | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6421+3530G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013877 | |||||||
chr18:70013887 | A | G | 1 | a0001c0002t0002g0027 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6421+3520T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70013887 | |||||||
chr18:70014049 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.6421+3358C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70014049 | |||||||
chr18:70014792 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6421+2615C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70014792 | |||||||
chr18:70014792 | G | GT | 2 | a0002c0001t0005g0082 a0005c0015t0001g0069 |
2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.6421+2614dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70014792 | |||||||
chr18:70015082 | C | CT | 18 | a0001c0005t0001g0113 a0001c0005t0002g0112 a0001c0006t0020g0120 others(15): Show |
18 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.6421+2324dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015082 | |||||||
chr18:70015142 | G | A | 2 | a0002c0001t0009g0091 a0002c0001t0009g0099 |
2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.6421+2265C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015142 | |||||||
chr18:70015515 | C | T | 8 | a0002c0003t0001g0047 a0002c0003t0001g0048 a0002c0003t0001g0050 others(5): Show |
8 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.6421+1892G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015515 | |||||||
chr18:70015520 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+1887C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015520 | |||||||
chr18:70015606 | A | G | 1 | a0003c0004t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6421+1801T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015606 | |||||||
chr18:70015619 | C | T | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.6421+1788G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015619 | |||||||
chr18:70015651 | CAA | C | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6421+1754_6421+175 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015651 | |||||||
chr18:70015744 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6421+1663A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015744 | |||||||
chr18:70015828 | T | C | 109 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.6421+1579A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015828 | |||||||
chr18:70015833 | GA | G | 132 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.6421+1573delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015833 | |||||||
chr18:70015928 | C | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6421+1479G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015928 | |||||||
chr18:70015976 | T | C | 5 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.6421+1431A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70015976 | |||||||
chr18:70016051 | C | T | 1 | a0002c0001t0005g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6421+1356G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016051 | |||||||
chr18:70016075 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+1332C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016075 | |||||||
chr18:70016124 | A | T | 1 | a0002c0001t0009g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6421+1283T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016124 | |||||||
chr18:70016181 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+1226A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016181 | |||||||
chr18:70016216 | AAT | A | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.6421+1189_6421+119 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016216 | |||||||
chr18:70016237 | G | A | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.6421+1170C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016237 | |||||||
chr18:70016251 | C | T | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6421+1156G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016251 | |||||||
chr18:70016356 | C | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.6421+1051G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016356 | |||||||
chr18:70016430 | G | A | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6421+977C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016430 | |||||||
chr18:70016462 | C | T | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.6421+945G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016462 | |||||||
chr18:70016479 | A | G | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.6421+928T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016479 | |||||||
chr18:70016584 | C | T | 24 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 others(21): Show |
24 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.6421+823G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016584 | |||||||
chr18:70016671 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6421+736C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016671 | |||||||
chr18:70016696 | G | T | 36 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(33): Show |
36 | HG01081.hp2 HG01109.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.6421+711C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70016696 | |||||||
chr18:70017039 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6421+368G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70017039 | |||||||
chr18:70017249 | G | C | 3 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 |
3 | HG02970.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.6421+158C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 46/48 | chr18 | 70017249 | |||||||
chr18:70017771 | C | T | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.6154-97G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70017771 | |||||||
chr18:70017793 | T | C | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.6154-119A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70017793 | |||||||
chr18:70017889 | T | A | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.6154-215A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70017889 | |||||||
chr18:70018092 | T | C | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.6154-418A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018092 | |||||||
chr18:70018108 | A | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.6154-434T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018108 | |||||||
chr18:70018189 | TCATTA | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6154-520_6154-516d others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018189 | |||||||
chr18:70018243 | T | A | 2 | a0002c0003t0001g0063 a0002c0003t0001g0086 |
2 | HG03927.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.6154-569A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018243 | |||||||
chr18:70018466 | T | G | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.6154-792A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018466 | |||||||
chr18:70018488 | T | TTC | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6154-816_6154-815d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018488 | |||||||
chr18:70018826 | CT | C | 83 | a0001c0002t0002g0025 a0001c0002t0002g0135 a0001c0002t0002g0136 others(80): Show |
84 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.6154-1153delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018826 | |||||||
chr18:70018826 | CTT | C | 8 | a0001c0002t0004g0121 a0001c0002t0004g0153 a0001c0005t0001g0109 others(5): Show |
8 | HG01081.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.6154-1154_6154-115 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018826 | |||||||
chr18:70018923 | GA | G | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.6154-1250delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70018923 | |||||||
chr18:70019164 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.6153+1451A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70019164 | |||||||
chr18:70019354 | A | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6153+1261T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70019354 | |||||||
chr18:70019399 | T | G | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.6153+1216A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70019399 | |||||||
chr18:70019448 | G | A | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.6153+1167C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70019448 | |||||||
chr18:70019497 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6153+1118A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70019497 | |||||||
chr18:70020001 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6153+614C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020001 | |||||||
chr18:70020023 | G | T | 70 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(67): Show |
71 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.6153+592C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020023 | |||||||
chr18:70020088 | A | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.6153+527T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020088 | |||||||
chr18:70020108 | A | C | 84 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(81): Show |
85 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.6153+507T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020108 | |||||||
chr18:70020117 | C | G | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.6153+498G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020117 | |||||||
chr18:70020409 | A | G | 16 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(13): Show |
16 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.6153+206T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020409 | |||||||
chr18:70020473 | A | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6153+142T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 45/48 | chr18 | 70020473 | |||||||
chr18:70020874 | A | G | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5951-57T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70020874 | |||||||
chr18:70021374 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5951-557A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70021374 | |||||||
chr18:70021835 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5951-1018A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70021835 | |||||||
chr18:70022283 | A | AT | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5951-1467dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70022283 | |||||||
chr18:70022333 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5951-1516A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70022333 | |||||||
chr18:70022720 | T | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5951-1903A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70022720 | |||||||
chr18:70022940 | G | A | 1 | a0002c0003t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5950+1782C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70022940 | |||||||
chr18:70022965 | T | C | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5950+1757A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70022965 | |||||||
chr18:70023057 | CT | C | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5950+1664delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70023057 | |||||||
chr18:70023367 | G | T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5950+1355C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70023367 | |||||||
chr18:70023451 | T | C | 1 | a0001c0006t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5950+1271A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70023451 | |||||||
chr18:70023837 | T | C | 1 | a0001c0002t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5950+885A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70023837 | |||||||
chr18:70023957 | G | A | 20 | a0001c0023t0014g0155 a0003c0004t0003g0002 a0003c0004t0003g0003 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.5950+765C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70023957 | |||||||
chr18:70024284 | A | C | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5950+438T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70024284 | |||||||
chr18:70024512 | G | A | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5950+210C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70024512 | |||||||
chr18:70024584 | C | T | 6 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(3): Show |
6 | HG01255.hp2 HG02145.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5950+138G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70024584 | |||||||
chr18:70024685 | T | G | 10 | a0001c0005t0001g0141 a0001c0006t0020g0120 a0001c0006t0021g0119 others(7): Show |
10 | HG02615.hp2 HG02647.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.5950+37A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 44/48 | chr18 | 70024685 | |||||||
chr18:70024987 | C | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5824-139G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70024987 | |||||||
chr18:70025096 | T | C | 4 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(1): Show |
4 | HG02895.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.5824-248A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025096 | |||||||
chr18:70025238 | C | T | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5824-390G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025238 | |||||||
chr18:70025486 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.5824-638G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025486 | |||||||
chr18:70025592 | G | A | 1 | a0001c0006t0001g0122 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5824-744C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025592 | |||||||
chr18:70025689 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5824-841C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025689 | |||||||
chr18:70025805 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5824-957C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025805 | |||||||
chr18:70025827 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5824-979T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70025827 | |||||||
chr18:70026174 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5824-1326C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70026174 | |||||||
chr18:70026264 | G | T | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5824-1416C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70026264 | |||||||
chr18:70026627 | T | C | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5824-1779A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70026627 | |||||||
chr18:70027021 | T | C | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5823+1703A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027021 | |||||||
chr18:70027072 | A | C | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5823+1652T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027072 | |||||||
chr18:70027416 | C | A | 2 | a0002c0001t0011g0085 a0002c0019t0011g0058 |
2 | HG01981.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5823+1308G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027416 | |||||||
chr18:70027451 | G | A | 1 | a0001c0002t0004g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5823+1273C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027451 | |||||||
chr18:70027553 | C | T | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5823+1171G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027553 | |||||||
chr18:70027587 | G | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5823+1137C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70027587 | |||||||
chr18:70028041 | G | T | 1 | a0002c0001t0007g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5823+683C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028041 | |||||||
chr18:70028059 | A | C | 4 | a0002c0003t0001g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5823+665T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028059 | |||||||
chr18:70028083 | G | T | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5823+641C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028083 | |||||||
chr18:70028269 | G | A | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5823+455C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028269 | |||||||
chr18:70028345 | C | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5823+379G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028345 | |||||||
chr18:70028400 | T | C | 1 | a0001c0006t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5823+324A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028400 | |||||||
chr18:70028520 | G | A | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5823+204C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028520 | |||||||
chr18:70028637 | AT | A | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.5823+86delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 43/48 | chr18 | 70028637 | |||||||
chr18:70029078 | G | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5746-277C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029078 | |||||||
chr18:70029163 | CA | C | 86 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5746-363delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029163 | |||||||
chr18:70029621 | A | T | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5745+391T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029621 | |||||||
chr18:70029807 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5745+205A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029807 | |||||||
chr18:70029977 | CTATA | C | 5 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5745+31_5745+34del others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029977 | |||||||
chr18:70029999 | C | A | 1 | a0002c0003t0026g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5745+13G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 42/48 | chr18 | 70029999 | |||||||
chr18:70030196 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5648-87C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 41/48 | chr18 | 70030196 | |||||||
chr18:70030233 | T | C | 1 | a0001c0002t0002g0135 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5648-124A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 41/48 | chr18 | 70030233 | |||||||
chr18:70030860 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5647+16C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 41/48 | chr18 | 70030860 | |||||||
chr18:70031069 | G | C | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-88C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031069 | |||||||
chr18:70031324 | A | C | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5542-343T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031324 | |||||||
chr18:70031337 | G | A | 2 | a0003c0004t0003g0009 a0003c0004t0003g0021 |
2 | HG01081.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.5542-356C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031337 | |||||||
chr18:70031499 | T | C | 89 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.5542-518A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031499 | |||||||
chr18:70031673 | T | A | 126 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.5542-692A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031673 | |||||||
chr18:70031824 | A | C | 1 | a0001c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5542-843T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031824 | |||||||
chr18:70031857 | C | T | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-876G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031857 | |||||||
chr18:70031858 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5542-877A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031858 | |||||||
chr18:70031984 | A | G | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5542-1003T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70031984 | |||||||
chr18:70032106 | T | C | 106 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(103): Show |
107 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.5542-1125A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032106 | |||||||
chr18:70032147 | T | C | 24 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0002c0003t0001g0047 others(21): Show |
24 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.5542-1166A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032147 | |||||||
chr18:70032173 | G | A | 1 | a0002c0001t0007g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5542-1192C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032173 | |||||||
chr18:70032182 | C | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-1201G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032182 | |||||||
chr18:70032238 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-1257A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032238 | |||||||
chr18:70032277 | G | C | 1 | a0001c0005t0002g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5542-1296C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032277 | |||||||
chr18:70032354 | T | C | 35 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(32): Show |
35 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(32): Show |
intron_variant | MODIFIER | c.5542-1373A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032354 | |||||||
chr18:70032417 | G | A | 1 | a0002c0003t0001g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5542-1436C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032417 | |||||||
chr18:70032504 | A | G | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5542-1523T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032504 | |||||||
chr18:70032523 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5542-1542A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032523 | |||||||
chr18:70032563 | A | G | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5542-1582T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032563 | |||||||
chr18:70032569 | A | T | 1 | a0002c0003t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5542-1588T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032569 | |||||||
chr18:70032592 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5542-1611G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032592 | |||||||
chr18:70032619 | G | A | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.5542-1638C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032619 | |||||||
chr18:70032676 | A | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-1695T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032676 | |||||||
chr18:70032944 | G | A | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5542-1963C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032944 | |||||||
chr18:70032957 | A | T | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5542-1976T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70032957 | |||||||
chr18:70033112 | G | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5542-2131C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033112 | |||||||
chr18:70033387 | C | T | 132 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.5542-2406G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033387 | |||||||
chr18:70033717 | C | T | 2 | a0002c0003t0001g0048 a0002c0003t0001g0154 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5542-2736G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033717 | |||||||
chr18:70033762 | A | C | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5542-2781T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033762 | |||||||
chr18:70033856 | T | TAATACAA others(11): Show |
77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-2876_5542-287 others(22): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033856 | |||||||
chr18:70033910 | A | C | 126 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.5542-2929T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70033910 | |||||||
chr18:70034164 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5542-3183G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034164 | |||||||
chr18:70034203 | T | C | 1 | a0001c0006t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5542-3222A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034203 | |||||||
chr18:70034239 | CAG | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-3260_5542-325 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034239 | |||||||
chr18:70034347 | T | C | 2 | a0002c0001t0001g0078 a0005c0015t0001g0069 |
2 | HG01257.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.5542-3366A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034347 | |||||||
chr18:70034475 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5542-3494G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034475 | |||||||
chr18:70034553 | C | T | 1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5542-3572G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034553 | |||||||
chr18:70034650 | T | C | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-3669A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034650 | |||||||
chr18:70034653 | T | C | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5542-3672A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034653 | |||||||
chr18:70034674 | G | A | 1 | a0002c0001t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5542-3693C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034674 | |||||||
chr18:70034907 | C | T | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5542-3926G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034907 | |||||||
chr18:70034931 | T | C | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5542-3950A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034931 | |||||||
chr18:70034974 | A | T | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-3993T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70034974 | |||||||
chr18:70035173 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5542-4192G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035173 | |||||||
chr18:70035211 | C | T | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5542-4230G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035211 | |||||||
chr18:70035250 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5542-4269C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035250 | |||||||
chr18:70035319 | A | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5542-4338T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035319 | |||||||
chr18:70035350 | A | G | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-4369T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035350 | |||||||
chr18:70035684 | G | C | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5542-4703C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035684 | |||||||
chr18:70035742 | C | A | 1 | a0002c0001t0005g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5542-4761G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035742 | |||||||
chr18:70035830 | C | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5542-4849G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035830 | |||||||
chr18:70035871 | C | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-4890G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035871 | |||||||
chr18:70035956 | C | T | 1 | a0003c0004t0003g0002 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5542-4975G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70035956 | |||||||
chr18:70036021 | A | G | 17 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(14): Show |
18 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.5542-5040T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70036021 | |||||||
chr18:70036054 | C | T | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5542-5073G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70036054 | |||||||
chr18:70036127 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5542-5146C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70036127 | |||||||
chr18:70036518 | G | C | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-5537C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70036518 | |||||||
chr18:70036850 | C | G | 16 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(13): Show |
17 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5542-5869G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70036850 | |||||||
chr18:70037353 | A | G | 1 | a0002c0001t0001g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.5542-6372T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70037353 | |||||||
chr18:70037713 | T | C | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5542-6732A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70037713 | |||||||
chr18:70037895 | A | T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5542-6914T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70037895 | |||||||
chr18:70037897 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.5542-6916G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70037897 | |||||||
chr18:70037998 | TGGTGGCC others(4): Show |
T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5542-7028_5542-701 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70037998 | |||||||
chr18:70038048 | C | G | 3 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 |
3 | HG02723.hp2 HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.5542-7067G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70038048 | |||||||
chr18:70038184 | A | G | 77 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(74): Show |
78 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.5542-7203T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70038184 | |||||||
chr18:70038246 | T | A | 2 | a0001c0006t0001g0125 a0002c0001t0001g0100 |
2 | HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.5542-7265A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70038246 | |||||||
chr18:70038364 | G | A | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5542-7383C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70038364 | |||||||
chr18:70038702 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5542-7721C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70038702 | |||||||
chr18:70039005 | G | T | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5542-8024C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039005 | |||||||
chr18:70039088 | C | T | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5542-8107G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039088 | |||||||
chr18:70039398 | T | C | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5542-8417A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039398 | |||||||
chr18:70039408 | A | G | 1 | a0002c0003t0026g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5542-8427T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039408 | |||||||
chr18:70039459 | G | A | 5 | a0002c0003t0001g0063 a0002c0003t0001g0086 a0002c0003t0001g0087 others(2): Show |
5 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.5542-8478C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039459 | |||||||
chr18:70039460 | A | G | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5542-8479T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039460 | |||||||
chr18:70039473 | T | G | 71 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(68): Show |
72 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.5542-8492A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039473 | |||||||
chr18:70039494 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5541+8477T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039494 | |||||||
chr18:70039507 | C | G | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5541+8464G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039507 | |||||||
chr18:70039553 | T | C | 1 | a0002c0001t0001g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5541+8418A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039553 | |||||||
chr18:70039646 | C | T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5541+8325G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039646 | |||||||
chr18:70039702 | T | A | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5541+8269A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039702 | |||||||
chr18:70039724 | A | G | 2 | a0001c0005t0002g0106 a0001c0005t0002g0107 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5541+8247T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039724 | |||||||
chr18:70039819 | G | A | 1 | a0005c0015t0001g0069 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5541+8152C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70039819 | |||||||
chr18:70040038 | A | C | 1 | a0002c0001t0009g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5541+7933T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040038 | |||||||
chr18:70040053 | A | AAAG | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5541+7915_5541+791 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040053 | |||||||
chr18:70040164 | A | G | 28 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(25): Show |
28 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.5541+7807T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040164 | |||||||
chr18:70040254 | T | C | 78 | a0001c0002t0002g0137 a0001c0006t0001g0001 a0001c0006t0001g0122 others(75): Show |
79 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.5541+7717A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040254 | |||||||
chr18:70040304 | C | CA | 85 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(82): Show |
86 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.5541+7666dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040304 | |||||||
chr18:70040457 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5541+7514C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040457 | |||||||
chr18:70040513 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5541+7458C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040513 | |||||||
chr18:70040572 | A | C | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5541+7399T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040572 | |||||||
chr18:70040621 | C | A | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5541+7350G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040621 | |||||||
chr18:70040703 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5541+7268A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040703 | |||||||
chr18:70040913 | A | G | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5541+7058T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70040913 | |||||||
chr18:70041251 | TA | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5541+6719delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041251 | |||||||
chr18:70041280 | A | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5541+6691T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041280 | |||||||
chr18:70041316 | T | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.5541+6655A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041316 | |||||||
chr18:70041380 | G | GCA | 85 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(82): Show |
86 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.5541+6589_5541+659 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041380 | |||||||
chr18:70041380 | G | GCACACA | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5541+6585_5541+659 others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041380 | |||||||
chr18:70041380 | GCA | G | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5541+6589_5541+659 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041380 | |||||||
chr18:70041466 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.5541+6505G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041466 | |||||||
chr18:70041467 | T | C | 1 | a0003c0004t0006g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5541+6504A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041467 | |||||||
chr18:70041699 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5541+6272A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041699 | |||||||
chr18:70041882 | A | G | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.5541+6089T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041882 | |||||||
chr18:70041907 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5541+6064G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041907 | |||||||
chr18:70041931 | C | T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5541+6040G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70041931 | |||||||
chr18:70042026 | T | C | 16 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(13): Show |
17 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5541+5945A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042026 | |||||||
chr18:70042086 | T | C | 5 | a0002c0003t0001g0049 a0002c0003t0001g0052 a0002c0003t0001g0055 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5541+5885A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042086 | |||||||
chr18:70042120 | G | GA | 11 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(8): Show |
12 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.5541+5850dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042120 | |||||||
chr18:70042120 | GAAA | G | 5 | a0002c0001t0005g0051 a0002c0001t0005g0074 a0002c0001t0005g0081 others(2): Show |
5 | HG00621.hp1 HG02523.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.5541+5848_5541+585 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042120 | |||||||
chr18:70042229 | A | G | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5541+5742T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042229 | |||||||
chr18:70042366 | C | CT | 28 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0037 others(25): Show |
28 | HG00099.hp1 HG00621.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.5541+5604dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042366 | C | CTT | 15 | a0001c0006t0001g0001 a0001c0006t0001g0123 a0001c0006t0020g0120 others(12): Show |
16 | HG01109.hp1 HG01109.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.5541+5603_5541+560 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042366 | C | CTTT | 7 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0019 others(4): Show |
7 | HG01081.hp2 HG02615.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.5541+5602_5541+560 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042366 | CT | C | 11 | a0001c0005t0001g0141 a0001c0005t0002g0106 a0001c0005t0002g0107 others(8): Show |
11 | HG01169.hp1 HG01257.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.5541+5604delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042366 | CTTTTTT | C | 5 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5541+5599_5541+560 others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042366 | CTTTTTTT others(3): Show |
C | 1 | a0003c0004t0003g0006 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5541+5595_5541+560 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042366 | |||||||
chr18:70042372 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5541+5599A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042372 | |||||||
chr18:70042382 | TTTTTTTT others(5): Show |
T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5541+5577_5541+558 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042382 | |||||||
chr18:70042394 | G | T | 9 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(6): Show |
10 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.5541+5577C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042394 | |||||||
chr18:70042440 | A | T | 1 | a0002c0003t0001g0047 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.5541+5531T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042440 | |||||||
chr18:70042469 | G | A | 13 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(10): Show |
14 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.5541+5502C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042469 | |||||||
chr18:70042520 | T | C | 1 | a0002c0003t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5541+5451A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042520 | |||||||
chr18:70042525 | G | A | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5541+5446C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042525 | |||||||
chr18:70042576 | C | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5541+5395G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042576 | |||||||
chr18:70042579 | T | C | 1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5541+5392A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042579 | |||||||
chr18:70042628 | A | G | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5541+5343T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042628 | |||||||
chr18:70042656 | A | G | 5 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.5541+5315T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042656 | |||||||
chr18:70042853 | T | C | 1 | a0002c0001t0001g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5541+5118A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042853 | |||||||
chr18:70042948 | C | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5541+5023G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70042948 | |||||||
chr18:70043068 | G | C | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.5541+4903C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043068 | |||||||
chr18:70043105 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5541+4866C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043105 | |||||||
chr18:70043158 | A | G | 68 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(65): Show |
68 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.5541+4813T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043158 | |||||||
chr18:70043291 | A | G | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.5541+4680T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043291 | |||||||
chr18:70043351 | A | G | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5541+4620T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043351 | |||||||
chr18:70043498 | T | C | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5541+4473A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043498 | |||||||
chr18:70043552 | A | C | 1 | a0001c0002t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5541+4419T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043552 | |||||||
chr18:70043734 | G | T | 3 | a0002c0001t0001g0073 a0002c0001t0001g0095 a0002c0001t0004g0077 |
3 | HG01243.hp2 HG01981.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5541+4237C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043734 | |||||||
chr18:70043751 | T | C | 134 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.5541+4220A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043751 | |||||||
chr18:70043778 | C | A | 1 | a0002c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.5541+4193G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70043778 | |||||||
chr18:70044006 | A | G | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5541+3965T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044006 | |||||||
chr18:70044126 | A | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5541+3845T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044126 | |||||||
chr18:70044197 | T | C | 83 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(80): Show |
84 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.5541+3774A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044197 | |||||||
chr18:70044424 | T | C | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5541+3547A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044424 | |||||||
chr18:70044649 | T | C | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5541+3322A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044649 | |||||||
chr18:70044745 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5541+3226A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044745 | |||||||
chr18:70044869 | C | T | 68 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(65): Show |
69 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.5541+3102G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044869 | |||||||
chr18:70044952 | C | T | 2 | a0001c0005t0010g0004 a0001c0005t0010g0005 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5541+3019G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044952 | |||||||
chr18:70044974 | C | T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5541+2997G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70044974 | |||||||
chr18:70045072 | T | C | 1 | a0002c0003t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5541+2899A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70045072 | |||||||
chr18:70045193 | T | C | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5541+2778A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70045193 | |||||||
chr18:70045292 | T | C | 1 | a0002c0001t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5541+2679A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70045292 | |||||||
chr18:70045758 | A | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5541+2213T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70045758 | |||||||
chr18:70045878 | G | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5541+2093C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70045878 | |||||||
chr18:70046057 | A | AT | 19 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(16): Show |
20 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.5541+1913dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046057 | |||||||
chr18:70046072 | C | T | 1 | a0001c0006t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5541+1899G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046072 | |||||||
chr18:70046073 | G | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5541+1898C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046073 | |||||||
chr18:70046093 | T | G | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.5541+1878A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046093 | |||||||
chr18:70046106 | T | C | 1 | a0002c0001t0009g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5541+1865A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046106 | |||||||
chr18:70046327 | C | A | 16 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(13): Show |
17 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5541+1644G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046327 | |||||||
chr18:70046501 | T | C | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5541+1470A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046501 | |||||||
chr18:70046668 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5541+1303C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046668 | |||||||
chr18:70046773 | G | A | 4 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG03225.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5541+1198C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70046773 | |||||||
chr18:70047037 | A | G | 1 | a0002c0001t0007g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5541+934T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047037 | |||||||
chr18:70047059 | A | G | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5541+912T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047059 | |||||||
chr18:70047071 | A | C | 1 | a0002c0001t0007g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5541+900T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047071 | |||||||
chr18:70047087 | A | G | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5541+884T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047087 | |||||||
chr18:70047155 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5541+816A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047155 | |||||||
chr18:70047168 | C | T | 1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5541+803G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047168 | |||||||
chr18:70047373 | C | A | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5541+598G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047373 | |||||||
chr18:70047581 | A | C | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5541+390T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047581 | |||||||
chr18:70047955 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5541+16G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 40/48 | chr18 | 70047955 | |||||||
chr18:70048210 | T | C | 1 | a0002c0003t0001g0050 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5324-22A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048210 | |||||||
chr18:70048448 | T | G | 1 | a0001c0007t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5324-260A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048448 | |||||||
chr18:70048484 | G | A | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5324-296C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048484 | |||||||
chr18:70048596 | A | G | 1 | a0002c0001t0007g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5324-408T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048596 | |||||||
chr18:70048597 | TTTTG | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.5324-413_5324-410d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048597 | |||||||
chr18:70048646 | C | A | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5324-458G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048646 | |||||||
chr18:70048773 | G | A | 1 | a0002c0003t0001g0050 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5324-585C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048773 | |||||||
chr18:70048818 | C | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.5324-630G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70048818 | |||||||
chr18:70049002 | C | T | 17 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.5324-814G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049002 | |||||||
chr18:70049072 | A | T | 1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5324-884T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049072 | |||||||
chr18:70049355 | G | A | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5324-1167C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049355 | |||||||
chr18:70049378 | C | T | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.5324-1190G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049378 | |||||||
chr18:70049445 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5324-1257T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049445 | |||||||
chr18:70049462 | C | T | 3 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 |
3 | HG02970.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5324-1274G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049462 | |||||||
chr18:70049541 | A | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5324-1353T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049541 | |||||||
chr18:70049687 | T | C | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5324-1499A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049687 | |||||||
chr18:70049882 | T | C | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5323+1529A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049882 | |||||||
chr18:70049896 | G | T | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5323+1515C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049896 | |||||||
chr18:70049967 | T | C | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5323+1444A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70049967 | |||||||
chr18:70050024 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5323+1387A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050024 | |||||||
chr18:70050424 | A | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5323+987T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050424 | |||||||
chr18:70050451 | G | A | 144 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.5323+960C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050451 | |||||||
chr18:70050625 | T | TATGTTTA others(3): Show |
1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5323+776_5323+785d others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050625 | |||||||
chr18:70050779 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.5323+632C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050779 | |||||||
chr18:70050787 | C | T | 1 | a0001c0009t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5323+624G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050787 | |||||||
chr18:70050844 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5323+567A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050844 | |||||||
chr18:70050995 | T | G | 19 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(16): Show |
20 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.5323+416A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70050995 | |||||||
chr18:70051005 | A | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5323+406T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70051005 | |||||||
chr18:70051015 | C | G | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5323+396G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70051015 | |||||||
chr18:70051108 | T | C | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5323+303A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70051108 | |||||||
chr18:70051365 | G | A | 1 | a0002c0003t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.5323+46C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 39/48 | chr18 | 70051365 | |||||||
chr18:70051552 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.5186-4A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70051552 | |||||||
chr18:70051601 | C | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5186-53G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70051601 | |||||||
chr18:70051700 | A | C | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5186-152T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70051700 | |||||||
chr18:70052084 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5186-536T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052084 | |||||||
chr18:70052112 | G | A | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.5186-564C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052112 | |||||||
chr18:70052282 | A | C | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5186-734T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052282 | |||||||
chr18:70052316 | C | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5186-768G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052316 | |||||||
chr18:70052348 | T | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.5186-800A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052348 | |||||||
chr18:70052387 | G | A | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5186-839C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052387 | |||||||
chr18:70052459 | A | G | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.5186-911T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052459 | |||||||
chr18:70052642 | T | TTA | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.5186-1096_5186-109 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052642 | |||||||
chr18:70052642 | T | TTATATAT others(1): Show |
7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5186-1102_5186-109 others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052642 | |||||||
chr18:70052642 | T | TTATATAT others(3): Show |
30 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(27): Show |
31 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.5186-1104_5186-109 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052642 | |||||||
chr18:70052642 | T | TTATATAT others(5): Show |
33 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(30): Show |
33 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.5186-1106_5186-109 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052642 | |||||||
chr18:70052642 | T | TTATATAT others(7): Show |
2 | a0002c0001t0005g0082 a0002c0018t0005g0097 |
2 | HG01257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.5186-1095_5186-109 others(18): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052642 | |||||||
chr18:70052650 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5186-1102T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052650 | |||||||
chr18:70052651 | T | TATATATA others(5): Show |
1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5186-1104_5186-110 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052651 | |||||||
chr18:70052698 | AT | A | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5186-1151delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052698 | |||||||
chr18:70052774 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5186-1226G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052774 | |||||||
chr18:70052858 | A | G | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5185+1273T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052858 | |||||||
chr18:70052859 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5185+1272A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052859 | |||||||
chr18:70052892 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5185+1239C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052892 | |||||||
chr18:70052998 | T | C | 7 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.5185+1133A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70052998 | |||||||
chr18:70053010 | A | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5185+1121T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053010 | |||||||
chr18:70053018 | G | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.5185+1113C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053018 | |||||||
chr18:70053122 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5185+1009A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053122 | |||||||
chr18:70053170 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5185+961C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053170 | |||||||
chr18:70053422 | T | G | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.5185+709A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053422 | |||||||
chr18:70053771 | G | T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.5185+360C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053771 | |||||||
chr18:70053803 | T | C | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.5185+328A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70053803 | |||||||
chr18:70054045 | A | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.5185+86T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70054045 | |||||||
chr18:70054104 | A | G | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5185+27T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 38/48 | chr18 | 70054104 | |||||||
chr18:70054479 | C | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5032-195G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054479 | |||||||
chr18:70054515 | A | C | 83 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(80): Show |
84 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.5032-231T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054515 | |||||||
chr18:70054567 | A | G | 1 | a0002c0003t0001g0050 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5032-283T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054567 | |||||||
chr18:70054615 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5032-331A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054615 | |||||||
chr18:70054653 | T | C | 123 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.5032-369A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054653 | |||||||
chr18:70054689 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5032-405G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054689 | |||||||
chr18:70054970 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5032-686C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70054970 | |||||||
chr18:70055046 | T | A | 122 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(120): Show |
intron_variant | MODIFIER | c.5032-762A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055046 | |||||||
chr18:70055209 | G | A | 1 | a0001c0006t0021g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5032-925C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055209 | |||||||
chr18:70055318 | TAC | T | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5032-1036_5032-103 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055318 | |||||||
chr18:70055318 | TACACACA others(1): Show |
T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5032-1042_5032-103 others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055318 | |||||||
chr18:70055467 | TCTC | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5032-1186_5032-118 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055467 | |||||||
chr18:70055517 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5032-1233T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055517 | |||||||
chr18:70055524 | T | C | 68 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(65): Show |
69 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.5032-1240A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055524 | |||||||
chr18:70055583 | C | T | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5032-1299G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055583 | |||||||
chr18:70055781 | C | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.5032-1497G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055781 | |||||||
chr18:70055882 | T | C | 1 | a0002c0003t0001g0050 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5032-1598A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70055882 | |||||||
chr18:70056126 | C | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5031+1616G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70056126 | |||||||
chr18:70056245 | C | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5031+1497G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70056245 | |||||||
chr18:70056886 | A | G | 1 | a0001c0002t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5031+856T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70056886 | |||||||
chr18:70057351 | T | C | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5031+391A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70057351 | |||||||
chr18:70057566 | A | G | 74 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(71): Show |
75 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.5031+176T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70057566 | |||||||
chr18:70057604 | G | C | 16 | a0002c0003t0001g0047 a0002c0003t0001g0048 a0002c0003t0001g0050 others(13): Show |
16 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.5031+138C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70057604 | |||||||
chr18:70057634 | T | C | 1 | a0003c0004t0003g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5031+108A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 37/48 | chr18 | 70057634 | |||||||
chr18:70057903 | A | C | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.4941-71T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70057903 | |||||||
chr18:70057953 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4941-121A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70057953 | |||||||
chr18:70057972 | T | C | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.4941-140A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70057972 | |||||||
chr18:70058062 | C | T | 54 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0135 others(51): Show |
54 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.4941-230G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058062 | |||||||
chr18:70058137 | T | C | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4941-305A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058137 | |||||||
chr18:70058346 | G | A | 5 | a0001c0002t0002g0025 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG01255.hp2 HG01891.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4941-514C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058346 | |||||||
chr18:70058433 | G | A | 6 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4941-601C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058433 | |||||||
chr18:70058467 | G | T | 2 | a0001c0012t0018g0128 a0001c0012t0019g0130 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4941-635C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058467 | |||||||
chr18:70058484 | T | C | 42 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0135 others(39): Show |
42 | HG01081.hp2 HG01109.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.4941-652A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058484 | |||||||
chr18:70058513 | C | T | 128 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0135 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.4941-681G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058513 | |||||||
chr18:70058679 | G | A | 43 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(40): Show |
43 | HG01081.hp2 HG01109.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.4941-847C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058679 | |||||||
chr18:70058796 | T | TA | 16 | a0002c0001t0001g0072 a0002c0001t0001g0075 a0002c0001t0001g0076 others(13): Show |
16 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.4941-965dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058796 | |||||||
chr18:70058924 | C | T | 129 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.4940+926G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70058924 | |||||||
chr18:70059025 | G | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4940+825C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70059025 | |||||||
chr18:70059739 | A | G | 62 | a0001c0022t0004g0105 a0002c0001t0001g0072 a0002c0001t0001g0073 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.4940+111T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70059739 | |||||||
chr18:70059767 | A | T | 134 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.4940+83T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70059767 | |||||||
chr18:70059769 | A | G | 1 | a0001c0006t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4940+81T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70059769 | |||||||
chr18:70059843 | C | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.4940+7G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 36/48 | chr18 | 70059843 | |||||||
chr18:70060047 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4748-5A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060047 | |||||||
chr18:70060095 | A | T | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.4748-53T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060095 | |||||||
chr18:70060112 | T | C | 18 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.4748-70A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060112 | |||||||
chr18:70060252 | A | T | 12 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(9): Show |
13 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.4748-210T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060252 | |||||||
chr18:70060371 | C | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4748-329G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060371 | |||||||
chr18:70060430 | C | T | 144 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.4748-388G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060430 | |||||||
chr18:70060466 | A | C | 15 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(12): Show |
16 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.4748-424T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060466 | |||||||
chr18:70060705 | T | C | 1 | a0001c0007t0001g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4748-663A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060705 | |||||||
chr18:70060781 | C | A | 2 | a0002c0003t0001g0047 a0002c0003t0001g0053 |
2 | HG01169.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.4748-739G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060781 | |||||||
chr18:70060781 | C | T | 2 | a0001c0012t0018g0128 a0001c0012t0019g0130 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4748-739G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060781 | |||||||
chr18:70060820 | T | G | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4748-778A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060820 | |||||||
chr18:70060837 | A | G | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4748-795T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060837 | |||||||
chr18:70060966 | AT | A | 43 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(40): Show |
43 | HG01081.hp2 HG01109.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.4748-925delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060966 | |||||||
chr18:70060969 | T | A | 43 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(40): Show |
43 | HG01081.hp2 HG01109.hp1 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.4748-927A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70060969 | |||||||
chr18:70061212 | C | A | 1 | a0002c0001t0009g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4748-1170G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061212 | |||||||
chr18:70061271 | C | T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4748-1229G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061271 | |||||||
chr18:70061293 | C | T | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4748-1251G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061293 | |||||||
chr18:70061560 | A | G | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.4748-1518T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061560 | |||||||
chr18:70061673 | A | C | 1 | a0001c0002t0002g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4748-1631T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061673 | |||||||
chr18:70061857 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4748-1815T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70061857 | |||||||
chr18:70062003 | C | T | 7 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.4748-1961G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062003 | |||||||
chr18:70062048 | C | T | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4748-2006G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062048 | |||||||
chr18:70062097 | A | T | 129 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.4748-2055T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062097 | |||||||
chr18:70062303 | G | T | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4748-2261C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062303 | |||||||
chr18:70062459 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4748-2417G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062459 | |||||||
chr18:70062476 | C | T | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.4748-2434G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062476 | |||||||
chr18:70062626 | TTC | T | 80 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(77): Show |
80 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.4748-2586_4748-258 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062626 | |||||||
chr18:70062627 | TC | T | 38 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0007t0001g0145 others(35): Show |
38 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.4748-2586delG | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062627 | |||||||
chr18:70062628 | C | T | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.4748-2586G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062628 | |||||||
chr18:70062649 | A | T | 19 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(16): Show |
20 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.4748-2607T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062649 | |||||||
chr18:70062851 | C | T | 10 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0051 others(7): Show |
10 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4748-2809G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70062851 | |||||||
chr18:70063155 | AGTTTT | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4747+2669_4747+267 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063155 | |||||||
chr18:70063319 | T | G | 18 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.4747+2510A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063319 | |||||||
chr18:70063613 | A | G | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4747+2216T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063613 | |||||||
chr18:70063622 | A | AT | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4747+2206dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063622 | |||||||
chr18:70063889 | T | C | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4747+1940A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063889 | |||||||
chr18:70063965 | C | CT | 97 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(94): Show |
97 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.4747+1863dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063965 | |||||||
chr18:70063965 | C | CTT | 7 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(4): Show |
7 | HG02451.hp2 HG02723.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.4747+1862_4747+186 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063965 | |||||||
chr18:70063965 | C | CTTTT | 6 | a0001c0006t0001g0122 a0001c0012t0018g0128 a0001c0012t0019g0130 others(3): Show |
6 | HG01168.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4747+1860_4747+186 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063965 | |||||||
chr18:70063965 | C | CTTTTT | 12 | a0001c0006t0001g0001 a0001c0006t0001g0123 a0001c0006t0001g0124 others(9): Show |
13 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.4747+1859_4747+186 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70063965 | |||||||
chr18:70064048 | C | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4747+1781G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064048 | |||||||
chr18:70064125 | G | T | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.4747+1704C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064125 | |||||||
chr18:70064203 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4747+1626G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064203 | |||||||
chr18:70064336 | C | CA | 12 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(9): Show |
12 | HG01243.hp1 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.4747+1492dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064336 | |||||||
chr18:70064336 | CA | C | 77 | a0001c0002t0002g0038 a0001c0002t0004g0108 a0001c0002t0004g0121 others(74): Show |
78 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.4747+1492delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064336 | |||||||
chr18:70064336 | CAA | C | 11 | a0001c0024t0012g0022 a0003c0004t0003g0006 a0003c0004t0003g0007 others(8): Show |
11 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.4747+1491_4747+149 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064336 | |||||||
chr18:70064475 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4747+1354T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064475 | |||||||
chr18:70064661 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4747+1168A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064661 | |||||||
chr18:70064704 | G | C | 15 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(12): Show |
15 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.4747+1125C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064704 | |||||||
chr18:70064725 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4747+1104A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70064725 | |||||||
chr18:70065122 | A | G | 67 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(64): Show |
67 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.4747+707T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065122 | |||||||
chr18:70065147 | T | C | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4747+682A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065147 | |||||||
chr18:70065270 | T | TA | 12 | a0001c0005t0002g0107 a0002c0001t0005g0043 a0002c0001t0005g0044 others(9): Show |
12 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4747+558dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065270 | |||||||
chr18:70065270 | T | TAA | 42 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(39): Show |
42 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.4747+557_4747+558d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065270 | |||||||
chr18:70065270 | T | TAAA | 25 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(22): Show |
26 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.4747+556_4747+558d others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065270 | |||||||
chr18:70065270 | T | TAAAA | 5 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(2): Show |
5 | HG00621.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4747+555_4747+558d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 35/48 | chr18 | 70065270 | |||||||
chr18:70065958 | A | G | 1 | a0001c0013t0015g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4654-36T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70065958 | |||||||
chr18:70065973 | A | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4654-51T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70065973 | |||||||
chr18:70065998 | T | A | 67 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(64): Show |
67 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.4654-76A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70065998 | |||||||
chr18:70066097 | T | A | 1 | a0001c0006t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4654-175A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066097 | |||||||
chr18:70066246 | A | G | 19 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(16): Show |
20 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.4654-324T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066246 | |||||||
chr18:70066459 | C | T | 1 | a0005c0015t0001g0069 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4654-537G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066459 | |||||||
chr18:70066519 | C | T | 1 | a0002c0003t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4654-597G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066519 | |||||||
chr18:70066547 | G | A | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.4654-625C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066547 | |||||||
chr18:70066669 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-747A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70066669 | |||||||
chr18:70067000 | G | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1078C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067000 | |||||||
chr18:70067013 | A | G | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1091T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067013 | |||||||
chr18:70067023 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1101A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067023 | |||||||
chr18:70067138 | A | G | 18 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1216T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067138 | |||||||
chr18:70067163 | A | AT | 79 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(76): Show |
80 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.4654-1242dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067163 | |||||||
chr18:70067163 | A | ATT | 6 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0003t0001g0054 others(3): Show |
6 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4654-1243_4654-124 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067163 | |||||||
chr18:70067207 | T | C | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4654-1285A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067207 | |||||||
chr18:70067246 | G | A | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4654-1324C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067246 | |||||||
chr18:70067285 | G | A | 62 | a0001c0022t0004g0105 a0002c0001t0001g0072 a0002c0001t0001g0073 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.4654-1363C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067285 | |||||||
chr18:70067321 | G | A | 1 | a0001c0005t0027g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4654-1399C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067321 | |||||||
chr18:70067330 | T | C | 1 | a0001c0002t0002g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4654-1408A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067330 | |||||||
chr18:70067402 | G | A | 18 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1480C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067402 | |||||||
chr18:70067405 | C | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4654-1483G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067405 | |||||||
chr18:70067406 | G | A | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4654-1484C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067406 | |||||||
chr18:70067411 | T | G | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4654-1489A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067411 | |||||||
chr18:70067449 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4654-1527C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067449 | |||||||
chr18:70067450 | C | T | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4654-1528G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067450 | |||||||
chr18:70067509 | T | C | 3 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 |
3 | HG02723.hp2 HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4654-1587A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067509 | |||||||
chr18:70067590 | A | G | 18 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(15): Show |
19 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.4654-1668T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067590 | |||||||
chr18:70067762 | C | T | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.4654-1840G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067762 | |||||||
chr18:70067777 | C | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4654-1855G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067777 | |||||||
chr18:70067785 | G | A | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4654-1863C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067785 | |||||||
chr18:70067785 | G | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4654-1863C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067785 | |||||||
chr18:70067968 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4654-2046A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70067968 | |||||||
chr18:70068365 | C | A | 1 | a0001c0009t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4654-2443G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068365 | |||||||
chr18:70068439 | G | A | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4654-2517C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068439 | |||||||
chr18:70068542 | G | T | 1 | a0001c0002t0004g0108 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4654-2620C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068542 | |||||||
chr18:70068543 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4654-2621G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068543 | |||||||
chr18:70068544 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4654-2622C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068544 | |||||||
chr18:70068738 | T | C | 68 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(65): Show |
69 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.4654-2816A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068738 | |||||||
chr18:70068925 | C | A | 1 | a0002c0001t0005g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4654-3003G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068925 | |||||||
chr18:70068947 | T | TGCTA | 20 | a0001c0023t0014g0155 a0003c0004t0003g0002 a0003c0004t0003g0003 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.4654-3029_4654-302 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70068947 | |||||||
chr18:70069095 | C | G | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4654-3173G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069095 | |||||||
chr18:70069288 | G | A | 12 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(9): Show |
12 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.4654-3366C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069288 | |||||||
chr18:70069305 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4654-3383A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069305 | |||||||
chr18:70069500 | A | T | 1 | a0001c0002t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4654-3578T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069500 | |||||||
chr18:70069554 | C | T | 107 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(104): Show |
108 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.4654-3632G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069554 | |||||||
chr18:70069639 | G | C | 1 | a0001c0002t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4654-3717C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70069639 | |||||||
chr18:70070011 | C | T | 1 | a0002c0001t0001g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4653+3895G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070011 | |||||||
chr18:70070136 | T | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4653+3770A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070136 | |||||||
chr18:70070148 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4653+3758G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070148 | |||||||
chr18:70070240 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4653+3666T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070240 | |||||||
chr18:70070245 | G | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4653+3661C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070245 | |||||||
chr18:70070450 | T | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4653+3456A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070450 | |||||||
chr18:70070587 | T | C | 2 | a0003c0004t0003g0009 a0003c0004t0003g0021 |
2 | HG01081.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.4653+3319A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070587 | |||||||
chr18:70070691 | A | G | 68 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(65): Show |
69 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.4653+3215T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070691 | |||||||
chr18:70070710 | C | T | 1 | a0003c0004t0006g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4653+3196G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070710 | |||||||
chr18:70070730 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4653+3176G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070730 | |||||||
chr18:70070739 | C | T | 9 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.4653+3167G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070739 | |||||||
chr18:70070801 | T | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4653+3105A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070801 | |||||||
chr18:70070934 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4653+2972C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70070934 | |||||||
chr18:70071052 | A | G | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4653+2854T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70071052 | |||||||
chr18:70071869 | C | T | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4653+2037G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70071869 | |||||||
chr18:70071911 | A | C | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.4653+1995T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70071911 | |||||||
chr18:70072130 | T | C | 4 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG03225.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4653+1776A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70072130 | |||||||
chr18:70072132 | G | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4653+1774C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70072132 | |||||||
chr18:70072562 | A | C | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4653+1344T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70072562 | |||||||
chr18:70072705 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4653+1201T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70072705 | |||||||
chr18:70072892 | G | A | 2 | a0002c0001t0009g0091 a0002c0001t0009g0099 |
2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4653+1014C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70072892 | |||||||
chr18:70073018 | A | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4653+888T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073018 | |||||||
chr18:70073365 | C | T | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.4653+541G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073365 | |||||||
chr18:70073378 | C | A | 1 | a0003c0004t0006g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4653+528G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073378 | |||||||
chr18:70073581 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4653+325G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073581 | |||||||
chr18:70073701 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4653+205C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073701 | |||||||
chr18:70073718 | A | G | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4653+188T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073718 | |||||||
chr18:70073881 | G | A | 67 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(64): Show |
67 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.4653+25C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 34/48 | chr18 | 70073881 | |||||||
chr18:70074073 | G | A | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.4565-79C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074073 | |||||||
chr18:70074119 | G | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4565-125C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074119 | |||||||
chr18:70074141 | TA | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4565-148delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074141 | |||||||
chr18:70074142 | A | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4565-148T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074142 | |||||||
chr18:70074254 | G | C | 61 | a0001c0022t0004g0105 a0002c0001t0001g0072 a0002c0001t0001g0073 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4565-260C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074254 | |||||||
chr18:70074573 | TAC | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4565-581_4565-580d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074573 | |||||||
chr18:70074602 | T | A | 91 | a0001c0005t0001g0141 a0001c0006t0001g0001 a0001c0006t0001g0122 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.4565-608A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074602 | |||||||
chr18:70074812 | A | G | 1 | a0002c0001t0005g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4564+540T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074812 | |||||||
chr18:70074996 | C | T | 86 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.4564+356G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70074996 | |||||||
chr18:70075035 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4564+317A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70075035 | |||||||
chr18:70075143 | A | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4564+209T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70075143 | |||||||
chr18:70075210 | T | C | 4 | a0002c0001t0001g0073 a0002c0001t0001g0095 a0002c0001t0004g0077 others(1): Show |
4 | HG01243.hp2 HG01981.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.4564+142A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70075210 | |||||||
chr18:70075295 | AAC | A | 3 | a0002c0003t0001g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 |
3 | HG02451.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4564+55_4564+56del others(2): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 33/48 | chr18 | 70075295 | |||||||
chr18:70075565 | G | A | 111 | a0001c0005t0001g0141 a0001c0006t0001g0001 a0001c0006t0001g0122 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.4375-24C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70075565 | |||||||
chr18:70075630 | A | G | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4375-89T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70075630 | |||||||
chr18:70075866 | T | C | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4375-325A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70075866 | |||||||
chr18:70076064 | C | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4375-523G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076064 | |||||||
chr18:70076067 | A | G | 15 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4375-526T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076067 | |||||||
chr18:70076067 | A | T | 1 | a0002c0001t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4375-526T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076067 | |||||||
chr18:70076666 | C | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4375-1125G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076666 | |||||||
chr18:70076677 | C | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4375-1136G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076677 | |||||||
chr18:70076718 | G | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4375-1177C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076718 | |||||||
chr18:70076740 | C | T | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.4375-1199G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076740 | |||||||
chr18:70076741 | G | A | 20 | a0001c0023t0014g0155 a0003c0004t0003g0002 a0003c0004t0003g0003 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.4375-1200C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076741 | |||||||
chr18:70076845 | G | C | 1 | a0003c0004t0003g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4375-1304C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076845 | |||||||
chr18:70076853 | C | T | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4375-1312G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076853 | |||||||
chr18:70076911 | C | CAG | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.4375-1372_4375-137 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076911 | |||||||
chr18:70076977 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.4375-1436G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70076977 | |||||||
chr18:70077059 | G | C | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.4375-1518C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077059 | |||||||
chr18:70077299 | C | T | 1 | a0002c0001t0009g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4375-1758G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077299 | |||||||
chr18:70077308 | A | G | 1 | a0001c0005t0010g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4375-1767T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077308 | |||||||
chr18:70077478 | G | C | 1 | a0002c0001t0005g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4375-1937C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077478 | |||||||
chr18:70077704 | T | C | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375-2163A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077704 | |||||||
chr18:70077828 | G | T | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.4375-2287C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70077828 | |||||||
chr18:70078122 | T | G | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4375-2581A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078122 | |||||||
chr18:70078129 | A | C | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.4375-2588T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078129 | |||||||
chr18:70078187 | TA | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.4375-2647delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078187 | |||||||
chr18:70078359 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4375-2818T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078359 | |||||||
chr18:70078575 | A | G | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4375-3034T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078575 | |||||||
chr18:70078582 | C | A | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.4375-3041G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078582 | |||||||
chr18:70078601 | A | T | 3 | a0002c0001t0009g0090 a0002c0001t0009g0091 a0002c0001t0009g0099 |
3 | HG00738.hp1 HG01978.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4375-3060T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078601 | |||||||
chr18:70078665 | G | A | 2 | a0003c0004t0003g0006 a0003c0004t0003g0007 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4375-3124C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078665 | |||||||
chr18:70078785 | C | T | 2 | a0001c0012t0018g0128 a0001c0012t0019g0130 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4375-3244G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078785 | |||||||
chr18:70078888 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.4375-3347G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078888 | |||||||
chr18:70078930 | G | A | 1 | a0001c0009t0001g0039 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4375-3389C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70078930 | |||||||
chr18:70079032 | A | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4375-3491T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70079032 | |||||||
chr18:70079048 | G | C | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.4375-3507C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70079048 | |||||||
chr18:70079063 | T | C | 67 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(64): Show |
68 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.4375-3522A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70079063 | |||||||
chr18:70079318 | T | A | 1 | a0002c0001t0013g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4375-3777A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70079318 | |||||||
chr18:70079720 | C | A | 1 | a0002c0003t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4375-4179G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70079720 | |||||||
chr18:70080118 | C | CATATT | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.4375-4578_4375-457 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080118 | |||||||
chr18:70080191 | T | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4375-4650A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080191 | |||||||
chr18:70080248 | T | C | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.4375-4707A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080248 | |||||||
chr18:70080479 | T | C | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4375-4938A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080479 | |||||||
chr18:70080545 | C | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.4375-5004G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080545 | |||||||
chr18:70080802 | G | T | 92 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.4375-5261C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080802 | |||||||
chr18:70080902 | G | A | 1 | a0002c0001t0001g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4375-5361C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080902 | |||||||
chr18:70080928 | T | TCA | 7 | a0001c0002t0001g0035 a0001c0002t0002g0029 a0001c0002t0002g0031 others(4): Show |
7 | HG02738.hp1 HG02922.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.4375-5389_4375-538 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | T | TCACA | 4 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0041 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4375-5391_4375-538 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | T | TCACACAC others(1): Show |
3 | a0001c0002t0002g0030 a0001c0002t0002g0034 a0001c0009t0001g0040 |
3 | HG02717.hp2 HG02735.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4375-5395_4375-538 others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCA | T | 9 | a0001c0002t0002g0028 a0001c0002t0002g0140 a0001c0002t0004g0121 others(6): Show |
9 | HG02559.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4375-5389_4375-538 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACA | T | 6 | a0001c0002t0001g0139 a0001c0002t0004g0108 a0001c0005t0001g0109 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.4375-5391_4375-538 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACA | T | 15 | a0001c0002t0002g0036 a0001c0005t0001g0113 a0001c0005t0002g0106 others(12): Show |
15 | HG01346.hp2 HG01891.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.4375-5393_4375-538 others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACAC others(1): Show |
T | 21 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(18): Show |
22 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.4375-5395_4375-538 others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACAC others(3): Show |
T | 45 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0002c0001t0001g0073 others(42): Show |
45 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4375-5397_4375-538 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACAC others(5): Show |
T | 10 | a0001c0005t0001g0141 a0001c0007t0001g0145 a0001c0007t0001g0146 others(7): Show |
10 | HG01168.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.4375-5399_4375-538 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACAC others(9): Show |
T | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4375-5403_4375-538 others(20): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080928 | TCACACAC others(13): Show |
T | 1 | a0001c0008t0008g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4375-5407_4375-538 others(24): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080928 | |||||||
chr18:70080932 | A | T | 1 | a0001c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4375-5391T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080932 | |||||||
chr18:70080934 | A | T | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4375-5393T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080934 | |||||||
chr18:70080942 | A | T | 7 | a0001c0005t0001g0141 a0001c0007t0001g0145 a0001c0007t0001g0146 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.4375-5401T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70080942 | |||||||
chr18:70081190 | G | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4374+5423C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70081190 | |||||||
chr18:70081235 | G | T | 2 | a0001c0007t0001g0147 a0001c0007t0001g0149 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4374+5378C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70081235 | |||||||
chr18:70081244 | A | G | 18 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.4374+5369T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70081244 | |||||||
chr18:70081760 | A | C | 2 | a0001c0006t0001g0125 a0002c0001t0001g0100 |
2 | HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.4374+4853T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70081760 | |||||||
chr18:70081843 | A | T | 127 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.4374+4770T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70081843 | |||||||
chr18:70082064 | G | T | 127 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.4374+4549C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082064 | |||||||
chr18:70082091 | C | A | 2 | a0002c0001t0011g0085 a0002c0019t0011g0058 |
2 | HG01981.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4374+4522G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082091 | |||||||
chr18:70082224 | A | G | 1 | a0002c0001t0001g0084 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4374+4389T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082224 | |||||||
chr18:70082422 | A | AC | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.4374+4190_4374+419 others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082422 | |||||||
chr18:70082643 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4374+3970G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082643 | |||||||
chr18:70082731 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4374+3882G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082731 | |||||||
chr18:70082800 | C | T | 1 | a0001c0006t0001g0122 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4374+3813G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70082800 | |||||||
chr18:70083090 | T | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4374+3523A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083090 | |||||||
chr18:70083117 | G | A | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.4374+3496C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083117 | |||||||
chr18:70083612 | T | C | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.4374+3001A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083612 | |||||||
chr18:70083630 | T | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4374+2983A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083630 | |||||||
chr18:70083816 | G | T | 7 | a0003c0004t0003g0008 a0003c0004t0003g0011 a0003c0004t0003g0012 others(4): Show |
7 | HG02886.hp1 HG03139.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.4374+2797C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083816 | |||||||
chr18:70083848 | C | T | 2 | a0001c0007t0001g0145 a0001c0007t0001g0146 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.4374+2765G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083848 | |||||||
chr18:70083905 | C | CT | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4374+2707dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70083905 | |||||||
chr18:70084053 | CTA | C | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.4374+2558_4374+255 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084053 | |||||||
chr18:70084115 | A | G | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.4374+2498T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084115 | |||||||
chr18:70084229 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4374+2384A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084229 | |||||||
chr18:70084230 | TA | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4374+2382delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084230 | |||||||
chr18:70084441 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4374+2172A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084441 | |||||||
chr18:70084442 | T | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4374+2171A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084442 | |||||||
chr18:70084623 | CA | C | 20 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.4374+1989delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084623 | |||||||
chr18:70084859 | A | T | 1 | a0001c0002t0002g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4374+1754T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084859 | |||||||
chr18:70084981 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4374+1632G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70084981 | |||||||
chr18:70085437 | G | A | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4374+1176C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70085437 | |||||||
chr18:70085709 | G | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4374+904C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70085709 | |||||||
chr18:70085739 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.4374+874A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70085739 | |||||||
chr18:70085742 | G | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4374+871C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70085742 | |||||||
chr18:70085925 | T | G | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4374+688A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70085925 | |||||||
chr18:70086153 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4374+460G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70086153 | |||||||
chr18:70086207 | G | C | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.4374+406C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70086207 | |||||||
chr18:70086461 | G | A | 1 | a0002c0001t0005g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4374+152C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70086461 | |||||||
chr18:70086497 | C | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4374+116G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 32/48 | chr18 | 70086497 | |||||||
chr18:70086694 | TA | T | 7 | a0001c0002t0002g0026 a0001c0002t0002g0027 a0001c0002t0002g0034 others(4): Show |
7 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-11delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAA | T | 5 | a0001c0002t0002g0028 a0001c0002t0002g0037 a0001c0002t0002g0134 others(2): Show |
5 | HG02559.hp2 HG02735.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303-12_4303-11del others(2): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(3): Show |
T | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4303-20_4303-11del others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(4): Show |
T | 6 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(3): Show |
6 | HG02300.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4303-21_4303-11del others(11): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(5): Show |
T | 18 | a0001c0010t0001g0132 a0001c0010t0004g0133 a0003c0004t0003g0006 others(15): Show |
18 | HG01081.hp2 HG01109.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4303-22_4303-11del others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(6): Show |
T | 10 | a0001c0002t0004g0108 a0001c0005t0001g0113 a0001c0007t0001g0146 others(7): Show |
10 | HG01168.hp1 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.4303-23_4303-11del others(13): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(7): Show |
T | 36 | a0001c0002t0004g0121 a0001c0002t0004g0153 a0001c0005t0002g0112 others(33): Show |
36 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.4303-24_4303-11del others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(8): Show |
T | 51 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0006t0001g0122 others(48): Show |
51 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.4303-25_4303-11del others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086694 | TAAAAAAA others(9): Show |
T | 2 | a0001c0006t0001g0001 a0002c0001t0005g0044 |
3 | HG01978.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4303-26_4303-11del others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086694 | |||||||
chr18:70086719 | AAAAAAAA others(8): Show |
A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4303-50_4303-36del others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086719 | |||||||
chr18:70086912 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4303-228G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70086912 | |||||||
chr18:70087026 | T | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4303-342A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70087026 | |||||||
chr18:70087052 | T | TAC | 10 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(7): Show |
11 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4303-370_4303-369d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70087052 | |||||||
chr18:70087364 | C | G | 1 | a0002c0003t0026g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4302+625G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70087364 | |||||||
chr18:70087440 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.4302+549C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70087440 | |||||||
chr18:70087877 | G | A | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.4302+112C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 31/48 | chr18 | 70087877 | |||||||
chr18:70088217 | T | C | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4144-70A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70088217 | |||||||
chr18:70088587 | A | G | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.4144-440T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70088587 | |||||||
chr18:70088772 | T | A | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4144-625A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70088772 | |||||||
chr18:70088920 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4144-773A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70088920 | |||||||
chr18:70089008 | T | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.4144-861A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70089008 | |||||||
chr18:70089166 | G | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4144-1019C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70089166 | |||||||
chr18:70089374 | C | G | 4 | a0001c0002t0002g0025 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4144-1227G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70089374 | |||||||
chr18:70089585 | T | C | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4144-1438A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70089585 | |||||||
chr18:70090036 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4144-1889G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090036 | |||||||
chr18:70090125 | C | G | 1 | a0002c0001t0007g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4144-1978G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090125 | |||||||
chr18:70090322 | G | A | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4143+1788C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090322 | |||||||
chr18:70090421 | GTC | G | 69 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(66): Show |
70 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.4143+1687_4143+168 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090421 | |||||||
chr18:70090456 | A | G | 5 | a0002c0003t0001g0049 a0002c0003t0001g0052 a0002c0003t0001g0055 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.4143+1654T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090456 | |||||||
chr18:70090520 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4143+1590A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090520 | |||||||
chr18:70090554 | G | C | 1 | a0002c0001t0001g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4143+1556C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090554 | |||||||
chr18:70090583 | C | T | 1 | a0002c0001t0001g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4143+1527G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090583 | |||||||
chr18:70090595 | G | C | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4143+1515C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090595 | |||||||
chr18:70090616 | T | C | 69 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(66): Show |
70 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.4143+1494A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090616 | |||||||
chr18:70090664 | C | G | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4143+1446G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090664 | |||||||
chr18:70090729 | A | G | 1 | a0001c0013t0015g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4143+1381T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090729 | |||||||
chr18:70090746 | C | T | 1 | a0001c0002t0002g0135 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4143+1364G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090746 | |||||||
chr18:70090813 | G | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.4143+1297C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090813 | |||||||
chr18:70090858 | C | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4143+1252G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090858 | |||||||
chr18:70090965 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4143+1145G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70090965 | |||||||
chr18:70091210 | A | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4143+900T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70091210 | |||||||
chr18:70091416 | T | C | 1 | a0002c0001t0005g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4143+694A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70091416 | |||||||
chr18:70091522 | G | A | 1 | a0002c0001t0005g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4143+588C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70091522 | |||||||
chr18:70091731 | A | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4143+379T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70091731 | |||||||
chr18:70091735 | A | G | 2 | a0002c0003t0001g0048 a0002c0003t0001g0154 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4143+375T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70091735 | |||||||
chr18:70092007 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4143+103G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 30/48 | chr18 | 70092007 | |||||||
chr18:70092251 | T | C | 3 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0024g0042 |
3 | HG00735.hp2 HG01978.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.4033-31A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 29/48 | chr18 | 70092251 | |||||||
chr18:70092313 | C | A | 86 | a0001c0005t0001g0141 a0001c0005t0002g0106 a0001c0005t0002g0107 others(83): Show |
87 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.4033-93G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 29/48 | chr18 | 70092313 | |||||||
chr18:70092376 | ATT | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4033-158_4033-157d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 29/48 | chr18 | 70092376 | |||||||
chr18:70092453 | G | C | 2 | a0001c0005t0002g0106 a0001c0005t0002g0107 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4032+223C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 29/48 | chr18 | 70092453 | |||||||
chr18:70092853 | A | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-49T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70092853 | |||||||
chr18:70092960 | A | G | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3904-156T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70092960 | |||||||
chr18:70093041 | T | C | 1 | a0001c0006t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3904-237A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093041 | |||||||
chr18:70093259 | TA | T | 20 | a0001c0023t0014g0155 a0003c0004t0003g0002 a0003c0004t0003g0003 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.3904-456delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093259 | |||||||
chr18:70093259 | TAA | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3904-457_3904-456d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093259 | |||||||
chr18:70093281 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3904-477A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093281 | |||||||
chr18:70093382 | T | C | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3904-578A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093382 | |||||||
chr18:70093559 | T | C | 1 | a0002c0001t0005g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3904-755A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093559 | |||||||
chr18:70093570 | T | C | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3904-766A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093570 | |||||||
chr18:70093626 | C | T | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3904-822G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093626 | |||||||
chr18:70093680 | G | C | 3 | a0002c0001t0001g0084 a0002c0001t0001g0104 a0002c0001t0002g0103 |
3 | HG01255.hp1 HG02074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3904-876C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093680 | |||||||
chr18:70093832 | G | C | 1 | a0001c0006t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3904-1028C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093832 | |||||||
chr18:70093838 | CTCTTT | C | 17 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.3904-1039_3904-103 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70093838 | |||||||
chr18:70094080 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3904-1276G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094080 | |||||||
chr18:70094098 | ACT | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3904-1296_3904-129 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094098 | |||||||
chr18:70094225 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3904-1421C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094225 | |||||||
chr18:70094250 | C | G | 1 | a0002c0020t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3904-1446G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094250 | |||||||
chr18:70094265 | T | G | 13 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(10): Show |
14 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3904-1461A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094265 | |||||||
chr18:70094730 | C | T | 3 | a0001c0013t0015g0127 a0001c0013t0016g0129 a0002c0001t0007g0059 |
3 | HG02040.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3904-1926G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094730 | |||||||
chr18:70094802 | G | A | 1 | a0002c0001t0005g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3904-1998C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094802 | |||||||
chr18:70094858 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3904-2054G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70094858 | |||||||
chr18:70095063 | G | GT | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3904-2260dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095063 | |||||||
chr18:70095063 | G | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3904-2259C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095063 | |||||||
chr18:70095115 | T | C | 1 | a0001c0007t0001g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3904-2311A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095115 | |||||||
chr18:70095127 | C | CT | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3904-2324dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095127 | |||||||
chr18:70095132 | T | TG | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3904-2329_3904-232 others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095132 | |||||||
chr18:70095175 | A | G | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3904-2371T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095175 | |||||||
chr18:70095266 | G | A | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3904-2462C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095266 | |||||||
chr18:70095342 | C | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3904-2538G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095342 | |||||||
chr18:70095424 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3904-2620A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095424 | |||||||
chr18:70095696 | G | A | 2 | a0002c0001t0001g0076 a0002c0001t0004g0093 |
2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3904-2892C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095696 | |||||||
chr18:70095788 | C | T | 15 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3904-2984G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095788 | |||||||
chr18:70095938 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3904-3134G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095938 | |||||||
chr18:70095998 | G | GT | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG01169.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3904-3195dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70095998 | |||||||
chr18:70096003 | T | A | 1 | a0003c0004t0003g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3904-3199A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096003 | |||||||
chr18:70096009 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3904-3205A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096009 | |||||||
chr18:70096165 | C | T | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3904-3361G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096165 | |||||||
chr18:70096272 | T | C | 1 | a0001c0002t0002g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3904-3468A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096272 | |||||||
chr18:70096399 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3904-3595G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096399 | |||||||
chr18:70096467 | C | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3904-3663G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096467 | |||||||
chr18:70096689 | T | C | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3904-3885A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096689 | |||||||
chr18:70096721 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3904-3917C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096721 | |||||||
chr18:70096734 | C | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3904-3930G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096734 | |||||||
chr18:70096768 | G | A | 1 | a0001c0002t0002g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3904-3964C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70096768 | |||||||
chr18:70097057 | A | G | 1 | a0002c0001t0024g0042 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3904-4253T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097057 | |||||||
chr18:70097221 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3904-4417C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097221 | |||||||
chr18:70097508 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-4704C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097508 | |||||||
chr18:70097513 | G | A | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3904-4709C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097513 | |||||||
chr18:70097571 | G | A | 4 | a0001c0002t0002g0026 a0001c0002t0002g0029 a0001c0002t0002g0041 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3904-4767C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097571 | |||||||
chr18:70097594 | C | T | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3904-4790G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097594 | |||||||
chr18:70097595 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-4791C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097595 | |||||||
chr18:70097619 | G | C | 14 | a0002c0003t0001g0048 a0002c0003t0001g0050 a0002c0003t0001g0053 others(11): Show |
14 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.3904-4815C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097619 | |||||||
chr18:70097865 | C | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3904-5061G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70097865 | |||||||
chr18:70098061 | ATAAAC | A | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.3904-5262_3904-525 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098061 | |||||||
chr18:70098246 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-5442G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098246 | |||||||
chr18:70098557 | T | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3904-5753A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098557 | |||||||
chr18:70098609 | C | A | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3904-5805G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098609 | |||||||
chr18:70098796 | C | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3904-5992G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098796 | |||||||
chr18:70098916 | G | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3904-6112C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098916 | |||||||
chr18:70098928 | C | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3904-6124G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70098928 | |||||||
chr18:70099073 | T | C | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3904-6269A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099073 | |||||||
chr18:70099293 | T | A | 1 | a0002c0001t0009g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3904-6489A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099293 | |||||||
chr18:70099330 | T | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3904-6526A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099330 | |||||||
chr18:70099398 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3904-6594G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099398 | |||||||
chr18:70099409 | C | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3904-6605G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099409 | |||||||
chr18:70099426 | A | G | 1 | a0002c0001t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3904-6622T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099426 | |||||||
chr18:70099464 | T | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3904-6660A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099464 | |||||||
chr18:70099612 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3904-6808A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099612 | |||||||
chr18:70099757 | G | A | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.3904-6953C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70099757 | |||||||
chr18:70100013 | G | A | 100 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(97): Show |
101 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.3904-7209C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100013 | |||||||
chr18:70100043 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-7239C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100043 | |||||||
chr18:70100192 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3904-7388A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100192 | |||||||
chr18:70100403 | T | C | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3904-7599A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100403 | |||||||
chr18:70100531 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3904-7727G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100531 | |||||||
chr18:70100713 | C | T | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.3904-7909G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100713 | |||||||
chr18:70100807 | T | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3904-8003A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100807 | |||||||
chr18:70100948 | G | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3904-8144C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100948 | |||||||
chr18:70100955 | C | T | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3904-8151G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100955 | |||||||
chr18:70100976 | T | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3904-8172A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70100976 | |||||||
chr18:70101005 | T | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3904-8201A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101005 | |||||||
chr18:70101012 | C | T | 2 | a0003c0004t0006g0014 a0003c0004t0006g0017 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3904-8208G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101012 | |||||||
chr18:70101262 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+8236A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101262 | |||||||
chr18:70101303 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3903+8195G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101303 | |||||||
chr18:70101585 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+7913C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101585 | |||||||
chr18:70101590 | G | A | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3903+7908C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101590 | |||||||
chr18:70101593 | C | A | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3903+7905G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101593 | |||||||
chr18:70101678 | A | G | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3903+7820T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101678 | |||||||
chr18:70101831 | C | T | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.3903+7667G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101831 | |||||||
chr18:70101914 | C | G | 1 | a0001c0007t0001g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3903+7584G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101914 | |||||||
chr18:70101955 | C | A | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3903+7543G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70101955 | |||||||
chr18:70102032 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3903+7466C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102032 | |||||||
chr18:70102265 | C | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3903+7233G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102265 | |||||||
chr18:70102334 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3903+7164G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102334 | |||||||
chr18:70102377 | G | A | 1 | a0001c0006t0020g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3903+7121C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102377 | |||||||
chr18:70102425 | T | C | 1 | a0002c0003t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3903+7073A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102425 | |||||||
chr18:70102477 | G | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+7021C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102477 | |||||||
chr18:70102746 | A | G | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3903+6752T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102746 | |||||||
chr18:70102767 | A | G | 141 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.3903+6731T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102767 | |||||||
chr18:70102897 | TGCCCCGT others(30): Show |
T | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3903+6564_3903+660 others(41): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70102897 | |||||||
chr18:70103009 | G | A | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.3903+6489C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103009 | |||||||
chr18:70103014 | G | A | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3903+6484C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103014 | |||||||
chr18:70103032 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+6466C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103032 | |||||||
chr18:70103087 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3903+6411G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103087 | |||||||
chr18:70103106 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+6392C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103106 | |||||||
chr18:70103163 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3903+6335A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103163 | |||||||
chr18:70103218 | G | C | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3903+6280C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103218 | |||||||
chr18:70103244 | C | T | 1 | a0001c0007t0001g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3903+6254G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103244 | |||||||
chr18:70103267 | G | A | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3903+6231C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103267 | |||||||
chr18:70103274 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3903+6224C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103274 | |||||||
chr18:70103279 | C | T | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3903+6219G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103279 | |||||||
chr18:70103466 | C | G | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3903+6032G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103466 | |||||||
chr18:70103568 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3903+5930G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103568 | |||||||
chr18:70103618 | G | A | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3903+5880C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103618 | |||||||
chr18:70103619 | C | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3903+5879G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103619 | |||||||
chr18:70103620 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3903+5878C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103620 | |||||||
chr18:70103670 | T | G | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3903+5828A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103670 | |||||||
chr18:70103762 | C | CA | 148 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(146): Show |
intron_variant | MODIFIER | c.3903+5735dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103762 | |||||||
chr18:70103951 | C | T | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.3903+5547G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70103951 | |||||||
chr18:70104107 | C | T | 9 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3903+5391G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104107 | |||||||
chr18:70104161 | G | A | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3903+5337C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104161 | |||||||
chr18:70104174 | G | A | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3903+5324C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104174 | |||||||
chr18:70104479 | A | G | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3903+5019T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104479 | |||||||
chr18:70104494 | A | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3903+5004T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104494 | |||||||
chr18:70104593 | C | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3903+4905G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104593 | |||||||
chr18:70104700 | A | T | 1 | a0001c0006t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3903+4798T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104700 | |||||||
chr18:70104724 | C | T | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3903+4774G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104724 | |||||||
chr18:70104867 | CA | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3903+4630delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104867 | |||||||
chr18:70104885 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+4613C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104885 | |||||||
chr18:70104923 | C | T | 1 | a0003c0004t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3903+4575G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70104923 | |||||||
chr18:70105001 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3903+4497C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105001 | |||||||
chr18:70105026 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+4472C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105026 | |||||||
chr18:70105039 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3903+4459C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105039 | |||||||
chr18:70105174 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+4324A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105174 | |||||||
chr18:70105281 | G | A | 14 | a0002c0003t0001g0048 a0002c0003t0001g0050 a0002c0003t0001g0053 others(11): Show |
14 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.3903+4217C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105281 | |||||||
chr18:70105302 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3903+4196C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105302 | |||||||
chr18:70105456 | G | A | 4 | a0001c0002t0002g0025 a0001c0002t0002g0135 a0001c0002t0002g0136 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3903+4042C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105456 | |||||||
chr18:70105485 | C | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3903+4013G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105485 | |||||||
chr18:70105561 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+3937C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105561 | |||||||
chr18:70105625 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3903+3873G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70105625 | |||||||
chr18:70106072 | T | G | 128 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.3903+3426A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106072 | |||||||
chr18:70106134 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3903+3364C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106134 | |||||||
chr18:70106376 | TG | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+3121delC | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106376 | |||||||
chr18:70106378 | T | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+3120A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106378 | |||||||
chr18:70106381 | T | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+3117A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106381 | |||||||
chr18:70106382 | A | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+3116T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106382 | |||||||
chr18:70106559 | A | G | 1 | a0001c0002t0002g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3903+2939T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106559 | |||||||
chr18:70106652 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+2846A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106652 | |||||||
chr18:70106738 | A | G | 106 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(103): Show |
107 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.3903+2760T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106738 | |||||||
chr18:70106990 | T | C | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3903+2508A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70106990 | |||||||
chr18:70107013 | A | C | 10 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0051 others(7): Show |
10 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.3903+2485T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70107013 | |||||||
chr18:70107137 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3903+2361G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70107137 | |||||||
chr18:70107153 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+2345C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70107153 | |||||||
chr18:70107475 | C | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+2023G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70107475 | |||||||
chr18:70107782 | A | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3903+1716T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70107782 | |||||||
chr18:70108015 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3903+1483G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108015 | |||||||
chr18:70108017 | G | A | 15 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3903+1481C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108017 | |||||||
chr18:70108120 | G | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3903+1378C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108120 | |||||||
chr18:70108137 | C | T | 1 | a0002c0001t0013g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3903+1361G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108137 | |||||||
chr18:70108149 | C | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3903+1349G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108149 | |||||||
chr18:70108276 | C | CA | 7 | a0001c0002t0002g0027 a0001c0002t0002g0034 a0001c0005t0002g0106 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3903+1221dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108276 | |||||||
chr18:70108276 | CA | C | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.3903+1221delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108276 | |||||||
chr18:70108452 | A | G | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3903+1046T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108452 | |||||||
chr18:70108644 | C | T | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.3903+854G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108644 | |||||||
chr18:70108865 | C | CA | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3903+632dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70108865 | |||||||
chr18:70109156 | G | A | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3903+342C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70109156 | |||||||
chr18:70109175 | G | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3903+323C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70109175 | |||||||
chr18:70109211 | G | A | 2 | a0003c0004t0006g0014 a0003c0004t0006g0017 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3903+287C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70109211 | |||||||
chr18:70109236 | C | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3903+262G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70109236 | |||||||
chr18:70109278 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3903+220T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 28/48 | chr18 | 70109278 | |||||||
chr18:70109826 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3684-109A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70109826 | |||||||
chr18:70109838 | A | T | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3684-121T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70109838 | |||||||
chr18:70109927 | G | A | 1 | a0001c0006t0021g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3684-210C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70109927 | |||||||
chr18:70110109 | T | C | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.3684-392A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110109 | |||||||
chr18:70110236 | TA | T | 7 | a0001c0002t0002g0027 a0001c0005t0002g0106 a0001c0006t0001g0123 others(4): Show |
7 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.3684-520delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110236 | |||||||
chr18:70110237 | A | T | 3 | a0001c0010t0001g0132 a0001c0010t0004g0133 a0006c0014t0022g0046 |
3 | HG02280.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3684-520T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110237 | |||||||
chr18:70110534 | C | T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3684-817G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110534 | |||||||
chr18:70110649 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3684-932G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110649 | |||||||
chr18:70110795 | A | G | 1 | a0002c0003t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3684-1078T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110795 | |||||||
chr18:70110877 | G | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3684-1160C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70110877 | |||||||
chr18:70111052 | A | G | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3684-1335T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111052 | |||||||
chr18:70111196 | C | T | 1 | a0001c0006t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3684-1479G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111196 | |||||||
chr18:70111282 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3684-1565C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111282 | |||||||
chr18:70111348 | G | C | 6 | a0002c0001t0001g0073 a0002c0001t0001g0095 a0002c0001t0004g0077 others(3): Show |
6 | HG01169.hp2 HG01243.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.3684-1631C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111348 | |||||||
chr18:70111392 | C | G | 29 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(26): Show |
29 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.3684-1675G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111392 | |||||||
chr18:70111414 | A | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3684-1697T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111414 | |||||||
chr18:70111522 | T | C | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3684-1805A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111522 | |||||||
chr18:70111558 | T | C | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3684-1841A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111558 | |||||||
chr18:70111609 | G | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3684-1892C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111609 | |||||||
chr18:70111680 | G | A | 1 | a0001c0002t0004g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3684-1963C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111680 | |||||||
chr18:70111734 | G | A | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3684-2017C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111734 | |||||||
chr18:70111762 | T | C | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3684-2045A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70111762 | |||||||
chr18:70112046 | A | T | 1 | a0003c0004t0003g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3684-2329T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112046 | |||||||
chr18:70112325 | C | T | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3683+2120G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112325 | |||||||
chr18:70112483 | C | CA | 6 | a0001c0002t0001g0035 a0001c0002t0002g0030 a0001c0002t0002g0031 others(3): Show |
6 | HG02300.hp2 HG02809.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3683+1961dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112483 | |||||||
chr18:70112483 | C | CAA | 13 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(10): Show |
14 | HG00099.hp2 HG00639.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.3683+1960_3683+196 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112483 | |||||||
chr18:70112483 | C | CAAA | 63 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(60): Show |
63 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3683+1959_3683+196 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112483 | |||||||
chr18:70112483 | C | CAAAA | 25 | a0001c0005t0001g0141 a0001c0007t0001g0150 a0001c0013t0015g0127 others(22): Show |
25 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.3683+1958_3683+196 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112483 | |||||||
chr18:70112543 | A | T | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3683+1902T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112543 | |||||||
chr18:70112947 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3683+1498G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70112947 | |||||||
chr18:70113093 | G | A | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3683+1352C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113093 | |||||||
chr18:70113237 | CA | C | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3683+1207delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113237 | |||||||
chr18:70113263 | G | A | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3683+1182C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113263 | |||||||
chr18:70113320 | T | C | 5 | a0002c0003t0001g0049 a0002c0003t0001g0052 a0002c0003t0001g0055 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3683+1125A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113320 | |||||||
chr18:70113586 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3683+859G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113586 | |||||||
chr18:70113608 | A | G | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3683+837T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113608 | |||||||
chr18:70113665 | T | G | 1 | a0001c0007t0001g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3683+780A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113665 | |||||||
chr18:70113673 | C | T | 4 | a0002c0003t0001g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3683+772G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113673 | |||||||
chr18:70113720 | A | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3683+725T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113720 | |||||||
chr18:70113785 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3683+660G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113785 | |||||||
chr18:70113792 | G | A | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3683+653C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113792 | |||||||
chr18:70113975 | T | C | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3683+470A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 27/48 | chr18 | 70113975 | |||||||
chr18:70115219 | T | C | 1 | a0002c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3529-620A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115219 | |||||||
chr18:70115227 | T | C | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3529-628A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115227 | |||||||
chr18:70115417 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3529-818A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115417 | |||||||
chr18:70115520 | T | TA | 85 | a0001c0005t0001g0111 a0001c0005t0001g0141 a0001c0006t0001g0001 others(82): Show |
86 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3529-922dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115520 | |||||||
chr18:70115520 | T | TAA | 12 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(9): Show |
12 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3529-923_3529-922d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115520 | |||||||
chr18:70115607 | T | C | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3529-1008A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115607 | |||||||
chr18:70115628 | T | C | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3529-1029A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115628 | |||||||
chr18:70115631 | T | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3529-1032A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115631 | |||||||
chr18:70115729 | T | C | 1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3529-1130A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115729 | |||||||
chr18:70115736 | A | T | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3529-1137T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115736 | |||||||
chr18:70115765 | A | T | 2 | a0001c0002t0002g0027 a0001c0002t0002g0034 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3529-1166T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115765 | |||||||
chr18:70115797 | A | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3529-1198T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115797 | |||||||
chr18:70115826 | C | T | 1 | a0003c0004t0003g0019 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3529-1227G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70115826 | |||||||
chr18:70116454 | T | G | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3529-1855A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70116454 | |||||||
chr18:70116916 | C | CA | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3529-2318dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70116916 | |||||||
chr18:70117014 | ACTC | A | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.3529-2418_3529-241 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117014 | |||||||
chr18:70117387 | T | C | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3529-2788A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117387 | |||||||
chr18:70117514 | T | C | 1 | a0003c0004t0006g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3529-2915A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117514 | |||||||
chr18:70117537 | C | T | 3 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 |
3 | HG02970.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3529-2938G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117537 | |||||||
chr18:70117538 | G | A | 1 | a0004c0025t0001g0144 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3529-2939C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117538 | |||||||
chr18:70117611 | A | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3529-3012T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117611 | |||||||
chr18:70117784 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3529-3185G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117784 | |||||||
chr18:70117918 | T | A | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.3529-3319A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117918 | |||||||
chr18:70117931 | G | C | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3529-3332C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117931 | |||||||
chr18:70117960 | A | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3529-3361T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70117960 | |||||||
chr18:70118036 | T | C | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3529-3437A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118036 | |||||||
chr18:70118075 | T | C | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.3529-3476A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118075 | |||||||
chr18:70118447 | A | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3528+3109T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118447 | |||||||
chr18:70118452 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3528+3104G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118452 | |||||||
chr18:70118459 | C | CA | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3528+3096dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118459 | |||||||
chr18:70118506 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3528+3050G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118506 | |||||||
chr18:70118587 | C | T | 25 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(22): Show |
26 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.3528+2969G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118587 | |||||||
chr18:70118672 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3528+2884T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118672 | |||||||
chr18:70118760 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3528+2796C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118760 | |||||||
chr18:70118793 | G | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3528+2763C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118793 | |||||||
chr18:70118961 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3528+2595G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118961 | |||||||
chr18:70118982 | A | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3528+2574T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70118982 | |||||||
chr18:70119251 | T | A | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.3528+2305A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119251 | |||||||
chr18:70119324 | C | CA | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3528+2231dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119324 | |||||||
chr18:70119669 | G | A | 2 | a0002c0001t0005g0043 a0002c0001t0024g0042 |
2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3528+1887C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119669 | |||||||
chr18:70119669 | G | T | 1 | a0002c0001t0001g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3528+1887C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119669 | |||||||
chr18:70119854 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3528+1702A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119854 | |||||||
chr18:70119901 | G | A | 2 | a0002c0001t0011g0085 a0002c0019t0011g0058 |
2 | HG01981.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3528+1655C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119901 | |||||||
chr18:70119982 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3528+1574G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70119982 | |||||||
chr18:70120117 | A | G | 13 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(10): Show |
14 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3528+1439T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120117 | |||||||
chr18:70120225 | CAG | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3528+1329_3528+133 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120225 | |||||||
chr18:70120450 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3528+1106T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120450 | |||||||
chr18:70120704 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3528+852G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120704 | |||||||
chr18:70120854 | G | A | 1 | a0002c0001t0005g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3528+702C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120854 | |||||||
chr18:70120916 | T | G | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3528+640A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120916 | |||||||
chr18:70120932 | T | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3528+624A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120932 | |||||||
chr18:70120999 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3528+557G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70120999 | |||||||
chr18:70121005 | C | T | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3528+551G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121005 | |||||||
chr18:70121059 | T | TA | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3528+496dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121059 | |||||||
chr18:70121105 | G | A | 12 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(9): Show |
13 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.3528+451C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121105 | |||||||
chr18:70121159 | A | G | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.3528+397T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121159 | |||||||
chr18:70121179 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3528+377G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121179 | |||||||
chr18:70121192 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3528+364G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121192 | |||||||
chr18:70121354 | C | T | 3 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0024g0042 |
3 | HG00735.hp2 HG01978.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3528+202G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121354 | |||||||
chr18:70121363 | T | C | 7 | a0002c0001t0005g0051 a0002c0001t0007g0059 a0002c0001t0007g0060 others(4): Show |
7 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.3528+193A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121363 | |||||||
chr18:70121520 | C | T | 1 | a0002c0001t0005g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3528+36G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 26/48 | chr18 | 70121520 | |||||||
chr18:70121724 | T | C | 1 | a0002c0001t0005g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3384-24A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70121724 | |||||||
chr18:70121926 | G | C | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3384-226C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70121926 | |||||||
chr18:70122003 | C | G | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.3384-303G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122003 | |||||||
chr18:70122108 | T | A | 4 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG03225.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3384-408A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122108 | |||||||
chr18:70122200 | G | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.3384-500C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122200 | |||||||
chr18:70122349 | T | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3384-649A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122349 | |||||||
chr18:70122449 | A | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3384-749T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122449 | |||||||
chr18:70122480 | G | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3384-780C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122480 | |||||||
chr18:70122866 | T | C | 9 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0074 others(6): Show |
9 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3384-1166A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122866 | |||||||
chr18:70122945 | C | G | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3384-1245G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70122945 | |||||||
chr18:70123073 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3384-1373A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70123073 | |||||||
chr18:70123150 | A | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3384-1450T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70123150 | |||||||
chr18:70123273 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3384-1573A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70123273 | |||||||
chr18:70123333 | CTCTGTGG others(15): Show |
C | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3384-1655_3384-163 others(26): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70123333 | |||||||
chr18:70123460 | A | G | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3384-1760T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70123460 | |||||||
chr18:70124118 | G | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3384-2418C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124118 | |||||||
chr18:70124158 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3384-2458C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124158 | |||||||
chr18:70124241 | T | G | 94 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.3384-2541A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124241 | |||||||
chr18:70124463 | T | A | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3384-2763A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124463 | |||||||
chr18:70124510 | A | T | 89 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(86): Show |
90 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.3384-2810T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124510 | |||||||
chr18:70124653 | T | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3383+2849A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124653 | |||||||
chr18:70124753 | C | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3383+2749G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124753 | |||||||
chr18:70124757 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3383+2745C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70124757 | |||||||
chr18:70125251 | G | A | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3383+2251C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70125251 | |||||||
chr18:70125429 | T | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3383+2073A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70125429 | |||||||
chr18:70125853 | G | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.3383+1649C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70125853 | |||||||
chr18:70125894 | G | C | 1 | a0003c0004t0006g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3383+1608C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70125894 | |||||||
chr18:70126075 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3383+1427A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126075 | |||||||
chr18:70126218 | T | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3383+1284A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126218 | |||||||
chr18:70126333 | T | TA | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3383+1168dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126333 | |||||||
chr18:70126366 | G | A | 1 | a0003c0004t0006g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3383+1136C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126366 | |||||||
chr18:70126413 | T | C | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3383+1089A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126413 | |||||||
chr18:70126683 | T | C | 2 | a0001c0002t0002g0031 a0001c0002t0002g0033 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3383+819A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126683 | |||||||
chr18:70126724 | G | T | 10 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3383+778C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126724 | |||||||
chr18:70126856 | C | A | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3383+646G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126856 | |||||||
chr18:70126997 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3383+505C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 25/48 | chr18 | 70126997 | |||||||
chr18:70127918 | T | C | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3144-177A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/48 | chr18 | 70127918 | |||||||
chr18:70128015 | C | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.3144-274G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/48 | chr18 | 70128015 | |||||||
chr18:70128147 | C | T | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3143+211G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/48 | chr18 | 70128147 | |||||||
chr18:70128214 | G | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3143+144C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/48 | chr18 | 70128214 | |||||||
chr18:70128314 | A | G | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3143+44T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 24/48 | chr18 | 70128314 | |||||||
chr18:70129285 | A | C | 1 | a0002c0003t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2955-739T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129285 | |||||||
chr18:70129442 | C | G | 1 | a0002c0020t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2955-896G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129442 | |||||||
chr18:70129498 | C | G | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955-952G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129498 | |||||||
chr18:70129644 | T | TA | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.2955-1099dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129644 | |||||||
chr18:70129931 | AAAT | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2955-1388_2955-138 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129931 | |||||||
chr18:70129937 | T | C | 7 | a0001c0002t0001g0139 a0001c0002t0002g0025 a0001c0002t0002g0134 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955-1391A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70129937 | |||||||
chr18:70130084 | C | T | 3 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0024g0042 |
3 | HG00735.hp2 HG01978.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2955-1538G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70130084 | |||||||
chr18:70130288 | A | T | 1 | a0001c0006t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2955-1742T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70130288 | |||||||
chr18:70130409 | A | T | 54 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(51): Show |
54 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2955-1863T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70130409 | |||||||
chr18:70130701 | G | C | 2 | a0001c0009t0001g0039 a0001c0009t0001g0040 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2955-2155C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70130701 | |||||||
chr18:70131017 | C | T | 96 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.2955-2471G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131017 | |||||||
chr18:70131146 | TA | T | 125 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.2955-2601delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131146 | |||||||
chr18:70131183 | A | G | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2955-2637T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131183 | |||||||
chr18:70131357 | A | C | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2955-2811T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131357 | |||||||
chr18:70131432 | C | T | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2955-2886G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131432 | |||||||
chr18:70131583 | G | A | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2954+2890C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131583 | |||||||
chr18:70131809 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2954+2664G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131809 | |||||||
chr18:70131809 | C | T | 18 | a0001c0002t0001g0035 a0001c0002t0002g0026 a0001c0002t0002g0027 others(15): Show |
18 | HG01346.hp2 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2954+2664G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70131809 | |||||||
chr18:70132002 | T | C | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2954+2471A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132002 | |||||||
chr18:70132280 | C | G | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2954+2193G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132280 | |||||||
chr18:70132286 | A | G | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2954+2187T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132286 | |||||||
chr18:70132296 | T | C | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2954+2177A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132296 | |||||||
chr18:70132472 | AAATATT | A | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.2954+1995_2954+200 others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132472 | |||||||
chr18:70132499 | A | G | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2954+1974T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132499 | |||||||
chr18:70132509 | C | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2954+1964G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132509 | |||||||
chr18:70132559 | T | TA | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2954+1913dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132559 | |||||||
chr18:70132684 | C | A | 1 | a0002c0003t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2954+1789G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132684 | |||||||
chr18:70132901 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2954+1572G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70132901 | |||||||
chr18:70133133 | G | A | 2 | a0001c0005t0002g0106 a0001c0005t0002g0107 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2954+1340C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133133 | |||||||
chr18:70133219 | A | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2954+1254T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133219 | |||||||
chr18:70133617 | G | GC | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.2954+855dupG | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133617 | |||||||
chr18:70133792 | C | T | 1 | a0002c0020t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2954+681G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133792 | |||||||
chr18:70133847 | C | T | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2954+626G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133847 | |||||||
chr18:70133991 | C | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2954+482G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70133991 | |||||||
chr18:70134133 | T | C | 95 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(92): Show |
96 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.2954+340A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70134133 | |||||||
chr18:70134134 | G | A | 1 | a0001c0008t0008g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2954+339C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70134134 | |||||||
chr18:70134183 | A | G | 1 | a0001c0005t0002g0106 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2954+290T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70134183 | |||||||
chr18:70134240 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2954+233A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70134240 | |||||||
chr18:70134323 | A | G | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2954+150T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 23/48 | chr18 | 70134323 | |||||||
chr18:70134725 | G | A | 3 | a0002c0001t0001g0072 a0002c0001t0001g0078 a0005c0015t0001g0069 |
3 | HG01257.hp1 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2886-184C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/48 | chr18 | 70134725 | |||||||
chr18:70134788 | G | A | 1 | a0002c0003t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2886-247C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/48 | chr18 | 70134788 | |||||||
chr18:70134840 | T | C | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2886-299A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/48 | chr18 | 70134840 | |||||||
chr18:70134938 | CA | C | 6 | a0001c0002t0002g0025 a0001c0002t0002g0134 a0001c0002t0002g0135 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2885+245delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/48 | chr18 | 70134938 | |||||||
chr18:70135014 | T | C | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.2885+170A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 22/48 | chr18 | 70135014 | |||||||
chr18:70135759 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2789-479A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70135759 | |||||||
chr18:70135946 | A | G | 10 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(7): Show |
10 | HG00099.hp2 HG00639.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2789-666T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70135946 | |||||||
chr18:70136003 | T | C | 1 | a0001c0007t0001g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2789-723A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136003 | |||||||
chr18:70136138 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2789-858G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136138 | |||||||
chr18:70136225 | G | GA | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.2789-946dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136225 | |||||||
chr18:70136280 | G | A | 89 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(86): Show |
90 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.2789-1000C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136280 | |||||||
chr18:70136337 | T | C | 1 | a0002c0003t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2789-1057A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136337 | |||||||
chr18:70136414 | T | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2789-1134A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136414 | |||||||
chr18:70136425 | ATAAATT | A | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2789-1151_2789-114 others(10): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136425 | |||||||
chr18:70136634 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2789-1354A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136634 | |||||||
chr18:70136650 | A | C | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2789-1370T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136650 | |||||||
chr18:70136725 | G | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2789-1445C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136725 | |||||||
chr18:70136788 | CCAACACT others(5): Show |
C | 10 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(7): Show |
10 | HG00099.hp2 HG00639.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2789-1520_2789-150 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136788 | |||||||
chr18:70136867 | T | C | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2789-1587A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136867 | |||||||
chr18:70136868 | A | C | 7 | a0002c0003t0001g0047 a0002c0003t0001g0048 a0002c0003t0001g0050 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2789-1588T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136868 | |||||||
chr18:70136949 | A | T | 1 | a0001c0006t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2789-1669T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70136949 | |||||||
chr18:70137033 | G | GA | 5 | a0001c0002t0001g0035 a0001c0002t0002g0030 a0001c0002t0002g0031 others(2): Show |
5 | HG02809.hp1 HG03225.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2789-1754dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137033 | |||||||
chr18:70137057 | T | G | 18 | a0001c0002t0001g0035 a0001c0002t0002g0026 a0001c0002t0002g0027 others(15): Show |
18 | HG01346.hp2 HG01884.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2789-1777A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137057 | |||||||
chr18:70137058 | T | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2789-1778A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137058 | |||||||
chr18:70137073 | G | A | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2789-1793C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137073 | |||||||
chr18:70137220 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2789-1940C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137220 | |||||||
chr18:70137259 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2789-1979A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137259 | |||||||
chr18:70137388 | A | G | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.2789-2108T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137388 | |||||||
chr18:70137532 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2788+2067G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137532 | |||||||
chr18:70137545 | G | C | 1 | a0002c0003t0026g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2788+2054C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137545 | |||||||
chr18:70137773 | C | T | 1 | a0002c0001t0001g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2788+1826G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137773 | |||||||
chr18:70137836 | A | G | 1 | a0002c0001t0005g0051 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2788+1763T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137836 | |||||||
chr18:70137941 | C | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2788+1658G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70137941 | |||||||
chr18:70138033 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2788+1566G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70138033 | |||||||
chr18:70138035 | T | C | 25 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(22): Show |
26 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2788+1564A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70138035 | |||||||
chr18:70138091 | C | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2788+1508G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70138091 | |||||||
chr18:70138507 | A | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2788+1092T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70138507 | |||||||
chr18:70138653 | C | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2788+946G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70138653 | |||||||
chr18:70139000 | G | GA | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2788+598dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70139000 | |||||||
chr18:70139055 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2788+544A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70139055 | |||||||
chr18:70139281 | A | G | 29 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(26): Show |
29 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.2788+318T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 21/48 | chr18 | 70139281 | |||||||
chr18:70140032 | A | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2670+68T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 20/48 | chr18 | 70140032 | |||||||
chr18:70140465 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2582-277G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140465 | |||||||
chr18:70140479 | T | C | 1 | a0002c0003t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2582-291A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140479 | |||||||
chr18:70140523 | T | C | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2582-335A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140523 | |||||||
chr18:70140620 | C | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582-432G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140620 | |||||||
chr18:70140636 | C | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2582-448G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140636 | |||||||
chr18:70140689 | CTATA | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2582-505_2582-502d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140689 | |||||||
chr18:70140809 | C | T | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2582-621G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140809 | |||||||
chr18:70140825 | A | T | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2582-637T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140825 | |||||||
chr18:70140828 | G | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2582-640C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140828 | |||||||
chr18:70140957 | T | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2582-769A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140957 | |||||||
chr18:70140975 | G | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2582-787C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70140975 | |||||||
chr18:70141168 | A | T | 1 | a0001c0002t0002g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2582-980T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141168 | |||||||
chr18:70141197 | T | A | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2582-1009A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141197 | |||||||
chr18:70141198 | C | A | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2582-1010G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141198 | |||||||
chr18:70141266 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2581+1022G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141266 | |||||||
chr18:70141604 | C | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2581+684G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141604 | |||||||
chr18:70141613 | G | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2581+675C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141613 | |||||||
chr18:70141859 | A | G | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.2581+429T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141859 | |||||||
chr18:70141936 | C | G | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2581+352G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 19/48 | chr18 | 70141936 | |||||||
chr18:70142411 | A | C | 96 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.2482-24T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70142411 | |||||||
chr18:70142412 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-25G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70142412 | |||||||
chr18:70142625 | A | G | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2482-238T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70142625 | |||||||
chr18:70143056 | C | A | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2482-669G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143056 | |||||||
chr18:70143073 | C | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2482-686G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143073 | |||||||
chr18:70143323 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2482-936G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143323 | |||||||
chr18:70143332 | C | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2482-945G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143332 | |||||||
chr18:70143462 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2482-1075C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143462 | |||||||
chr18:70143525 | T | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-1138A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143525 | |||||||
chr18:70143576 | C | T | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2482-1189G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143576 | |||||||
chr18:70143640 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2482-1253G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143640 | |||||||
chr18:70143641 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2482-1254C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143641 | |||||||
chr18:70143662 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2482-1275C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143662 | |||||||
chr18:70143920 | T | C | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2482-1533A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70143920 | |||||||
chr18:70144186 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2481+1426T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70144186 | |||||||
chr18:70145087 | G | A | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.2481+525C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145087 | |||||||
chr18:70145167 | A | G | 1 | a0001c0006t0020g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2481+445T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145167 | |||||||
chr18:70145212 | C | T | 23 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(20): Show |
23 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.2481+400G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145212 | |||||||
chr18:70145226 | A | G | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.2481+386T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145226 | |||||||
chr18:70145445 | G | GT | 2 | a0001c0013t0015g0127 a0001c0013t0016g0129 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2481+166dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145445 | |||||||
chr18:70145537 | G | A | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2481+75C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 18/48 | chr18 | 70145537 | |||||||
chr18:70145836 | TTA | T | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310-55_2310-54del others(2): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70145836 | |||||||
chr18:70146009 | T | C | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310-226A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146009 | |||||||
chr18:70146074 | C | T | 1 | a0001c0002t0002g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2310-291G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146074 | |||||||
chr18:70146119 | T | G | 2 | a0001c0009t0001g0039 a0001c0009t0001g0040 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2310-336A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146119 | |||||||
chr18:70146121 | C | A | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2310-338G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146121 | |||||||
chr18:70146577 | G | A | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2310-794C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146577 | |||||||
chr18:70146624 | G | T | 60 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(57): Show |
60 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2310-841C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146624 | |||||||
chr18:70146625 | C | T | 1 | a0001c0002t0002g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2310-842G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146625 | |||||||
chr18:70146647 | T | C | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2310-864A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146647 | |||||||
chr18:70146924 | C | T | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310-1141G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70146924 | |||||||
chr18:70147138 | T | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2310-1355A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147138 | |||||||
chr18:70147261 | T | C | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2310-1478A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147261 | |||||||
chr18:70147381 | AGCAATAG | A | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2309+1513_2309+151 others(11): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147381 | |||||||
chr18:70147422 | T | C | 1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2309+1479A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147422 | |||||||
chr18:70147453 | A | T | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2309+1448T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147453 | |||||||
chr18:70147559 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2309+1342C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147559 | |||||||
chr18:70147681 | T | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2309+1220A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147681 | |||||||
chr18:70147880 | C | T | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2309+1021G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147880 | |||||||
chr18:70147951 | A | G | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.2309+950T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147951 | |||||||
chr18:70147953 | G | A | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.2309+948C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147953 | |||||||
chr18:70147961 | C | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2309+940G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70147961 | |||||||
chr18:70148009 | T | C | 8 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(5): Show |
9 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2309+892A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148009 | |||||||
chr18:70148121 | G | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2309+780C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148121 | |||||||
chr18:70148122 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2309+779G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148122 | |||||||
chr18:70148240 | C | T | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2309+661G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148240 | |||||||
chr18:70148414 | T | C | 133 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.2309+487A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148414 | |||||||
chr18:70148530 | T | G | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+371A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148530 | |||||||
chr18:70148547 | C | T | 1 | a0001c0002t0002g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2309+354G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148547 | |||||||
chr18:70148651 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.2309+250C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148651 | |||||||
chr18:70148711 | G | A | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2309+190C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148711 | |||||||
chr18:70148764 | G | A | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2309+137C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 17/48 | chr18 | 70148764 | |||||||
chr18:70149326 | G | A | 4 | a0002c0003t0001g0050 a0002c0003t0001g0053 a0002c0003t0001g0054 others(1): Show |
4 | HG02109.hp1 HG03239.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2173-289C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 16/48 | chr18 | 70149326 | |||||||
chr18:70149453 | G | C | 2 | a0001c0002t0004g0108 a0001c0002t0004g0121 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2173-416C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 16/48 | chr18 | 70149453 | |||||||
chr18:70149540 | T | TA | 88 | a0001c0002t0004g0108 a0001c0005t0001g0109 a0001c0005t0001g0110 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.2172+430_2172+431i others(3): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 16/48 | chr18 | 70149540 | |||||||
chr18:70149540 | T | TAA | 2 | a0002c0001t0005g0074 a0002c0001t0007g0059 |
2 | HG02040.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2172+430_2172+431i others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 16/48 | chr18 | 70149540 | |||||||
chr18:70149541 | T | A | 102 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(99): Show |
103 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.2172+430A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 16/48 | chr18 | 70149541 | |||||||
chr18:70150508 | T | C | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.2055+100A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 15/48 | chr18 | 70150508 | |||||||
chr18:70150575 | C | G | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2055+33G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 15/48 | chr18 | 70150575 | |||||||
chr18:70150601 | G | A | 3 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0024g0042 |
3 | HG00735.hp2 HG01978.hp2 HG02055.hp2 |
splice_region_variant&intron_variant | LOW | c.2055+7C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 15/48 | chr18 | 70150601 | |||||||
chr18:70150830 | T | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1930-97A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70150830 | |||||||
chr18:70150880 | CCTGT | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1930-151_1930-148d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70150880 | |||||||
chr18:70151006 | T | C | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-273A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70151006 | |||||||
chr18:70151902 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-1169G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70151902 | |||||||
chr18:70152142 | T | C | 1 | a0002c0001t0001g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1930-1409A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152142 | |||||||
chr18:70152174 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1930-1441C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152174 | |||||||
chr18:70152204 | A | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-1471T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152204 | |||||||
chr18:70152215 | GCTGATGA others(1): Show |
G | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1930-1490_1930-148 others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152215 | |||||||
chr18:70152278 | G | A | 89 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(86): Show |
90 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1930-1545C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152278 | |||||||
chr18:70152369 | T | A | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1930-1636A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152369 | |||||||
chr18:70152644 | G | A | 151 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(149): Show |
intron_variant | MODIFIER | c.1930-1911C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152644 | |||||||
chr18:70152705 | G | A | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1930-1972C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70152705 | |||||||
chr18:70153024 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1930-2291C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153024 | |||||||
chr18:70153032 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1930-2299G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153032 | |||||||
chr18:70153236 | C | CTA | 26 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(23): Show |
27 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1930-2505_1930-250 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153236 | |||||||
chr18:70153453 | T | C | 54 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(51): Show |
54 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1930-2720A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153453 | |||||||
chr18:70153601 | A | T | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1930-2868T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153601 | |||||||
chr18:70153697 | T | C | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1930-2964A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153697 | |||||||
chr18:70153707 | C | T | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1930-2974G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153707 | |||||||
chr18:70153930 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-3197A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153930 | |||||||
chr18:70153971 | A | G | 1 | a0003c0004t0003g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1930-3238T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70153971 | |||||||
chr18:70154044 | C | T | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-3311G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154044 | |||||||
chr18:70154104 | G | T | 1 | a0001c0005t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1930-3371C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154104 | |||||||
chr18:70154311 | G | T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-3578C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154311 | |||||||
chr18:70154412 | A | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-3679T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154412 | |||||||
chr18:70154536 | T | C | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1930-3803A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154536 | |||||||
chr18:70154699 | G | A | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1930-3966C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154699 | |||||||
chr18:70154727 | T | C | 1 | a0003c0004t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1930-3994A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154727 | |||||||
chr18:70154788 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-4055C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154788 | |||||||
chr18:70154964 | T | C | 1 | a0002c0001t0001g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1930-4231A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154964 | |||||||
chr18:70154999 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1930-4266A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70154999 | |||||||
chr18:70155324 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1930-4591G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155324 | |||||||
chr18:70155435 | AAT | A | 2 | a0001c0005t0001g0113 a0001c0005t0002g0112 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1930-4704_1930-470 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155435 | |||||||
chr18:70155633 | T | G | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1930-4900A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155633 | |||||||
chr18:70155674 | C | T | 1 | a0002c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1930-4941G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155674 | |||||||
chr18:70155679 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1930-4946C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155679 | |||||||
chr18:70155875 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-5142C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70155875 | |||||||
chr18:70156066 | A | C | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1930-5333T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156066 | |||||||
chr18:70156301 | C | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1930-5568G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156301 | |||||||
chr18:70156496 | A | G | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1930-5763T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156496 | |||||||
chr18:70156541 | T | C | 7 | a0002c0001t0005g0051 a0002c0001t0007g0059 a0002c0001t0007g0060 others(4): Show |
7 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1930-5808A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156541 | |||||||
chr18:70156550 | C | T | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1930-5817G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156550 | |||||||
chr18:70156670 | C | T | 89 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(86): Show |
90 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1930-5937G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156670 | |||||||
chr18:70156675 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-5942C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156675 | |||||||
chr18:70156744 | G | C | 1 | a0002c0001t0007g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1930-6011C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156744 | |||||||
chr18:70156949 | T | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-6216A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70156949 | |||||||
chr18:70157083 | A | C | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1930-6350T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157083 | |||||||
chr18:70157125 | G | A | 17 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1930-6392C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157125 | |||||||
chr18:70157129 | TTGCCCAT others(5): Show |
T | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-6408_1930-639 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157129 | |||||||
chr18:70157143 | C | G | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-6410G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157143 | |||||||
chr18:70157173 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1930-6440G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157173 | |||||||
chr18:70157178 | C | A | 60 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(57): Show |
60 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1930-6445G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157178 | |||||||
chr18:70157202 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1930-6469C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157202 | |||||||
chr18:70157203 | G | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1930-6470C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157203 | |||||||
chr18:70157409 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1930-6676G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157409 | |||||||
chr18:70157413 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1930-6680A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157413 | |||||||
chr18:70157452 | A | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1930-6719T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157452 | |||||||
chr18:70157734 | T | C | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-7001A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157734 | |||||||
chr18:70157916 | TA | T | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1930-7184delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70157916 | |||||||
chr18:70158077 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1930-7344C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158077 | |||||||
chr18:70158171 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1930-7438T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158171 | |||||||
chr18:70158182 | C | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1930-7449G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158182 | |||||||
chr18:70158214 | A | G | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1930-7481T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158214 | |||||||
chr18:70158393 | C | T | 95 | a0001c0002t0002g0038 a0001c0002t0004g0108 a0001c0002t0004g0121 others(92): Show |
96 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1930-7660G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158393 | |||||||
chr18:70158477 | T | C | 1 | a0002c0003t0001g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1929+7585A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158477 | |||||||
chr18:70158550 | A | G | 1 | a0002c0003t0001g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1929+7512T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158550 | |||||||
chr18:70158566 | A | G | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1929+7496T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158566 | |||||||
chr18:70158574 | A | G | 97 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1929+7488T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158574 | |||||||
chr18:70158891 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1929+7171A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158891 | |||||||
chr18:70158909 | A | AT | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1929+7152_1929+715 others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70158909 | |||||||
chr18:70159242 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+6820G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159242 | |||||||
chr18:70159519 | A | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1929+6543T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159519 | |||||||
chr18:70159664 | C | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1929+6398G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159664 | |||||||
chr18:70159696 | A | G | 93 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(90): Show |
94 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1929+6366T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159696 | |||||||
chr18:70159713 | C | A | 6 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(3): Show |
6 | HG00738.hp2 HG01981.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.1929+6349G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159713 | |||||||
chr18:70159766 | A | G | 1 | a0003c0004t0006g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1929+6296T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159766 | |||||||
chr18:70159994 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1929+6068A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70159994 | |||||||
chr18:70160106 | C | T | 9 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0074 others(6): Show |
9 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1929+5956G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160106 | |||||||
chr18:70160234 | C | G | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1929+5828G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160234 | |||||||
chr18:70160250 | T | C | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1929+5812A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160250 | |||||||
chr18:70160363 | GC | G | 60 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(57): Show |
60 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1929+5698delG | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160363 | |||||||
chr18:70160370 | A | G | 60 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(57): Show |
60 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1929+5692T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160370 | |||||||
chr18:70160514 | C | T | 1 | a0002c0001t0001g0084 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1929+5548G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160514 | |||||||
chr18:70160587 | A | C | 1 | a0002c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1929+5475T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160587 | |||||||
chr18:70160657 | G | GA | 17 | a0001c0023t0014g0155 a0003c0004t0003g0006 a0003c0004t0003g0007 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.1929+5404dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160657 | |||||||
chr18:70160657 | GA | G | 98 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1929+5404delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160657 | |||||||
chr18:70160726 | C | T | 2 | a0003c0004t0006g0014 a0003c0004t0006g0017 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1929+5336G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160726 | |||||||
chr18:70160764 | C | A | 4 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0001c0022t0004g0105 others(1): Show |
4 | HG00099.hp2 HG00639.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1929+5298G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160764 | |||||||
chr18:70160842 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1929+5220A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160842 | |||||||
chr18:70160975 | T | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+5087A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70160975 | |||||||
chr18:70161029 | C | T | 1 | a0001c0006t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1929+5033G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161029 | |||||||
chr18:70161129 | G | A | 2 | a0001c0013t0015g0127 a0001c0013t0016g0129 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1929+4933C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161129 | |||||||
chr18:70161186 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1929+4876A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161186 | |||||||
chr18:70161188 | T | C | 4 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG03225.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+4874A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161188 | |||||||
chr18:70161252 | C | T | 1 | a0001c0006t0021g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1929+4810G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161252 | |||||||
chr18:70161302 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1929+4760C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161302 | |||||||
chr18:70161316 | C | A | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1929+4746G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161316 | |||||||
chr18:70161460 | T | C | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1929+4602A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161460 | |||||||
chr18:70161552 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1929+4510T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161552 | |||||||
chr18:70161601 | T | C | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1929+4461A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161601 | |||||||
chr18:70161856 | G | A | 1 | a0001c0005t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1929+4206C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161856 | |||||||
chr18:70161891 | A | G | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+4171T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161891 | |||||||
chr18:70161924 | G | A | 90 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(87): Show |
91 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1929+4138C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161924 | |||||||
chr18:70161955 | G | A | 1 | a0003c0004t0003g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1929+4107C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70161955 | |||||||
chr18:70162285 | A | G | 2 | a0002c0003t0001g0047 a0002c0003t0001g0048 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1929+3777T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162285 | |||||||
chr18:70162289 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1929+3773C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162289 | |||||||
chr18:70162379 | C | T | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1929+3683G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162379 | |||||||
chr18:70162418 | G | A | 8 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(5): Show |
8 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1929+3644C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162418 | |||||||
chr18:70162457 | C | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1929+3605G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162457 | |||||||
chr18:70162622 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1929+3440C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162622 | |||||||
chr18:70162690 | G | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+3372C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162690 | |||||||
chr18:70162725 | C | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1929+3337G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162725 | |||||||
chr18:70162815 | A | AAACCC | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+3242_1929+324 others(9): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162815 | |||||||
chr18:70162885 | TG | T | 15 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1929+3176delC | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162885 | |||||||
chr18:70162886 | G | GA | 66 | a0001c0002t0001g0139 a0001c0007t0001g0145 a0001c0007t0001g0146 others(63): Show |
66 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1929+3175dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162886 | |||||||
chr18:70162886 | GA | G | 29 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(26): Show |
30 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1929+3175delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70162886 | |||||||
chr18:70163069 | T | TA | 16 | a0002c0001t0002g0103 a0002c0003t0001g0047 a0002c0003t0001g0067 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1929+2992dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TAA | 31 | a0001c0024t0012g0022 a0002c0001t0001g0073 a0002c0001t0001g0075 others(28): Show |
31 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1929+2991_1929+299 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TAAA | 17 | a0002c0001t0001g0072 a0002c0001t0001g0080 a0002c0001t0001g0089 others(14): Show |
17 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1929+2990_1929+299 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TAAAA | 7 | a0002c0001t0005g0051 a0002c0001t0005g0074 a0002c0001t0025g0045 others(4): Show |
7 | HG01106.hp2 HG01361.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+2989_1929+299 others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TAAAAAAA others(3): Show |
1 | a0001c0005t0027g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1929+2983_1929+299 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TAAAAAAA others(4): Show |
2 | a0001c0005t0010g0004 a0001c0005t0010g0005 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1929+2982_1929+299 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | T | TTAA | 5 | a0002c0001t0007g0059 a0002c0001t0007g0060 a0002c0001t0007g0061 others(2): Show |
5 | HG01981.hp2 HG02040.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1929+2992_1929+299 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | TA | T | 27 | a0001c0002t0001g0035 a0001c0002t0002g0025 a0001c0002t0002g0026 others(24): Show |
27 | HG01255.hp2 HG01346.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1929+2992delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | TAA | T | 8 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0124 others(5): Show |
9 | HG01106.hp1 HG01168.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1929+2991_1929+299 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | TAAA | T | 6 | a0001c0005t0001g0141 a0001c0006t0001g0123 a0001c0012t0018g0128 others(3): Show |
6 | HG02074.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1929+2990_1929+299 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | TAAAAAAA others(2): Show |
T | 7 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+2984_1929+299 others(13): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163069 | TAAAAAAA others(4): Show |
T | 1 | a0002c0001t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1929+2982_1929+299 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163069 | |||||||
chr18:70163083 | A | AC | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1929+2978_1929+297 others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163083 | |||||||
chr18:70163095 | A | C | 5 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0124 others(2): Show |
6 | HG01106.hp1 HG01168.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1929+2967T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163095 | |||||||
chr18:70163096 | A | C | 2 | a0001c0013t0015g0127 a0001c0013t0016g0129 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1929+2966T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163096 | |||||||
chr18:70163264 | C | T | 1 | a0002c0003t0001g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1929+2798G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163264 | |||||||
chr18:70163418 | G | A | 1 | a0001c0008t0008g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1929+2644C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163418 | |||||||
chr18:70163595 | T | C | 1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1929+2467A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163595 | |||||||
chr18:70163839 | G | A | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+2223C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70163839 | |||||||
chr18:70164149 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1929+1913C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164149 | |||||||
chr18:70164154 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+1908A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164154 | |||||||
chr18:70164210 | CTT | C | 36 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(33): Show |
37 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1929+1850_1929+185 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164210 | |||||||
chr18:70164210 | CTTT | C | 56 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(53): Show |
56 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1929+1849_1929+185 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164210 | |||||||
chr18:70164239 | TA | T | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1929+1822delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164239 | |||||||
chr18:70164292 | A | ACCTTGAC others(3): Show |
93 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(90): Show |
94 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1929+1760_1929+176 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164292 | |||||||
chr18:70164366 | C | T | 4 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0018 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+1696G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164366 | |||||||
chr18:70164377 | A | AT | 5 | a0001c0008t0008g0116 a0001c0011t0004g0151 a0001c0011t0004g0152 others(2): Show |
5 | HG00099.hp2 HG00639.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1929+1684dupA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164377 | |||||||
chr18:70164550 | C | CA | 94 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(91): Show |
95 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1929+1511dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164550 | |||||||
chr18:70164957 | A | C | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1929+1105T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70164957 | |||||||
chr18:70165086 | A | G | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1929+976T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165086 | |||||||
chr18:70165207 | A | C | 28 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(25): Show |
29 | HG01106.hp1 HG01109.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1929+855T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165207 | |||||||
chr18:70165286 | A | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+776T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165286 | |||||||
chr18:70165338 | TACA | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1929+721_1929+723d others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165338 | |||||||
chr18:70165375 | T | G | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1929+687A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165375 | |||||||
chr18:70165505 | T | C | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+557A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165505 | |||||||
chr18:70165712 | A | T | 1 | a0002c0003t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1929+350T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165712 | |||||||
chr18:70165737 | C | T | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1929+325G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165737 | |||||||
chr18:70165966 | T | C | 1 | a0001c0006t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1929+96A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70165966 | |||||||
chr18:70166044 | G | A | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1929+18C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70166044 | |||||||
chr18:70166059 | C | T | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.1929+3G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 14/48 | chr18 | 70166059 | |||||||
chr18:70166429 | T | G | 3 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 |
3 | HG02723.hp2 HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1803-241A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 13/48 | chr18 | 70166429 | |||||||
chr18:70166508 | C | T | 4 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
4 | HG03225.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803-320G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 13/48 | chr18 | 70166508 | |||||||
chr18:70167195 | G | T | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1690-164C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167195 | |||||||
chr18:70167259 | C | G | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1690-228G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167259 | |||||||
chr18:70167336 | G | A | 3 | a0002c0003t0001g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 |
3 | HG02451.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1690-305C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167336 | |||||||
chr18:70167465 | G | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1690-434C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167465 | |||||||
chr18:70167703 | CA | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-673delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167703 | |||||||
chr18:70167947 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1689+908C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70167947 | |||||||
chr18:70168041 | A | G | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1689+814T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168041 | |||||||
chr18:70168053 | C | T | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1689+802G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168053 | |||||||
chr18:70168060 | A | C | 27 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(24): Show |
28 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1689+795T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168060 | |||||||
chr18:70168073 | A | C | 1 | a0002c0001t0005g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1689+782T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168073 | |||||||
chr18:70168113 | C | CAAA | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1689+739_1689+741d others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168113 | |||||||
chr18:70168191 | A | G | 4 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0018 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+664T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168191 | |||||||
chr18:70168422 | A | G | 1 | a0001c0006t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1689+433T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168422 | |||||||
chr18:70168487 | C | T | 4 | a0002c0003t0001g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+368G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168487 | |||||||
chr18:70168529 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1689+326A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168529 | |||||||
chr18:70168664 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1689+191C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168664 | |||||||
chr18:70168768 | T | G | 1 | a0002c0001t0007g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1689+87A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168768 | |||||||
chr18:70168812 | T | C | 1 | a0001c0002t0002g0036 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1689+43A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 12/48 | chr18 | 70168812 | |||||||
chr18:70169212 | A | T | 2 | a0002c0003t0001g0047 a0002c0003t0001g0048 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1477-145T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70169212 | |||||||
chr18:70169264 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1477-197T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70169264 | |||||||
chr18:70169385 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1477-318C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70169385 | |||||||
chr18:70169432 | C | T | 1 | a0001c0002t0002g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1477-365G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70169432 | |||||||
chr18:70170005 | T | C | 106 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(103): Show |
107 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1477-938A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170005 | |||||||
chr18:70170281 | C | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1477-1214G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170281 | |||||||
chr18:70170292 | C | T | 2 | a0001c0002t0002g0028 a0001c0002t0002g0038 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1477-1225G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170292 | |||||||
chr18:70170293 | G | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477-1226C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170293 | |||||||
chr18:70170411 | A | G | 1 | a0002c0001t0001g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1477-1344T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170411 | |||||||
chr18:70170432 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477-1365C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170432 | |||||||
chr18:70170555 | G | A | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1477-1488C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170555 | |||||||
chr18:70170662 | G | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1477-1595C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170662 | |||||||
chr18:70170803 | G | C | 2 | a0002c0001t0001g0078 a0005c0015t0001g0069 |
2 | HG01257.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1477-1736C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70170803 | |||||||
chr18:70171031 | TG | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1477-1965delC | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70171031 | |||||||
chr18:70171080 | A | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1477-2013T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70171080 | |||||||
chr18:70171851 | T | A | 1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1477-2784A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70171851 | |||||||
chr18:70172185 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-3118A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172185 | |||||||
chr18:70172302 | A | G | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477-3235T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172302 | |||||||
chr18:70172558 | T | C | 17 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1477-3491A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172558 | |||||||
chr18:70172692 | T | TA | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1477-3626dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172692 | |||||||
chr18:70172720 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1477-3653A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172720 | |||||||
chr18:70172854 | G | A | 1 | a0002c0001t0001g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1477-3787C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172854 | |||||||
chr18:70172925 | T | A | 1 | a0001c0002t0002g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1476+3750A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70172925 | |||||||
chr18:70173165 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+3510G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173165 | |||||||
chr18:70173220 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+3455G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173220 | |||||||
chr18:70173264 | G | A | 10 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(7): Show |
11 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1476+3411C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173264 | |||||||
chr18:70173277 | G | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+3398C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173277 | |||||||
chr18:70173425 | G | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1476+3250C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173425 | |||||||
chr18:70173491 | C | CA | 14 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1476+3183dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173491 | |||||||
chr18:70173521 | G | A | 1 | a0001c0002t0002g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1476+3154C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173521 | |||||||
chr18:70173531 | T | C | 27 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(24): Show |
27 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1476+3144A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173531 | |||||||
chr18:70173750 | C | G | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1476+2925G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173750 | |||||||
chr18:70173762 | C | T | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1476+2913G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70173762 | |||||||
chr18:70174060 | T | C | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1476+2615A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174060 | |||||||
chr18:70174147 | TA | T | 70 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(67): Show |
70 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1476+2527delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174147 | |||||||
chr18:70174147 | TAAA | T | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1476+2525_1476+252 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174147 | |||||||
chr18:70174335 | G | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1476+2340C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174335 | |||||||
chr18:70174472 | T | C | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.1476+2203A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174472 | |||||||
chr18:70174489 | T | C | 25 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(22): Show |
25 | HG01081.hp2 HG01109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1476+2186A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174489 | |||||||
chr18:70174525 | G | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1476+2150C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174525 | |||||||
chr18:70174611 | G | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+2064C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174611 | |||||||
chr18:70174726 | A | G | 32 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(29): Show |
33 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1476+1949T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174726 | |||||||
chr18:70174842 | G | A | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1476+1833C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174842 | |||||||
chr18:70174858 | TA | T | 34 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(31): Show |
35 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1476+1816delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70174858 | |||||||
chr18:70175045 | C | CA | 120 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(117): Show |
121 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.1476+1629dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175045 | |||||||
chr18:70175045 | C | CAA | 17 | a0001c0005t0001g0113 a0001c0005t0002g0112 a0001c0006t0001g0124 others(14): Show |
17 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1476+1628_1476+162 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175045 | |||||||
chr18:70175077 | C | T | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1476+1598G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175077 | |||||||
chr18:70175372 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1476+1303G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175372 | |||||||
chr18:70175545 | T | G | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+1130A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175545 | |||||||
chr18:70175571 | A | T | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1476+1104T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175571 | |||||||
chr18:70175580 | A | C | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1476+1095T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175580 | |||||||
chr18:70175627 | T | C | 1 | a0002c0001t0001g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1476+1048A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175627 | |||||||
chr18:70175633 | CA | C | 150 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(147): Show |
151 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(148): Show |
intron_variant | MODIFIER | c.1476+1041delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175633 | |||||||
chr18:70175734 | A | T | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+941T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175734 | |||||||
chr18:70175868 | T | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1476+807A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175868 | |||||||
chr18:70175903 | T | C | 1 | a0002c0001t0001g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1476+772A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70175903 | |||||||
chr18:70176084 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+591A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176084 | |||||||
chr18:70176146 | AAAG | A | 19 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+526_1476+528d others(5): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176146 | |||||||
chr18:70176184 | C | CGTAGAT | 4 | a0001c0007t0001g0150 a0001c0010t0001g0132 a0001c0010t0004g0133 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1476+485_1476+490d others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176184 | |||||||
chr18:70176184 | CGTAGAT | C | 29 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(26): Show |
30 | HG00639.hp1 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1476+485_1476+490d others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176184 | |||||||
chr18:70176188 | GATGTAGA others(11): Show |
G | 1 | a0001c0011t0004g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1476+469_1476+486d others(20): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176188 | |||||||
chr18:70176194 | G | T | 1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1476+481C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176194 | |||||||
chr18:70176194 | GATGTAGA others(11): Show |
G | 3 | a0001c0013t0015g0127 a0001c0013t0016g0129 a0002c0003t0001g0057 |
3 | HG02647.hp2 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1476+463_1476+480d others(20): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176194 | |||||||
chr18:70176194 | GATGTAGA others(17): Show |
G | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1476+457_1476+480d others(26): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176194 | |||||||
chr18:70176200 | G | GATGTAT | 18 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(15): Show |
18 | HG01081.hp2 HG02300.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1476+469_1476+474d others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | G | GATGTATA others(5): Show |
1 | a0001c0006t0020g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1476+463_1476+474d others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | G | GATGTATA others(17): Show |
2 | a0003c0004t0006g0017 a0004c0026t0004g0143 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1476+451_1476+474d others(26): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | G | T | 3 | a0001c0005t0001g0141 a0001c0011t0004g0151 a0002c0017t0002g0102 |
3 | HG00639.hp1 HG02615.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1476+475C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | GATGTAT | G | 36 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0005t0001g0109 others(33): Show |
37 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1476+469_1476+474d others(8): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | GATGTATA others(5): Show |
G | 32 | a0001c0002t0002g0025 a0001c0002t0002g0027 a0001c0002t0002g0034 others(29): Show |
32 | HG00621.hp1 HG00738.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1476+463_1476+474d others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | GATGTATA others(11): Show |
G | 17 | a0001c0002t0001g0035 a0001c0002t0002g0026 a0001c0002t0002g0028 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1476+457_1476+474d others(20): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176200 | GATGTATA others(17): Show |
G | 7 | a0001c0002t0001g0139 a0001c0002t0002g0134 a0001c0002t0002g0135 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+451_1476+474d others(26): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176200 | |||||||
chr18:70176206 | T | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0147 a0001c0007t0001g0148 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+469A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176206 | |||||||
chr18:70176212 | T | G | 3 | a0001c0007t0001g0146 a0002c0001t0001g0095 a0002c0001t0001g0096 |
3 | HG01981.hp1 HG02145.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1476+463A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176212 | |||||||
chr18:70176218 | T | G | 2 | a0001c0021t0017g0131 a0002c0001t0001g0100 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1476+457A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176218 | |||||||
chr18:70176376 | CAATA | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1476+295_1476+298d others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 11/48 | chr18 | 70176376 | |||||||
chr18:70177050 | A | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306-205T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177050 | |||||||
chr18:70177052 | A | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1306-207T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177052 | |||||||
chr18:70177229 | C | A | 1 | a0002c0003t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306-384G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177229 | |||||||
chr18:70177269 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-424A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177269 | |||||||
chr18:70177270 | A | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-425T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177270 | |||||||
chr18:70177282 | A | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306-437T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177282 | |||||||
chr18:70177298 | T | C | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306-453A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177298 | |||||||
chr18:70177326 | A | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306-481T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177326 | |||||||
chr18:70177789 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-944C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177789 | |||||||
chr18:70177959 | G | T | 81 | a0001c0002t0001g0035 a0001c0002t0002g0025 a0001c0002t0002g0026 others(78): Show |
81 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1306-1114C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177959 | |||||||
chr18:70177965 | A | G | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1306-1120T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177965 | |||||||
chr18:70177967 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1306-1122T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70177967 | |||||||
chr18:70178102 | G | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-1257C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178102 | |||||||
chr18:70178249 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1306-1404C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178249 | |||||||
chr18:70178424 | T | C | 12 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(9): Show |
13 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1306-1579A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178424 | |||||||
chr18:70178488 | T | C | 25 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(22): Show |
25 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1306-1643A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178488 | |||||||
chr18:70178589 | AT | A | 7 | a0002c0003t0001g0063 a0002c0003t0001g0065 a0002c0003t0001g0066 others(4): Show |
7 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1306-1745delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178589 | |||||||
chr18:70178705 | A | C | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306-1860T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178705 | |||||||
chr18:70178969 | G | C | 3 | a0001c0005t0010g0004 a0001c0005t0010g0005 a0001c0005t0027g0023 |
3 | HG02559.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1306-2124C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70178969 | |||||||
chr18:70179364 | C | T | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1306-2519G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70179364 | |||||||
chr18:70179596 | TG | T | 15 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(12): Show |
15 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1306-2752delC | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70179596 | |||||||
chr18:70179769 | G | C | 33 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(30): Show |
33 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1306-2924C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70179769 | |||||||
chr18:70179998 | C | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1306-3153G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70179998 | |||||||
chr18:70180010 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-3165A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180010 | |||||||
chr18:70180030 | C | A | 1 | a0001c0005t0010g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306-3185G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180030 | |||||||
chr18:70180059 | C | T | 5 | a0002c0003t0001g0049 a0002c0003t0001g0052 a0002c0003t0001g0055 others(2): Show |
5 | HG01884.hp1 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-3214G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180059 | |||||||
chr18:70180087 | A | G | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306-3242T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180087 | |||||||
chr18:70180121 | TA | T | 35 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(32): Show |
36 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1306-3277delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180121 | |||||||
chr18:70180155 | A | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1306-3310T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180155 | |||||||
chr18:70180327 | T | G | 1 | a0003c0004t0006g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1306-3482A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180327 | |||||||
chr18:70180514 | G | A | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1306-3669C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180514 | |||||||
chr18:70180539 | G | A | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1306-3694C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180539 | |||||||
chr18:70180591 | G | GA | 16 | a0002c0001t0001g0072 a0002c0001t0001g0075 a0002c0001t0001g0076 others(13): Show |
16 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1306-3747dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180591 | |||||||
chr18:70180770 | A | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1306-3925T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70180770 | |||||||
chr18:70181254 | A | G | 17 | a0003c0004t0003g0006 a0003c0004t0003g0007 a0003c0004t0003g0008 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1306-4409T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70181254 | |||||||
chr18:70181357 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306-4512A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70181357 | |||||||
chr18:70181762 | T | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1306-4917A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70181762 | |||||||
chr18:70181841 | G | A | 1 | a0002c0001t0005g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1306-4996C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70181841 | |||||||
chr18:70181962 | T | C | 1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1306-5117A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70181962 | |||||||
chr18:70182361 | G | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1306-5516C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182361 | |||||||
chr18:70182380 | G | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-5535C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182380 | |||||||
chr18:70182423 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1306-5578C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182423 | |||||||
chr18:70182545 | A | G | 32 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(29): Show |
33 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1305+5563T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182545 | |||||||
chr18:70182818 | C | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1305+5290G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182818 | |||||||
chr18:70182986 | C | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+5122G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70182986 | |||||||
chr18:70183096 | A | G | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1305+5012T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183096 | |||||||
chr18:70183321 | A | T | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1305+4787T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183321 | |||||||
chr18:70183538 | G | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+4570C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183538 | |||||||
chr18:70183609 | C | T | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+4499G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183609 | |||||||
chr18:70183663 | C | T | 2 | a0003c0004t0003g0009 a0003c0004t0003g0021 |
2 | HG01081.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1305+4445G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183663 | |||||||
chr18:70183964 | T | TA | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1305+4143dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70183964 | |||||||
chr18:70184351 | C | T | 1 | a0003c0004t0003g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1305+3757G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184351 | |||||||
chr18:70184516 | C | T | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+3592G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184516 | |||||||
chr18:70184526 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1305+3582A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184526 | |||||||
chr18:70184703 | G | GTTTTTTT | 9 | a0002c0001t0007g0059 a0002c0003t0001g0049 a0002c0003t0001g0052 others(6): Show |
9 | HG01106.hp2 HG01884.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305+3398_1305+340 others(11): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184703 | G | GTTTTTTT others(2): Show |
8 | a0001c0009t0001g0039 a0002c0003t0001g0047 a0002c0003t0001g0048 others(5): Show |
8 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+3396_1305+340 others(13): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184703 | G | GTTTTTTT others(8): Show |
1 | a0001c0011t0004g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1305+3404_1305+340 others(19): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184703 | GT | G | 7 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(4): Show |
8 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305+3404delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184703 | GTTT | G | 5 | a0001c0006t0020g0120 a0001c0008t0008g0115 a0001c0008t0008g0118 others(2): Show |
5 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+3402_1305+340 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184703 | GTTTTTTT others(2): Show |
G | 7 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1305+3396_1305+340 others(13): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184703 | |||||||
chr18:70184706 | T | G | 1 | a0001c0013t0015g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1305+3402A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184706 | |||||||
chr18:70184706 | T | TGTG | 2 | a0001c0006t0001g0126 a0001c0013t0016g0129 |
2 | HG03098.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1305+3401_1305+340 others(7): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184706 | |||||||
chr18:70184707 | TTTTTTTT others(6): Show |
T | 3 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 |
3 | HG02970.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1305+3388_1305+340 others(17): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184707 | |||||||
chr18:70184707 | TTTTTTTT others(18): Show |
T | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+3376_1305+340 others(29): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184707 | |||||||
chr18:70184708 | T | G | 9 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(6): Show |
10 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1305+3400A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184708 | |||||||
chr18:70184710 | T | G | 15 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(12): Show |
16 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1305+3398A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184710 | |||||||
chr18:70184712 | T | G | 17 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(14): Show |
18 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1305+3396A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184712 | |||||||
chr18:70184713 | T | G | 1 | a0002c0001t0004g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1305+3395A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184713 | |||||||
chr18:70184714 | T | G | 19 | a0001c0005t0001g0141 a0001c0006t0001g0001 a0001c0006t0001g0122 others(16): Show |
20 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1305+3394A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184714 | |||||||
chr18:70184714 | T | TTGTGTGT others(5): Show |
1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1305+3393_1305+339 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184714 | |||||||
chr18:70184716 | T | G | 25 | a0001c0002t0002g0027 a0001c0002t0002g0029 a0001c0002t0002g0034 others(22): Show |
26 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1305+3392A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TGTGTGTG others(4): Show |
2 | a0001c0002t0002g0025 a0001c0002t0002g0037 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTGTGTGT others(5): Show |
3 | a0001c0002t0002g0135 a0001c0002t0002g0136 a0001c0021t0017g0131 |
3 | HG01255.hp2 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1305+3380_1305+339 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTGTGTGT others(7): Show |
1 | a0001c0024t0012g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1305+3378_1305+339 others(18): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTGTGT others(3): Show |
2 | a0001c0002t0002g0137 a0001c0002t0002g0138 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTGTGT others(5): Show |
1 | a0001c0002t0002g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTGTG others(4): Show |
4 | a0001c0002t0001g0139 a0001c0002t0002g0038 a0002c0001t0005g0094 others(1): Show |
4 | HG00621.hp1 HG02145.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTGT others(3): Show |
1 | a0002c0001t0007g0083 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTGT others(7): Show |
1 | a0001c0002t0002g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(18): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTG others(4): Show |
3 | a0001c0002t0001g0035 a0001c0002t0002g0031 a0001c0002t0002g0032 |
3 | HG03225.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTG others(6): Show |
2 | a0002c0001t0001g0098 a0002c0001t0013g0070 |
2 | HG00621.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(17): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(5): Show |
4 | a0002c0001t0001g0096 a0002c0001t0005g0074 a0002c0001t0009g0099 others(1): Show |
4 | HG00738.hp1 HG01257.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(7): Show |
2 | a0001c0002t0002g0134 a0002c0003t0026g0101 |
2 | HG01361.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(18): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(4): Show |
2 | a0001c0002t0002g0028 a0002c0001t0011g0085 |
2 | HG01981.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(15): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(6): Show |
4 | a0002c0001t0001g0076 a0002c0001t0001g0080 a0002c0001t0001g0084 others(1): Show |
4 | HG00099.hp1 HG02074.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(17): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(8): Show |
5 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0079 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(19): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(3): Show |
1 | a0001c0009t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(14): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(6): Show |
5 | a0002c0001t0001g0078 a0002c0001t0001g0089 a0002c0001t0001g0095 others(2): Show |
5 | HG01346.hp1 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305+3391_1305+339 others(17): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(5): Show |
1 | a0002c0001t0002g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(16): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(7): Show |
1 | a0002c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(18): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(8): Show |
1 | a0002c0017t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(19): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(10): Show |
1 | a0001c0011t0004g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(21): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(11): Show |
1 | a0001c0010t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(22): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | T | TTTTTTTT others(12): Show |
1 | a0001c0010t0004g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1305+3391_1305+339 others(23): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184716 | TTG | T | 8 | a0003c0004t0003g0002 a0003c0004t0003g0003 a0003c0004t0003g0006 others(5): Show |
8 | HG01081.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1305+3390_1305+339 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184716 | |||||||
chr18:70184718 | G | T | 24 | a0002c0003t0001g0047 a0002c0003t0001g0048 a0002c0003t0001g0049 others(21): Show |
24 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1305+3390C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184718 | |||||||
chr18:70184720 | G | T | 12 | a0002c0003t0001g0047 a0002c0003t0001g0048 a0002c0003t0001g0055 others(9): Show |
12 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1305+3388C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184720 | |||||||
chr18:70184722 | G | T | 1 | a0002c0016t0001g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1305+3386C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184722 | |||||||
chr18:70184764 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1305+3344C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184764 | |||||||
chr18:70184851 | C | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1305+3257G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184851 | |||||||
chr18:70184863 | C | T | 5 | a0001c0005t0002g0106 a0001c0005t0002g0107 a0001c0005t0010g0004 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305+3245G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184863 | |||||||
chr18:70184889 | A | C | 41 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(38): Show |
42 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1305+3219T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184889 | |||||||
chr18:70184911 | G | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+3197C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70184911 | |||||||
chr18:70185069 | C | T | 28 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(25): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1305+3039G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185069 | |||||||
chr18:70185180 | G | A | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+2928C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185180 | |||||||
chr18:70185280 | A | G | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1305+2828T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185280 | |||||||
chr18:70185300 | G | C | 13 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(10): Show |
13 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1305+2808C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185300 | |||||||
chr18:70185471 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1305+2637A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185471 | |||||||
chr18:70185599 | A | G | 1 | a0001c0002t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1305+2509T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185599 | |||||||
chr18:70185748 | A | G | 41 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(38): Show |
42 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1305+2360T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185748 | |||||||
chr18:70185807 | T | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1305+2301A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185807 | |||||||
chr18:70185823 | G | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1305+2285C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185823 | |||||||
chr18:70185832 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1305+2276A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185832 | |||||||
chr18:70185897 | T | C | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1305+2211A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185897 | |||||||
chr18:70185953 | T | A | 1 | a0002c0001t0005g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1305+2155A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70185953 | |||||||
chr18:70186049 | T | C | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1305+2059A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186049 | |||||||
chr18:70186080 | C | A | 1 | a0001c0006t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1305+2028G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186080 | |||||||
chr18:70186080 | C | CA | 33 | a0001c0002t0001g0139 a0001c0002t0002g0034 a0001c0002t0004g0108 others(30): Show |
33 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1305+2027dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186080 | |||||||
chr18:70186080 | C | T | 5 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(2): Show |
6 | HG01168.hp2 HG02074.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+2028G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186080 | |||||||
chr18:70186249 | A | C | 1 | a0001c0008t0008g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1305+1859T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186249 | |||||||
chr18:70186636 | G | A | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1305+1472C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186636 | |||||||
chr18:70186838 | G | A | 6 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305+1270C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186838 | |||||||
chr18:70186846 | T | C | 7 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305+1262A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186846 | |||||||
chr18:70186917 | G | C | 10 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(7): Show |
10 | HG00099.hp2 HG00639.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305+1191C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186917 | |||||||
chr18:70186978 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1305+1130G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70186978 | |||||||
chr18:70187145 | G | T | 1 | a0002c0001t0007g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1305+963C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187145 | |||||||
chr18:70187218 | G | C | 21 | a0001c0002t0001g0035 a0001c0002t0002g0025 a0001c0002t0002g0026 others(18): Show |
21 | HG01346.hp2 HG01884.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1305+890C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187218 | |||||||
chr18:70187460 | A | G | 7 | a0001c0002t0001g0139 a0001c0002t0002g0134 a0001c0002t0002g0135 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1305+648T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187460 | |||||||
chr18:70187484 | T | C | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1305+624A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187484 | |||||||
chr18:70187518 | C | T | 8 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0001c0002t0002g0027 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+590G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187518 | |||||||
chr18:70187538 | T | C | 28 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(25): Show |
28 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1305+570A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187538 | |||||||
chr18:70187552 | C | T | 1 | a0002c0003t0001g0052 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1305+556G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187552 | |||||||
chr18:70187812 | G | A | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1305+296C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 10/48 | chr18 | 70187812 | |||||||
chr18:70188688 | A | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1190-465T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70188688 | |||||||
chr18:70188865 | A | AC | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1190-643dupG | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70188865 | |||||||
chr18:70188893 | T | C | 1 | a0001c0005t0001g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1190-670A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70188893 | |||||||
chr18:70188986 | G | A | 1 | a0001c0007t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1190-763C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70188986 | |||||||
chr18:70189390 | T | C | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1189+1148A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70189390 | |||||||
chr18:70189392 | A | C | 1 | a0002c0001t0001g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1189+1146T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70189392 | |||||||
chr18:70189663 | A | C | 2 | a0002c0001t0011g0085 a0002c0019t0011g0058 |
2 | HG01981.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+875T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70189663 | |||||||
chr18:70189756 | G | A | 1 | a0005c0015t0001g0069 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1189+782C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70189756 | |||||||
chr18:70189889 | T | C | 31 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(28): Show |
32 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1189+649A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70189889 | |||||||
chr18:70190191 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1189+347A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70190191 | |||||||
chr18:70190242 | T | A | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1189+296A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70190242 | |||||||
chr18:70190482 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1189+56G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 9/48 | chr18 | 70190482 | |||||||
chr18:70190723 | C | A | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
splice_region_variant&intron_variant | LOW | c.1008-4G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70190723 | |||||||
chr18:70190849 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008-130G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70190849 | |||||||
chr18:70190856 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1008-137C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70190856 | |||||||
chr18:70191013 | T | C | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1008-294A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191013 | |||||||
chr18:70191069 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1008-350G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191069 | |||||||
chr18:70191234 | A | G | 28 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(25): Show |
28 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1008-515T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191234 | |||||||
chr18:70191362 | T | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1008-643A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191362 | |||||||
chr18:70191704 | C | T | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.1008-985G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191704 | |||||||
chr18:70191716 | A | G | 2 | a0003c0004t0003g0006 a0003c0004t0003g0007 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1008-997T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191716 | |||||||
chr18:70191768 | C | T | 8 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0005g0082 others(5): Show |
8 | HG00621.hp1 HG00735.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008-1049G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191768 | |||||||
chr18:70191949 | CAT | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1008-1232_1008-123 others(6): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70191949 | |||||||
chr18:70192206 | T | C | 1 | a0002c0001t0005g0082 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1007+1082A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192206 | |||||||
chr18:70192308 | A | G | 104 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.1007+980T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192308 | |||||||
chr18:70192443 | G | A | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1007+845C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192443 | |||||||
chr18:70192464 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1007+824A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192464 | |||||||
chr18:70192529 | G | C | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1007+759C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192529 | |||||||
chr18:70192565 | C | A | 1 | a0001c0002t0002g0037 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1007+723G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192565 | |||||||
chr18:70192625 | G | A | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1007+663C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192625 | |||||||
chr18:70192669 | CA | C | 55 | a0001c0022t0004g0105 a0002c0001t0001g0072 a0002c0001t0001g0073 others(52): Show |
55 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1007+618delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192669 | |||||||
chr18:70192669 | CAA | C | 8 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007+617_1007+618d others(4): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192669 | |||||||
chr18:70192685 | A | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1007+603T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192685 | |||||||
chr18:70192690 | G | T | 2 | a0004c0025t0001g0144 a0004c0026t0004g0143 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1007+598C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192690 | |||||||
chr18:70192722 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1007+566T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192722 | |||||||
chr18:70192952 | T | A | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1007+336A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192952 | |||||||
chr18:70192977 | C | G | 1 | a0001c0006t0001g0122 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1007+311G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70192977 | |||||||
chr18:70193050 | A | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1007+238T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70193050 | |||||||
chr18:70193082 | G | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1007+206C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70193082 | |||||||
chr18:70193083 | C | T | 28 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(25): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1007+205G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70193083 | |||||||
chr18:70193176 | CA | C | 33 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(30): Show |
33 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007+111delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70193176 | |||||||
chr18:70193176 | CAAAAAAA others(3): Show |
C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1007+102_1007+111d others(12): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 8/48 | chr18 | 70193176 | |||||||
chr18:70193483 | T | C | 133 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.842-30A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70193483 | |||||||
chr18:70193487 | TA | T | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.842-35delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70193487 | |||||||
chr18:70193827 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.842-374G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70193827 | |||||||
chr18:70193881 | G | A | 1 | a0001c0009t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.842-428C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70193881 | |||||||
chr18:70193937 | G | A | 1 | a0002c0018t0005g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.842-484C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70193937 | |||||||
chr18:70194004 | T | C | 1 | a0002c0001t0001g0084 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.842-551A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70194004 | |||||||
chr18:70194113 | T | C | 63 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(60): Show |
63 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.842-660A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70194113 | |||||||
chr18:70194174 | T | C | 1 | a0003c0004t0006g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.842-721A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70194174 | |||||||
chr18:70194702 | G | A | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.842-1249C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70194702 | |||||||
chr18:70194988 | G | T | 62 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(59): Show |
62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.841+1513C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70194988 | |||||||
chr18:70195021 | A | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.841+1480T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195021 | |||||||
chr18:70195066 | T | C | 1 | a0001c0006t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.841+1435A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195066 | |||||||
chr18:70195311 | T | C | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.841+1190A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195311 | |||||||
chr18:70195357 | T | C | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.841+1144A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195357 | |||||||
chr18:70195389 | T | C | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.841+1112A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195389 | |||||||
chr18:70195582 | G | C | 31 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(28): Show |
32 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.841+919C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195582 | |||||||
chr18:70195627 | C | T | 1 | a0002c0001t0013g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.841+874G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195627 | |||||||
chr18:70195814 | T | G | 1 | a0002c0001t0007g0061 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.841+687A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70195814 | |||||||
chr18:70196021 | T | C | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.841+480A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70196021 | |||||||
chr18:70196296 | GA | G | 66 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0001t0001g0072 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.841+204delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70196296 | |||||||
chr18:70196341 | C | T | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.841+160G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70196341 | |||||||
chr18:70196490 | A | G | 2 | a0001c0006t0020g0120 a0001c0006t0021g0119 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.841+11T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 7/48 | chr18 | 70196490 | |||||||
chr18:70196657 | A | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.694-9T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70196657 | |||||||
chr18:70196667 | G | A | 4 | a0001c0012t0018g0128 a0001c0012t0019g0130 a0001c0013t0015g0127 others(1): Show |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-19C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70196667 | |||||||
chr18:70196722 | A | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.694-74T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70196722 | |||||||
chr18:70196921 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.694-273C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70196921 | |||||||
chr18:70197026 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.694-378C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197026 | |||||||
chr18:70197048 | G | A | 1 | a0001c0005t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.694-400C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197048 | |||||||
chr18:70197162 | T | C | 1 | a0002c0001t0025g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.693+462A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197162 | |||||||
chr18:70197294 | G | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693+330C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197294 | |||||||
chr18:70197481 | T | C | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693+143A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197481 | |||||||
chr18:70197534 | T | A | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.693+90A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 6/48 | chr18 | 70197534 | |||||||
chr18:70197805 | G | A | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.579-67C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70197805 | |||||||
chr18:70197877 | T | C | 1 | a0006c0014t0022g0046 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.579-139A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70197877 | |||||||
chr18:70198077 | T | C | 10 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-339A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198077 | |||||||
chr18:70198124 | T | C | 1 | a0002c0001t0011g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.579-386A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198124 | |||||||
chr18:70198242 | G | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.579-504C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198242 | |||||||
chr18:70198259 | T | C | 8 | a0002c0003t0001g0063 a0002c0003t0001g0064 a0002c0003t0001g0065 others(5): Show |
8 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.579-521A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198259 | |||||||
chr18:70198476 | C | T | 28 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(25): Show |
29 | HG01106.hp1 HG01168.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-738G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198476 | |||||||
chr18:70198626 | C | T | 134 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.578+788G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198626 | |||||||
chr18:70198700 | C | T | 7 | a0001c0002t0001g0139 a0001c0002t0002g0134 a0001c0002t0002g0135 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+714G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198700 | |||||||
chr18:70198799 | T | G | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.578+615A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198799 | |||||||
chr18:70198930 | G | T | 31 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(28): Show |
32 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.578+484C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70198930 | |||||||
chr18:70199048 | G | C | 1 | a0002c0001t0001g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.578+366C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70199048 | |||||||
chr18:70199102 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.578+312C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70199102 | |||||||
chr18:70199299 | A | T | 6 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0012t0018g0128 others(3): Show |
6 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.578+115T>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70199299 | |||||||
chr18:70199399 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+15G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 5/48 | chr18 | 70199399 | |||||||
chr18:70199519 | G | A | 1 | a0002c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.488-15C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70199519 | |||||||
chr18:70199696 | A | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.488-192T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70199696 | |||||||
chr18:70199986 | G | A | 1 | a0002c0003t0001g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.488-482C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70199986 | |||||||
chr18:70200427 | G | A | 61 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(58): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.488-923C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70200427 | |||||||
chr18:70200443 | C | T | 1 | a0001c0013t0015g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.488-939G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70200443 | |||||||
chr18:70200583 | G | A | 1 | a0001c0009t0004g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.488-1079C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70200583 | |||||||
chr18:70201205 | A | C | 2 | a0001c0010t0001g0132 a0001c0010t0004g0133 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.487+689T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201205 | |||||||
chr18:70201219 | C | T | 1 | a0002c0001t0009g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.487+675G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201219 | |||||||
chr18:70201229 | C | A | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+665G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201229 | |||||||
chr18:70201269 | A | G | 2 | a0001c0021t0017g0131 a0001c0024t0012g0022 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.487+625T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201269 | |||||||
chr18:70201321 | G | A | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+573C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201321 | |||||||
chr18:70201325 | G | A | 4 | a0002c0001t0001g0100 a0002c0001t0009g0090 a0002c0001t0009g0091 others(1): Show |
4 | HG00738.hp1 HG01109.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+569C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201325 | |||||||
chr18:70201325 | G | T | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+569C>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201325 | |||||||
chr18:70201329 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.487+565C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201329 | |||||||
chr18:70201399 | G | A | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.487+495C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201399 | |||||||
chr18:70201464 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+430A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201464 | |||||||
chr18:70201481 | G | A | 1 | a0002c0003t0026g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+413C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201481 | |||||||
chr18:70201500 | T | C | 1 | a0001c0002t0004g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.487+394A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201500 | |||||||
chr18:70201536 | A | G | 1 | a0002c0001t0004g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.487+358T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201536 | |||||||
chr18:70201541 | G | A | 1 | a0002c0003t0001g0068 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.487+353C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201541 | |||||||
chr18:70201607 | C | CA | 36 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0034 others(33): Show |
36 | HG01081.hp1 HG01169.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.487+286dupT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201607 | |||||||
chr18:70201607 | C | CAA | 30 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(27): Show |
30 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.487+285_487+286dup others(2): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201607 | |||||||
chr18:70201607 | C | CAAA | 10 | a0002c0001t0001g0095 a0002c0001t0001g0096 a0002c0001t0001g0098 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+284_487+286dup others(3): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201607 | |||||||
chr18:70201607 | CA | C | 24 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(21): Show |
24 | HG01168.hp2 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.487+286delT | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201607 | |||||||
chr18:70201607 | CAA | C | 8 | a0001c0006t0020g0120 a0001c0006t0021g0119 a0001c0011t0004g0151 others(5): Show |
8 | HG00099.hp2 HG00639.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+285_487+286del others(2): Show |
RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201607 | |||||||
chr18:70201616 | A | G | 1 | a0001c0021t0017g0131 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.487+278T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201616 | |||||||
chr18:70201674 | C | T | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.487+220G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201674 | |||||||
chr18:70201777 | A | G | 31 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(28): Show |
32 | HG00099.hp2 HG00639.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.487+117T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 4/48 | chr18 | 70201777 | |||||||
chr18:70202151 | T | C | 28 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(25): Show |
28 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.398-168A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202151 | |||||||
chr18:70202204 | T | G | 3 | a0001c0011t0004g0151 a0001c0011t0004g0152 a0002c0017t0002g0102 |
3 | HG00099.hp2 HG00639.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.398-221A>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202204 | |||||||
chr18:70202240 | G | A | 6 | a0001c0006t0001g0001 a0001c0006t0001g0122 a0001c0006t0001g0123 others(3): Show |
7 | HG01106.hp1 HG01168.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-257C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202240 | |||||||
chr18:70202290 | C | A | 5 | a0001c0005t0001g0141 a0001c0008t0008g0115 a0001c0008t0008g0116 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-307G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202290 | |||||||
chr18:70202297 | C | T | 10 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.398-314G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202297 | |||||||
chr18:70202351 | C | A | 5 | a0001c0005t0001g0109 a0001c0005t0001g0110 a0001c0005t0001g0111 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.398-368G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202351 | |||||||
chr18:70202427 | G | A | 4 | a0001c0008t0008g0115 a0001c0008t0008g0116 a0001c0008t0008g0117 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-444C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202427 | |||||||
chr18:70202598 | A | G | 26 | a0001c0002t0004g0108 a0001c0002t0004g0121 a0001c0002t0004g0153 others(23): Show |
27 | HG01106.hp1 HG01168.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-615T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202598 | |||||||
chr18:70202764 | T | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.398-781A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202764 | |||||||
chr18:70202967 | CT | C | 17 | a0001c0002t0004g0121 a0001c0006t0001g0001 a0001c0006t0001g0122 others(14): Show |
18 | HG01106.hp1 HG01168.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.398-985delA | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70202967 | |||||||
chr18:70203163 | T | C | 10 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.397+923A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203163 | |||||||
chr18:70203271 | C | A | 64 | a0002c0001t0001g0072 a0002c0001t0001g0073 a0002c0001t0001g0075 others(61): Show |
64 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.397+815G>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203271 | |||||||
chr18:70203295 | C | G | 2 | a0002c0003t0001g0047 a0002c0003t0001g0048 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.397+791G>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203295 | |||||||
chr18:70203347 | C | T | 29 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(26): Show |
29 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.397+739G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203347 | |||||||
chr18:70203463 | G | C | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.397+623C>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203463 | |||||||
chr18:70203473 | C | T | 1 | a0004c0026t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.397+613G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203473 | |||||||
chr18:70203591 | G | A | 3 | a0001c0009t0001g0039 a0001c0009t0001g0040 a0001c0009t0004g0142 |
3 | HG02735.hp2 HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.397+495C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203591 | |||||||
chr18:70203645 | A | G | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.397+441T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203645 | |||||||
chr18:70203661 | A | C | 2 | a0003c0004t0003g0002 a0003c0004t0003g0003 |
2 | HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.397+425T>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203661 | |||||||
chr18:70203740 | C | T | 1 | a0001c0022t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.397+346G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203740 | |||||||
chr18:70203988 | G | A | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.397+98C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203988 | |||||||
chr18:70203992 | G | A | 30 | a0001c0002t0001g0035 a0001c0002t0001g0139 a0001c0002t0002g0025 others(27): Show |
30 | HG01255.hp2 HG01346.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.397+94C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 3/48 | chr18 | 70203992 | |||||||
chr18:70204275 | A | G | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-12T>C | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/48 | chr18 | 70204275 | |||||||
chr18:70204297 | T | C | 2 | a0001c0009t0001g0039 a0001c0009t0001g0040 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.220-34A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/48 | chr18 | 70204297 | |||||||
chr18:70204524 | T | C | 6 | a0001c0007t0001g0145 a0001c0007t0001g0146 a0001c0007t0001g0147 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-261A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/48 | chr18 | 70204524 | |||||||
chr18:70204780 | T | C | 2 | a0001c0011t0004g0151 a0001c0011t0004g0152 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.219+348A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/48 | chr18 | 70204780 | |||||||
chr18:70204966 | T | C | 1 | a0001c0002t0004g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+162A>G | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 2/48 | chr18 | 70204966 | |||||||
chr18:70205318 | G | A | 1 | a0002c0003t0001g0154 | 1 | HG01169.hp1 | splice_region_variant&intron_variant | LOW | c.32-3C>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/48 | chr18 | 70205318 | |||||||
chr18:70205343 | T | A | 1 | a0001c0002t0002g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.32-28A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/48 | chr18 | 70205343 | |||||||
chr18:70205464 | T | A | 1 | a0001c0023t0014g0155 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.32-149A>T | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/48 | chr18 | 70205464 | |||||||
chr18:70205477 | C | T | 4 | a0002c0001t0005g0043 a0002c0001t0005g0044 a0002c0001t0024g0042 others(1): Show |
4 | HG00735.hp2 HG01361.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+151G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/48 | chr18 | 70205477 | |||||||
chr18:70205542 | C | T | 19 | a0001c0002t0001g0035 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
19 | HG01346.hp2 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+86G>A | RTTN | ENSG00000176225.15 | transcript | ENST00000640769.2 | protein_coding | 1/48 | chr18 | 70205542 |