Item | Value |
---|---|
geneid | 83593 |
ensemblid | ENSG00000266094.8 |
hgncid | 17609 |
symbol | RASSF5 |
name | Ras association domain family member 5 |
refseq_nuc | NM_182663.4 |
refseq_prot | NP_872604.1 |
ensembl_nuc | ENST00000579436.7 |
ensembl_prot | ENSP00000462099.1 |
mane_status | MANE Select |
chr | chr1 |
start | 206507531 |
end | 206589448 |
strand | + |
ver | v1.2 |
region | chr1:206507531-206589448 |
region5000 | chr1:206502531-206594448 |
regionname0 | RASSF5_chr1_206507531_206589448 |
regionname5000 | RASSF5_chr1_206502531_206594448 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 418 | 328 | 87 | 63 | 134 | 10 | 32 | 98 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0002 | 0/0 | 418 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0003 | 0/0 | 418 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0004 | 0/0 | 418 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0005 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0006 | 0/0 | 418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0007 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
a0008 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | MAMAS others(413): Show |
chr1 | 206502531 | 206594448 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1254 | 253 | 58 | 48 | 111 | 6 | 29 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0002 | 0/0 | 1254 | 42 | 13 | 6 | 21 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0003 | 1/0 | 1254 | 13 | 1 | 6 | 0 | 2 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0004 | 0/0 | 1254 | 12 | 12 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0007 | 0/0 | 1254 | 4 | 3 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0008 | 0/0 | 1254 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0010 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0001c0016 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0002c0005 | 0/0 | 1254 | 7 | 7 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0002c0013 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0003c0006 | 0/0 | 1254 | 4 | 0 | 0 | 4 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0004c0009 | 0/0 | 1254 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0005c0015 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0006c0014 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0007c0011 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 | ||
a0008c0012 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | ATGGC others(1249): Show |
chr1 | 206502531 | 206594448 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3799 | 76 | 10 | 23 | 32 | 1 | 9 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0002 | 0/0 | 3799 | 55 | 7 | 9 | 35 | 2 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0003 | 0/0 | 3799 | 57 | 10 | 10 | 25 | 2 | 10 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0004 | 0/0 | 3799 | 2 | 1 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0005 | 0/0 | 3799 | 7 | 3 | 1 | 1 | 1 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0006 | 0/0 | 3799 | 12 | 9 | 1 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0007 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0008 | 0/0 | 3799 | 10 | 0 | 0 | 10 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0009 | 0/0 | 3799 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0010 | 0/0 | 3799 | 6 | 0 | 0 | 3 | 0 | 3 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0011 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0012 | 0/0 | 3799 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0013 | 0/0 | 3799 | 3 | 2 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0014 | 0/0 | 3799 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0016 | 0/0 | 3799 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0017 | 0/0 | 3809 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3804): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0018 | 0/0 | 3799 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0019 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0021 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0025 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0029 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0001t0031 | 0/0 | 3799 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0001 | 0/0 | 3799 | 4 | 0 | 3 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0002 | 0/0 | 3799 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0003 | 0/0 | 3799 | 3 | 2 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0004 | 0/0 | 3799 | 20 | 1 | 1 | 16 | 2 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0009 | 0/0 | 3799 | 5 | 5 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0015 | 0/0 | 3799 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0020 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0022 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0026 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0002t0027 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0003t0001 | 1/0 | 3799 | 2 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0003t0002 | 0/0 | 3799 | 2 | 1 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0003t0005 | 0/0 | 3799 | 9 | 0 | 6 | 0 | 1 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0003 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0005 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0007 | 0/0 | 3799 | 6 | 6 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0013 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0024 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0004t0030 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0007t0002 | 0/0 | 3799 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0007t0011 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0007t0023 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0008t0005 | 0/0 | 3799 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0010t0003 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0001c0016t0002 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0002c0005t0001 | 0/0 | 3799 | 3 | 3 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0002c0005t0003 | 0/0 | 3799 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0002c0005t0007 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0002c0005t0028 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0002c0013t0004 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0003c0006t0001 | 0/0 | 3799 | 3 | 0 | 0 | 3 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0003c0006t0005 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0004c0009t0001 | 0/0 | 3799 | 2 | 0 | 0 | 0 | 0 | 2 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0005c0015t0001 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0006c0014t0001 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0007c0011t0006 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
a0008c0012t0002 | 0/0 | 3799 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | CTCTC others(3794): Show |
chr1 | 206502531 | 206594448 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0010g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0012g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0014g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0016g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0016g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0018g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0019g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0021g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0025g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0029g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0001t0031g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0015g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0020g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0022g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0026g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0002t0027g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0003t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0024g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0004t0030g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0007t0023g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0008t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0008t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0010t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0001c0016t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0005t0028g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0002c0013t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0003c0006t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0004c0009t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0004c0009t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0005c0015t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0006c0014t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0007c0011t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
a0008c0012t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0224 | EUR | GBR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0259 | EUR | GBR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00323 | hp1 | a0001 | c0003 | t0005 | g0239 | EUR | FIN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00323 | hp2 | a0001 | c0002 | t0004 | g0282 | EUR | FIN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00438 | hp2 | a0005 | c0015 | t0001 | g0256 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0167 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00609 | hp2 | a0001 | c0002 | t0027 | g0200 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00738 | hp1 | a0001 | c0003 | t0005 | g0234 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0236 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01069 | hp2 | a0006 | c0014 | t0001 | g0082 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0182 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01081 | hp1 | a0001 | c0003 | t0005 | g0233 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01081 | hp2 | a0001 | c0001 | t0021 | g0061 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01099 | hp1 | a0001 | c0003 | t0005 | g0235 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0035 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01109 | hp2 | a0001 | c0001 | t0013 | g0052 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01168 | hp1 | a0001 | c0003 | t0005 | g0219 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01169 | hp2 | a0001 | c0003 | t0005 | g0180 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01243 | hp1 | a0001 | c0007 | t0002 | g0221 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0316 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01346 | hp1 | a0001 | c0002 | t0020 | g0120 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0210 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0231 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0211 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0293 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0196 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0292 | EUR | IBS | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0232 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01884 | hp2 | a0001 | c0004 | t0007 | g0001 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0311 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01952 | hp2 | a0001 | c0008 | t0005 | g0108 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01978 | hp2 | a0001 | c0008 | t0005 | g0107 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02055 | hp1 | a0001 | c0002 | t0022 | g0312 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02056 | hp1 | a0003 | c0006 | t0001 | g0116 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02074 | hp1 | a0001 | c0002 | t0004 | g0111 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0170 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02132 | hp1 | a0001 | c0001 | t0010 | g0077 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0241 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0202 | EAS | CDX | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CDX | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02258 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02280 | hp1 | a0001 | c0004 | t0024 | g0023 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02451 | hp1 | a0002 | c0013 | t0004 | g0209 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02615 | hp2 | a0002 | c0005 | t0028 | g0208 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02622 | hp1 | a0001 | c0002 | t0009 | g0160 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02622 | hp2 | a0002 | c0005 | t0007 | g0189 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0074 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0306 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02717 | hp2 | a0001 | c0004 | t0013 | g0105 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02735 | hp2 | a0001 | c0003 | t0005 | g0230 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02809 | hp1 | a0001 | c0002 | t0009 | g0185 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02818 | hp1 | a0001 | c0004 | t0007 | g0106 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0056 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02895 | hp1 | a0002 | c0005 | t0001 | g0183 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02895 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02897 | hp2 | a0002 | c0005 | t0001 | g0184 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02922 | hp1 | a0001 | c0001 | t0029 | g0012 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02922 | hp2 | a0002 | c0005 | t0001 | g0188 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02965 | hp1 | a0001 | c0002 | t0015 | g0318 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02965 | hp2 | a0001 | c0004 | t0030 | g0046 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02970 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0313 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02976 | hp1 | a0001 | c0002 | t0026 | g0043 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0161 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03041 | hp1 | a0007 | c0011 | t0006 | g0310 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03041 | hp2 | a0001 | c0007 | t0002 | g0222 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0319 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03098 | hp2 | a0002 | c0005 | t0003 | g0186 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0118 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0117 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03209 | hp2 | a0001 | c0004 | t0003 | g0103 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03239 | hp2 | a0001 | c0001 | t0031 | g0228 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03453 | hp1 | a0001 | c0004 | t0006 | g0022 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03486 | hp1 | a0001 | c0007 | t0023 | g0223 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03486 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03490 | hp1 | a0004 | c0009 | t0001 | g0291 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03492 | hp2 | a0004 | c0009 | t0001 | g0045 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03516 | hp2 | a0001 | c0004 | t0005 | g0021 | AFR | ESN | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03654 | hp1 | a0001 | c0001 | t0010 | g0321 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03669 | hp1 | a0001 | c0001 | t0018 | g0285 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03688 | hp1 | a0001 | c0001 | t0010 | g0212 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0218 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03710 | hp1 | a0001 | c0003 | t0005 | g0060 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0309 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0177 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0002 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18906 | hp2 | a0002 | c0005 | t0003 | g0187 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18948 | hp1 | a0001 | c0001 | t0016 | g0301 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0092 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18954 | hp1 | a0001 | c0002 | t0004 | g0102 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0261 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0252 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18971 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18979 | hp2 | a0001 | c0001 | t0016 | g0300 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0098 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18981 | hp2 | a0001 | c0001 | t0010 | g0070 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18984 | hp1 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18985 | hp2 | a0001 | c0016 | t0002 | g0132 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18986 | hp1 | a0001 | c0010 | t0003 | g0265 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18986 | hp2 | a0003 | c0006 | t0001 | g0115 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18990 | hp1 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18993 | hp1 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18998 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18999 | hp2 | a0001 | c0002 | t0004 | g0217 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0168 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19004 | hp1 | a0003 | c0006 | t0001 | g0124 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19007 | hp1 | a0003 | c0006 | t0005 | g0114 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19007 | hp2 | a0001 | c0002 | t0004 | g0175 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0146 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19011 | hp2 | a0001 | c0002 | t0004 | g0174 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0198 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19030 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0053 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19067 | hp2 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0158 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0171 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19086 | hp1 | a0001 | c0002 | t0004 | g0169 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19086 | hp2 | a0001 | c0001 | t0017 | g0047 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19091 | hp1 | a0008 | c0012 | t0002 | g0190 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0181 | AFR | YRI | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20129 | hp1 | a0001 | c0002 | t0015 | g0243 | AFR | ASW | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20129 | hp2 | a0001 | c0004 | t0007 | g0104 | AFR | ASW | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0199 | SAS | GIH | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | GIH | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0002 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG02559 | hp2 | a0001 | c0002 | t0009 | g0242 | AFR | ACB | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG03471 | hp2 | a0001 | c0007 | t0011 | g0220 | AFR | MSL | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG06807 | hp1 | a0001 | c0004 | t0007 | g0001 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | USA | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0089 | REF | REF | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0240 | REF | REF | RASSF5_chr1_206502531_206594448 | RASSF5 | chr1 | 206502531 | 206594448 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206507760 | C | A | 1 | a0007 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.158C>A | p.Ala53Glu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 230/3799 | 158/1257 | 53/418 | chr1 | 206507760 | |||
chr1:206507789 | C | T | 1 | a0005 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.187C>T | p.Arg63Trp | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 259/3799 | 187/1257 | 63/418 | chr1 | 206507789 | |||
chr1:206507816 | C | T | 1 | a0006 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.214C>T | p.Pro72Ser | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 286/3799 | 214/1257 | 72/418 | chr1 | 206507816 | |||
chr1:206508050 | C | T | 1 | a0002 | 8 | HG02451.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
missense_variant | MODERATE | c.448C>T | p.Arg150Cys | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 520/3799 | 448/1257 | 150/418 | chr1 | 206508050 | |||
chr1:206538279 | G | A | 1 | a0003 | 4 | HG02056.hp1 NA18986.hp2 NA19004.hp1 others(1): Show |
missense_variant | MODERATE | c.565G>A | p.Val189Met | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 637/3799 | 565/1257 | 189/418 | chr1 | 206538279 | |||
chr1:206584439 | G | A | 1 | a0008 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.743G>A | p.Arg248Gln | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 815/3799 | 743/1257 | 248/418 | chr1 | 206584439 | |||
chr1:206584663 | C | T | 1 | a0004 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.967C>T | p.Arg323Trp | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 1039/3799 | 967/1257 | 323/418 | chr1 | 206584663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206507650 | A | C | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
332 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(329): Show |
synonymous_variant | LOW | c.48A>C | p.Leu16Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 120/3799 | 48/1257 | 16/418 | chr1 | 206507650 | |||
chr1:206507651 | T | C | 1 | a0001c0010 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.49T>C | p.Leu17Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 121/3799 | 49/1257 | 17/418 | chr1 | 206507651 | |||
chr1:206507689 | C | T | 1 | a0001c0016 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.87C>T | p.Ser29Ser | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 159/3799 | 87/1257 | 29/418 | chr1 | 206507689 | |||
chr1:206507990 | C | T | 1 | a0001c0004 | 12 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.388C>T | p.Leu130Leu | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/6 | 460/3799 | 388/1257 | 130/418 | chr1 | 206507990 | |||
chr1:206538179 | A | G | 1 | a0001c0007 | 4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
synonymous_variant | LOW | c.465A>G | p.Lys155Lys | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 537/3799 | 465/1257 | 155/418 | chr1 | 206538179 | |||
chr1:206538281 | G | A | 1 | a0001c0008 | 2 | HG01952.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.567G>A | p.Val189Val | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/6 | 639/3799 | 567/1257 | 189/418 | chr1 | 206538281 | |||
chr1:206584525 | C | A | 2 | a0001c0002 a0002c0013 |
43 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(40): Show |
synonymous_variant | LOW | c.829C>A | p.Arg277Arg | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/6 | 901/3799 | 829/1257 | 277/418 | chr1 | 206584525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206587021 | G | GTATTATT others(3): Show |
1 | a0001c0001t0017 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51_*60dupAATTATTA others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 61 | INFO_REALIGN_3_PRIME | chr1 | 206587021 | |||||
chr1:206587142 | C | T | 9 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0029 others(6): Show |
77 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*164C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 164 | chr1 | 206587142 | ||||||
chr1:206587144 | A | G | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(42): Show |
243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*166A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 166 | chr1 | 206587144 | ||||||
chr1:206587162 | C | T | 1 | a0001c0001t0031 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 184 | chr1 | 206587162 | ||||||
chr1:206587304 | C | G | 1 | a0001c0001t0021 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 326 | chr1 | 206587304 | ||||||
chr1:206587354 | A | T | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(18): Show |
159 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 376 | chr1 | 206587354 | ||||||
chr1:206587362 | C | T | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
206 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*384C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 384 | chr1 | 206587362 | ||||||
chr1:206587416 | T | C | 2 | a0001c0001t0011 a0001c0007t0011 |
4 | HG03139.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*438T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 438 | chr1 | 206587416 | ||||||
chr1:206587489 | C | G | 1 | a0001c0002t0027 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 511 | chr1 | 206587489 | ||||||
chr1:206587719 | G | A | 2 | a0001c0002t0015 a0001c0002t0022 |
3 | HG02055.hp1 HG02965.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*741G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 741 | chr1 | 206587719 | ||||||
chr1:206588034 | C | T | 1 | a0001c0002t0020 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1056 | chr1 | 206588034 | ||||||
chr1:206588099 | G | A | 4 | a0001c0001t0007 a0001c0001t0012 a0001c0004t0007 others(1): Show |
14 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1121G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1121 | chr1 | 206588099 | ||||||
chr1:206588120 | G | A | 1 | a0001c0007t0023 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1142 | chr1 | 206588120 | ||||||
chr1:206588460 | G | C | 1 | a0002c0005t0028 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1482G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1482 | chr1 | 206588460 | ||||||
chr1:206588592 | A | G | 1 | a0001c0001t0016 | 2 | NA18948.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1614A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1614 | chr1 | 206588592 | ||||||
chr1:206588606 | T | C | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0013 others(13): Show |
89 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1628T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1628 | chr1 | 206588606 | ||||||
chr1:206588623 | A | G | 1 | a0001c0001t0012 | 4 | HG02647.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1645A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1645 | chr1 | 206588623 | ||||||
chr1:206588709 | C | T | 1 | a0001c0001t0019 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1731C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1731 | chr1 | 206588709 | ||||||
chr1:206588829 | A | C | 2 | a0001c0001t0025 a0001c0004t0024 |
2 | HG02280.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1851A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1851 | chr1 | 206588829 | ||||||
chr1:206588863 | T | G | 1 | a0001c0002t0022 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1885T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1885 | chr1 | 206588863 | ||||||
chr1:206588948 | A | T | 2 | a0001c0004t0024 a0001c0004t0030 |
2 | HG02280.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1970A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 1970 | chr1 | 206588948 | ||||||
chr1:206588993 | A | G | 1 | a0001c0001t0018 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2015 | chr1 | 206588993 | ||||||
chr1:206589123 | C | T | 5 | a0001c0001t0006 a0001c0002t0006 a0001c0004t0006 others(2): Show |
16 | HG01257.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2145C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2145 | chr1 | 206589123 | ||||||
chr1:206589328 | C | T | 1 | a0001c0001t0008 | 10 | HG00558.hp2 HG02129.hp1 NA18971.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2350C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2350 | chr1 | 206589328 | ||||||
chr1:206589343 | G | A | 4 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0025 others(1): Show |
11 | HG01109.hp2 HG02109.hp1 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2365G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2365 | chr1 | 206589343 | ||||||
chr1:206589352 | C | T | 8 | a0001c0001t0004 a0001c0001t0029 a0001c0002t0004 others(5): Show |
29 | HG00099.hp2 HG00323.hp2 HG01070.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2374C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 6/6 | 2374 | chr1 | 206589352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:206508171 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.457+112G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508171 | |||||||
chr1:206508322 | C | CCA | 66 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(63): Show |
72 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.457+295_457+296dup others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508322 | C | CCACA | 21 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0039 others(18): Show |
21 | HG01109.hp1 HG02055.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.457+293_457+296dup others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508322 | C | CCACACAC others(3): Show |
2 | a0001c0001t0002g0024 a0001c0001t0003g0025 |
2 | HG03139.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.457+287_457+296dup others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508322 | C | CCACACAC others(5): Show |
3 | a0001c0004t0005g0021 a0001c0004t0006g0022 a0001c0004t0024g0023 |
3 | HG02280.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+285_457+296dup others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508322 | CCA | C | 14 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0314 others(11): Show |
15 | HG00597.hp1 HG00621.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+295_457+296del others(2): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508322 | CCACA | C | 7 | a0001c0001t0001g0323 a0001c0001t0002g0322 a0001c0001t0002g0326 others(4): Show |
7 | HG01361.hp2 HG02818.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+293_457+296del others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206508322 | ||||||
chr1:206508383 | G | T | 1 | a0001c0001t0006g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.457+324G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508383 | |||||||
chr1:206508423 | C | T | 2 | a0001c0001t0001g0017 a0001c0008t0005g0107 |
3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.457+364C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508423 | |||||||
chr1:206508697 | C | G | 10 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(7): Show |
13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.457+638C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508697 | |||||||
chr1:206508705 | A | G | 69 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0101 others(66): Show |
73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.457+646A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508705 | |||||||
chr1:206508857 | G | A | 3 | a0001c0001t0002g0097 a0001c0001t0003g0096 a0001c0001t0003g0250 |
3 | HG02135.hp2 NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.457+798G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206508857 | |||||||
chr1:206509015 | T | G | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+956T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509015 | |||||||
chr1:206509625 | T | C | 83 | a0001c0001t0001g0027 a0001c0001t0001g0112 a0001c0001t0001g0122 others(80): Show |
88 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.457+1566T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509625 | |||||||
chr1:206509639 | A | T | 1 | a0001c0001t0002g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.457+1580A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509639 | |||||||
chr1:206509726 | CT | C | 155 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(152): Show |
164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+1679delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206509726 | ||||||
chr1:206509758 | G | A | 12 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(9): Show |
15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1699G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509758 | |||||||
chr1:206509762 | G | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(112): Show |
119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+1703G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509762 | |||||||
chr1:206509788 | G | C | 1 | a0001c0004t0030g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.457+1729G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509788 | |||||||
chr1:206509836 | C | T | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+1777C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509836 | |||||||
chr1:206509893 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457+1834G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206509893 | |||||||
chr1:206510060 | A | C | 1 | a0001c0001t0003g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.457+2001A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510060 | |||||||
chr1:206510251 | G | T | 12 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0244 others(9): Show |
12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+2192G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510251 | |||||||
chr1:206510358 | CTCTG | C | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+2301_457+2304d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206510358 | ||||||
chr1:206510390 | A | G | 159 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(156): Show |
168 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.457+2331A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510390 | |||||||
chr1:206510434 | A | C | 1 | a0001c0004t0007g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.457+2375A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510434 | |||||||
chr1:206510560 | C | T | 1 | a0001c0002t0001g0304 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.457+2501C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510560 | |||||||
chr1:206510644 | A | G | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+2585A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510644 | |||||||
chr1:206510768 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0003g0109 a0001c0001t0003g0110 others(1): Show |
4 | HG02071.hp1 HG02074.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+2709T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510768 | |||||||
chr1:206510785 | C | A | 1 | a0001c0001t0005g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.457+2726C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206510785 | |||||||
chr1:206511364 | C | T | 1 | a0001c0001t0003g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.457+3305C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511364 | |||||||
chr1:206511464 | C | G | 1 | a0001c0004t0030g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.457+3405C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511464 | |||||||
chr1:206511644 | A | C | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(164): Show |
176 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.457+3585A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511644 | |||||||
chr1:206511645 | A | T | 167 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(164): Show |
176 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.457+3586A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511645 | |||||||
chr1:206511687 | C | G | 1 | a0001c0001t0002g0302 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.457+3628C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511687 | |||||||
chr1:206511689 | A | G | 10 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(7): Show |
13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.457+3630A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511689 | |||||||
chr1:206511794 | C | T | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.457+3735C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511794 | |||||||
chr1:206511815 | C | CCACTTTC others(2): Show |
2 | a0001c0001t0003g0010 a0001c0001t0004g0176 |
3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.457+3769_457+3777d others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206511815 | ||||||
chr1:206511818 | C | T | 1 | a0001c0001t0010g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.457+3759C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511818 | |||||||
chr1:206511852 | C | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+3793C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206511852 | |||||||
chr1:206512069 | G | A | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+4010G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512069 | |||||||
chr1:206512091 | G | A | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+4032G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512091 | |||||||
chr1:206512294 | T | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(322): Show |
343 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.457+4235T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512294 | |||||||
chr1:206512299 | C | T | 1 | a0001c0001t0010g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.457+4240C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512299 | |||||||
chr1:206512309 | C | A | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+4250C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512309 | |||||||
chr1:206512371 | G | A | 2 | a0001c0003t0005g0180 a0001c0003t0005g0219 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.457+4312G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512371 | |||||||
chr1:206512396 | C | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(112): Show |
119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+4337C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512396 | |||||||
chr1:206512564 | C | T | 13 | a0001c0001t0001g0172 a0001c0001t0001g0308 a0001c0001t0003g0010 others(10): Show |
14 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.457+4505C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512564 | |||||||
chr1:206512819 | C | A | 3 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0004t0024g0023 |
3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.457+4760C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512819 | |||||||
chr1:206512978 | G | A | 4 | a0001c0001t0002g0113 a0003c0006t0001g0115 a0003c0006t0001g0116 others(1): Show |
4 | HG00438.hp1 HG02056.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+4919G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206512978 | |||||||
chr1:206513027 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0002g0119 a0001c0001t0006g0123 others(4): Show |
7 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+4968G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513027 | |||||||
chr1:206513211 | C | A | 1 | a0001c0002t0009g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.457+5152C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513211 | |||||||
chr1:206513789 | G | C | 3 | a0001c0001t0002g0119 a0001c0001t0011g0117 a0001c0001t0011g0118 |
3 | HG02109.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.457+5730G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513789 | |||||||
chr1:206513910 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.457+5851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513910 | |||||||
chr1:206513930 | C | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(38): Show |
44 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.457+5871C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206513930 | |||||||
chr1:206514232 | C | T | 1 | a0001c0004t0006g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.457+6173C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514232 | |||||||
chr1:206514547 | G | A | 4 | a0001c0001t0005g0042 a0001c0001t0007g0248 a0001c0001t0007g0249 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+6488G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514547 | |||||||
chr1:206514553 | T | C | 22 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0002g0305 others(19): Show |
27 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.457+6494T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514553 | |||||||
chr1:206514603 | T | C | 313 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(310): Show |
331 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.457+6544T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514603 | |||||||
chr1:206514720 | A | T | 1 | a0001c0001t0002g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.457+6661A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206514720 | |||||||
chr1:206515032 | G | A | 12 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0244 others(9): Show |
12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.457+6973G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515032 | |||||||
chr1:206515083 | G | T | 1 | a0001c0001t0003g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.457+7024G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515083 | |||||||
chr1:206515235 | C | T | 4 | a0001c0001t0005g0042 a0001c0001t0007g0248 a0001c0001t0007g0249 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+7176C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515235 | |||||||
chr1:206515253 | G | C | 1 | a0001c0002t0002g0320 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.457+7194G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515253 | |||||||
chr1:206515418 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.457+7359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515418 | |||||||
chr1:206515626 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0003g0005 a0001c0001t0003g0094 |
4 | HG01993.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+7567C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515626 | |||||||
chr1:206515895 | C | A | 1 | a0001c0002t0002g0320 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.457+7836C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206515895 | |||||||
chr1:206516441 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.457+8382A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516441 | |||||||
chr1:206516462 | C | CT | 6 | a0001c0001t0001g0017 a0001c0001t0002g0119 a0001c0001t0005g0048 others(3): Show |
7 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+8415dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206516462 | ||||||
chr1:206516658 | C | T | 22 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0002g0305 others(19): Show |
27 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.457+8599C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516658 | |||||||
chr1:206516810 | C | T | 2 | a0001c0001t0001g0017 a0001c0008t0005g0107 |
3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.457+8751C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516810 | |||||||
chr1:206516811 | G | A | 1 | a0001c0002t0004g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.457+8752G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516811 | |||||||
chr1:206516953 | C | T | 149 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(146): Show |
158 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.457+8894C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516953 | |||||||
chr1:206516994 | G | A | 2 | a0002c0005t0001g0183 a0002c0005t0001g0184 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.457+8935G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206516994 | |||||||
chr1:206517293 | G | A | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.457+9234G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517293 | |||||||
chr1:206517405 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+9346G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517405 | |||||||
chr1:206517413 | A | C | 12 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(9): Show |
15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+9354A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517413 | |||||||
chr1:206517436 | C | T | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+9377C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517436 | |||||||
chr1:206517450 | T | C | 155 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(152): Show |
164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+9391T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517450 | |||||||
chr1:206517524 | G | A | 12 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(9): Show |
15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+9465G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517524 | |||||||
chr1:206517532 | T | A | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+9473T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517532 | |||||||
chr1:206517881 | C | A | 1 | a0001c0001t0021g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.457+9822C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517881 | |||||||
chr1:206517910 | A | C | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+9851A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206517910 | |||||||
chr1:206518019 | G | A | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+9960G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518019 | |||||||
chr1:206518172 | C | G | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+10113C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518172 | |||||||
chr1:206518454 | C | T | 1 | a0001c0002t0015g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.457+10395C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518454 | |||||||
chr1:206518744 | G | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(112): Show |
119 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.457+10685G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518744 | |||||||
chr1:206518834 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.457+10775G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518834 | |||||||
chr1:206518950 | T | G | 1 | a0001c0002t0015g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457+10891T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206518950 | |||||||
chr1:206519135 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0019g0092 |
2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.457+11076C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519135 | |||||||
chr1:206519169 | G | A | 12 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(9): Show |
15 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+11110G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519169 | |||||||
chr1:206519201 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0004g0176 |
3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.457+11142T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519201 | |||||||
chr1:206519258 | T | C | 4 | a0001c0001t0005g0042 a0001c0001t0007g0248 a0001c0001t0007g0249 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+11199T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519258 | |||||||
chr1:206519300 | T | G | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(175): Show |
187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.457+11241T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519300 | |||||||
chr1:206519440 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | NA18984.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.457+11381C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519440 | |||||||
chr1:206519493 | G | C | 1 | a0001c0002t0009g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.457+11434G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519493 | |||||||
chr1:206519568 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.457+11509C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519568 | |||||||
chr1:206519826 | C | G | 175 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(172): Show |
184 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.457+11767C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206519826 | |||||||
chr1:206520333 | G | C | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+12274G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520333 | |||||||
chr1:206520337 | T | C | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+12278T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520337 | |||||||
chr1:206520410 | A | C | 197 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(194): Show |
207 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.457+12351A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520410 | |||||||
chr1:206520435 | C | T | 5 | a0001c0001t0001g0299 a0001c0001t0002g0322 a0001c0001t0003g0309 others(2): Show |
5 | HG01361.hp2 HG01993.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+12376C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520435 | |||||||
chr1:206520452 | G | T | 1 | a0001c0002t0004g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.457+12393G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520452 | |||||||
chr1:206520481 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.457+12422C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520481 | |||||||
chr1:206520531 | C | G | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.457+12472C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520531 | |||||||
chr1:206520545 | T | C | 178 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(175): Show |
187 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.457+12486T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520545 | |||||||
chr1:206520563 | C | T | 1 | a0001c0001t0003g0006 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.457+12504C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520563 | |||||||
chr1:206520564 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.457+12505G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520564 | |||||||
chr1:206520594 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(319): Show |
340 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(337): Show |
intron_variant | MODIFIER | c.457+12535A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520594 | |||||||
chr1:206520606 | C | CA | 150 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(147): Show |
155 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.457+12563dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206520606 | ||||||
chr1:206520606 | C | CAAAA | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+12560_457+1256 others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206520606 | ||||||
chr1:206520642 | G | A | 116 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(113): Show |
120 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.457+12583G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520642 | |||||||
chr1:206520838 | A | C | 159 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(156): Show |
164 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+12779A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206520838 | |||||||
chr1:206521056 | T | A | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+12997T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521056 | |||||||
chr1:206521178 | G | A | 8 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.457+13119G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521178 | |||||||
chr1:206521337 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+13278G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521337 | |||||||
chr1:206521346 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.457+13287T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521346 | |||||||
chr1:206521366 | A | T | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+13307A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521366 | |||||||
chr1:206521567 | T | C | 3 | a0001c0001t0002g0119 a0001c0001t0011g0117 a0001c0001t0011g0118 |
3 | HG02109.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.457+13508T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521567 | |||||||
chr1:206521576 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18953.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.457+13517A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521576 | |||||||
chr1:206521847 | G | T | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.457+13788G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521847 | |||||||
chr1:206521902 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0016t0002g0132 |
3 | NA18960.hp2 NA18982.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.457+13843G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521902 | |||||||
chr1:206521927 | G | A | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+13868G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206521927 | |||||||
chr1:206522184 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.457+14125T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522184 | |||||||
chr1:206522251 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14192G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522251 | |||||||
chr1:206522254 | CAAATGAA others(60): Show |
C | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14196_457+1426 others(71): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522254 | |||||||
chr1:206522325 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14266T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522325 | |||||||
chr1:206522331 | C | G | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14272C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522331 | |||||||
chr1:206522333 | C | A | 50 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0147 others(47): Show |
54 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.457+14274C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522333 | |||||||
chr1:206522333 | C | G | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14274C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522333 | |||||||
chr1:206522337 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.457+14278G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522337 | |||||||
chr1:206522398 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0002g0305 a0001c0001t0003g0025 others(18): Show |
25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.457+14339G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522398 | |||||||
chr1:206522433 | A | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.457+14374A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522433 | |||||||
chr1:206522482 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+14423G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522482 | |||||||
chr1:206522608 | A | T | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.457+14549A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522608 | |||||||
chr1:206522614 | G | A | 2 | a0001c0001t0001g0251 a0001c0002t0004g0252 |
2 | HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.457+14555G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522614 | |||||||
chr1:206522800 | T | A | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+14741T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522800 | |||||||
chr1:206522857 | AAAAATGA others(10): Show |
A | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14803_457+1481 others(21): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206522857 | ||||||
chr1:206522879 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14820A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522879 | |||||||
chr1:206522881 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14822T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522881 | |||||||
chr1:206522886 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14827A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522886 | |||||||
chr1:206522889 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14830G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522889 | |||||||
chr1:206522891 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14832T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522891 | |||||||
chr1:206522892 | T | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14833T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522892 | |||||||
chr1:206522894 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14835A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522894 | |||||||
chr1:206522896 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14837C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522896 | |||||||
chr1:206522897 | T | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14838T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522897 | |||||||
chr1:206522898 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14839A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522898 | |||||||
chr1:206522903 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14844A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522903 | |||||||
chr1:206522904 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14845A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522904 | |||||||
chr1:206522906 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.457+14847A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522906 | |||||||
chr1:206522910 | C | T | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+14851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206522910 | |||||||
chr1:206523102 | C | G | 2 | a0004c0009t0001g0045 a0004c0009t0001g0291 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.457+15043C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523102 | |||||||
chr1:206523405 | AATATTAT | A | 119 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(116): Show |
123 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.458-14749_458-1474 others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523405 | ||||||
chr1:206523423 | T | A | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14749T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523423 | |||||||
chr1:206523430 | A | T | 4 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0006g0018 others(1): Show |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-14742A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523430 | |||||||
chr1:206523441 | A | G | 2 | a0001c0003t0005g0180 a0001c0003t0005g0219 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.458-14731A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523441 | |||||||
chr1:206523461 | A | AATATATT others(28): Show |
1 | a0001c0001t0001g0062 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.458-14696_458-1466 others(39): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523461 | ||||||
chr1:206523480 | ATATAATA others(9): Show |
A | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14691_458-1467 others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523480 | |||||||
chr1:206523481 | TATA | T | 8 | a0001c0001t0001g0011 a0001c0001t0002g0225 a0001c0001t0002g0226 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-14687_458-1468 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523481 | ||||||
chr1:206523482 | ATAATATT others(13): Show |
A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14688_458-1466 others(24): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523482 | ||||||
chr1:206523484 | AATATTAT others(16): Show |
A | 231 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(228): Show |
240 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.458-14653_458-1463 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523484 | ||||||
chr1:206523485 | ATATTATA others(19): Show |
A | 8 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-14683_458-1465 others(30): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523485 | ||||||
chr1:206523505 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14667T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523505 | |||||||
chr1:206523513 | ATATATTA others(14): Show |
A | 1 | a0001c0016t0002g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14653_458-1463 others(25): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523513 | ||||||
chr1:206523527 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14645T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523527 | |||||||
chr1:206523543 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14629T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523543 | |||||||
chr1:206523600 | T | G | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-14572T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523600 | |||||||
chr1:206523612 | A | ATATATAA others(31): Show |
23 | a0001c0001t0001g0027 a0001c0001t0001g0112 a0001c0001t0001g0122 others(20): Show |
24 | HG00597.hp2 HG00609.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.458-14527_458-1449 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523612 | ||||||
chr1:206523612 | ATATATAA others(31): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.458-14527_458-1449 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523612 | ||||||
chr1:206523634 | A | ATTATATA others(30): Show |
1 | a0001c0001t0010g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.458-14537_458-1450 others(41): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523634 | ||||||
chr1:206523635 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14537T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523635 | |||||||
chr1:206523649 | T | TTTATATA others(30): Show |
5 | a0001c0001t0002g0113 a0003c0006t0001g0115 a0003c0006t0001g0116 others(2): Show |
5 | HG00438.hp1 HG02056.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(41): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523649 | ||||||
chr1:206523657 | A | AAATATAT others(31): Show |
5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(42): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523657 | ||||||
chr1:206523657 | A | AAATATAT others(121): Show |
4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14490_458-1448 others(132): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523657 | ||||||
chr1:206523657 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.458-14515A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523657 | |||||||
chr1:206523680 | TA | T | 4 | a0001c0001t0001g0057 a0001c0001t0004g0247 a0001c0001t0009g0056 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14489delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523680 | ||||||
chr1:206523705 | A | C | 1 | a0001c0001t0003g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.458-14467A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523705 | |||||||
chr1:206523723 | T | TTA | 231 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(228): Show |
240 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.458-14443_458-1444 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523723 | ||||||
chr1:206523729 | A | ATTATATA others(8): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0062 others(15): Show |
19 | HG00423.hp2 HG00558.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.458-14440_458-1442 others(19): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523729 | ||||||
chr1:206523735 | T | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0002g0305 others(23): Show |
31 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.458-14437T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523735 | |||||||
chr1:206523806 | CAATATAT others(16): Show |
C | 1 | a0001c0003t0005g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-14349_458-1432 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523806 | ||||||
chr1:206523821 | A | ATTATATA others(32): Show |
9 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0165 others(6): Show |
9 | HG02074.hp2 HG02083.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-14342_458-1430 others(43): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523821 | ||||||
chr1:206523839 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14333T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523839 | |||||||
chr1:206523849 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.458-14323A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523849 | |||||||
chr1:206523878 | T | A | 1 | a0001c0001t0003g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458-14294T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523878 | |||||||
chr1:206523893 | T | C | 1 | a0001c0002t0020g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.458-14279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523893 | |||||||
chr1:206523900 | T | TATATATT others(27): Show |
2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-14217_458-1418 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523900 | ||||||
chr1:206523918 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.458-14254T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523918 | |||||||
chr1:206523925 | A | G | 1 | a0001c0001t0010g0177 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.458-14247A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523925 | |||||||
chr1:206523949 | TAA | T | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-14222_458-1422 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523949 | |||||||
chr1:206523951 | A | T | 1 | a0001c0016t0002g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14221A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523951 | |||||||
chr1:206523952 | T | A | 1 | a0001c0016t0002g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14220T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523952 | |||||||
chr1:206523953 | A | T | 1 | a0001c0016t0002g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.458-14219A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523953 | |||||||
chr1:206523955 | A | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14217A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523955 | |||||||
chr1:206523960 | C | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14212C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523960 | |||||||
chr1:206523969 | A | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14203A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523969 | |||||||
chr1:206523972 | T | C | 5 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0005t0001g0188 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-14200T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523972 | |||||||
chr1:206523985 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-14187A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523985 | |||||||
chr1:206523988 | T | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14184T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523988 | |||||||
chr1:206523988 | T | TATATACC others(61): Show |
2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14184_458-1418 others(72): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523988 | |||||||
chr1:206523988 | T | TGTATACC others(27): Show |
1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.458-14179_458-1417 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206523988 | ||||||
chr1:206523993 | AT | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14178delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523993 | |||||||
chr1:206523994 | T | C | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14178T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206523994 | |||||||
chr1:206524003 | G | A | 6 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-14169G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524003 | |||||||
chr1:206524016 | A | C | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14156A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524016 | |||||||
chr1:206524028 | C | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14144C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524028 | |||||||
chr1:206524050 | A | C | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-14122A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524050 | |||||||
chr1:206524056 | G | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14116G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524056 | |||||||
chr1:206524062 | A | C | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14110A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524062 | |||||||
chr1:206524065 | TATATA | T | 71 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0101 others(68): Show |
75 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.458-14101_458-1409 others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524065 | ||||||
chr1:206524085 | TAA | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14086_458-1408 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524085 | |||||||
chr1:206524091 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14081G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524091 | |||||||
chr1:206524092 | T | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14080T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524092 | |||||||
chr1:206524099 | TATATA | T | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-14067_458-1406 others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524099 | ||||||
chr1:206524102 | A | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14070A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524102 | |||||||
chr1:206524110 | T | C | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14062T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524110 | |||||||
chr1:206524112 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-14060T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524112 | |||||||
chr1:206524119 | T | TAA | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-14053_458-1405 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524119 | |||||||
chr1:206524140 | T | A | 1 | a0002c0005t0007g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.458-14032T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524140 | |||||||
chr1:206524208 | T | C | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13964T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524208 | |||||||
chr1:206524210 | C | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13962C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524210 | |||||||
chr1:206524221 | A | ATATAGAT others(27): Show |
9 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-13889_458-1385 others(38): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524221 | ||||||
chr1:206524221 | A | ATATAGAT others(61): Show |
7 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(4): Show |
10 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-13931_458-1393 others(72): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524221 | ||||||
chr1:206524221 | A | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13951A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524221 | |||||||
chr1:206524242 | C | T | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13930C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524242 | |||||||
chr1:206524244 | T | C | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13928T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524244 | |||||||
chr1:206524246 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13926T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524246 | |||||||
chr1:206524250 | A | ATATAATA others(59): Show |
1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.458-13918_458-1391 others(70): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524250 | ||||||
chr1:206524260 | G | T | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13912G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524260 | |||||||
chr1:206524283 | T | C | 2 | a0001c0001t0002g0054 a0008c0012t0002g0190 |
2 | NA18951.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.458-13889T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524283 | |||||||
chr1:206524317 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 |
3 | NA18979.hp1 NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.458-13855C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524317 | |||||||
chr1:206524404 | A | G | 1 | a0001c0001t0008g0158 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.458-13768A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524404 | |||||||
chr1:206524443 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13729A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524443 | |||||||
chr1:206524456 | A | ATT | 6 | a0001c0001t0002g0159 a0001c0001t0005g0164 a0001c0001t0012g0009 others(3): Show |
8 | HG02622.hp1 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-13715_458-1371 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524456 | ||||||
chr1:206524457 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13715T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524457 | |||||||
chr1:206524466 | T | A | 1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13706T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524466 | |||||||
chr1:206524551 | C | CATAAATA others(52): Show |
1 | a0001c0001t0002g0135 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.458-13618_458-1361 others(63): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524551 | ||||||
chr1:206524558 | A | AATATATT others(18): Show |
1 | a0001c0001t0001g0290 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.458-13604_458-1358 others(29): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(52): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0255 a0001c0001t0001g0294 others(2): Show |
6 | HG00438.hp2 NA18947.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-13588_458-1358 others(63): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(77): Show |
1 | a0001c0001t0001g0257 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.458-13588_458-1358 others(88): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(25): Show |
3 | a0001c0001t0001g0057 a0001c0001t0002g0258 a0001c0001t0009g0056 |
3 | HG02630.hp1 HG02886.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.458-13579_458-1354 others(36): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(50): Show |
181 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0031 others(178): Show |
187 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.458-13560_458-1350 others(61): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(75): Show |
3 | a0001c0001t0001g0101 a0001c0001t0002g0289 a0001c0001t0003g0100 |
3 | NA18956.hp1 NA18960.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.458-13604_458-1352 others(86): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(107): Show |
5 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(2): Show |
5 | HG00099.hp2 HG00642.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-13504_458-1350 others(118): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(43): Show |
1 | a0001c0001t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.458-13580_458-1357 others(54): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524558 | A | AATATATT others(48): Show |
1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13598_458-1359 others(59): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524558 | ||||||
chr1:206524587 | T | A | 4 | a0001c0007t0002g0221 a0001c0007t0002g0222 a0001c0007t0011g0220 others(1): Show |
4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13585T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524587 | |||||||
chr1:206524589 | T | A | 4 | a0001c0007t0002g0221 a0001c0007t0002g0222 a0001c0007t0011g0220 others(1): Show |
4 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13583T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524589 | |||||||
chr1:206524589 | T | TTATATAT others(50): Show |
3 | a0001c0001t0012g0319 a0001c0004t0007g0001 a0001c0004t0013g0105 |
4 | HG02258.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-13548_458-1354 others(61): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | ||||||
chr1:206524589 | T | TTATATAT others(114): Show |
2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-13548_458-1354 others(125): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | ||||||
chr1:206524589 | T | TTATATAT others(75): Show |
2 | a0004c0009t0001g0045 a0004c0009t0001g0291 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.458-13504_458-1350 others(86): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | ||||||
chr1:206524589 | T | TTATGTAT others(68): Show |
4 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13580_458-1357 others(79): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524589 | ||||||
chr1:206524614 | A | ATATATAT | 7 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0004t0003g0103 others(4): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.458-13554_458-1354 others(11): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524614 | ||||||
chr1:206524614 | A | ATATATAT others(82): Show |
1 | a0001c0002t0004g0102 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.458-13504_458-1350 others(93): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524614 | ||||||
chr1:206524615 | T | G | 4 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13557T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524615 | |||||||
chr1:206524637 | A | AAATATAT others(16): Show |
3 | a0001c0001t0012g0319 a0001c0004t0007g0001 a0001c0004t0013g0105 |
4 | HG02258.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-13518_458-1349 others(27): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | ||||||
chr1:206524637 | A | AAATATAT others(98): Show |
1 | a0001c0004t0007g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.458-13504_458-1350 others(109): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | ||||||
chr1:206524637 | A | AAATATAT others(66): Show |
2 | a0001c0004t0007g0001 a0001c0004t0007g0104 |
3 | HG01884.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(77): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | ||||||
chr1:206524637 | A | AAATATAT others(114): Show |
2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(125): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | ||||||
chr1:206524637 | A | AAATATAT others(116): Show |
3 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0004t0024g0023 |
3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.458-13523_458-1352 others(127): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524637 | ||||||
chr1:206524640 | T | G | 4 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13532T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524640 | |||||||
chr1:206524650 | A | G | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13522A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524650 | |||||||
chr1:206524654 | T | A | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13518T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524654 | |||||||
chr1:206524657 | G | A | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13515G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524657 | |||||||
chr1:206524662 | A | AAAGATAT others(82): Show |
1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-13510_458-1350 others(93): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524662 | |||||||
chr1:206524662 | A | ATATATAT others(57): Show |
2 | a0001c0001t0005g0048 a0001c0001t0017g0047 |
2 | NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.458-13478_458-1347 others(68): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524662 | ||||||
chr1:206524662 | A | ATATATAT others(89): Show |
2 | a0001c0001t0001g0017 a0001c0008t0005g0107 |
3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.458-13478_458-1347 others(100): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206524662 | ||||||
chr1:206524662 | A | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13510A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524662 | |||||||
chr1:206524675 | A | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-13497A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524675 | |||||||
chr1:206524850 | C | T | 2 | a0001c0001t0003g0211 a0001c0001t0005g0210 |
2 | HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.458-13322C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524850 | |||||||
chr1:206524916 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0002g0305 a0001c0001t0003g0025 others(18): Show |
25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.458-13256G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524916 | |||||||
chr1:206524964 | A | T | 2 | a0001c0001t0001g0017 a0001c0008t0005g0107 |
3 | HG01256.hp1 HG01258.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.458-13208A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524964 | |||||||
chr1:206524990 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13182T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524990 | |||||||
chr1:206524991 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13181C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524991 | |||||||
chr1:206524993 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-13179T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206524993 | |||||||
chr1:206525015 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0002g0157 |
3 | NA18942.hp2 NA18947.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.458-13157C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525015 | |||||||
chr1:206525016 | A | G | 243 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(240): Show |
255 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.458-13156A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525016 | |||||||
chr1:206525106 | C | T | 5 | a0001c0001t0002g0059 a0001c0007t0002g0221 a0001c0007t0002g0222 others(2): Show |
5 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-13066C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525106 | |||||||
chr1:206525156 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0013g0002 others(6): Show |
10 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-13016T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525156 | |||||||
chr1:206525220 | C | T | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12952C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525220 | |||||||
chr1:206525278 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0003g0196 others(2): Show |
5 | HG01433.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-12894G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525278 | |||||||
chr1:206525386 | C | A | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12786C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525386 | |||||||
chr1:206525404 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.458-12768G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525404 | |||||||
chr1:206525408 | G | T | 21 | a0001c0001t0001g0017 a0001c0001t0002g0305 a0001c0001t0003g0025 others(18): Show |
25 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.458-12764G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525408 | |||||||
chr1:206525608 | AAAAACAA others(3): Show |
A | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.458-12549_458-1254 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206525608 | ||||||
chr1:206525758 | G | T | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-12414G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525758 | |||||||
chr1:206525936 | C | G | 1 | a0001c0002t0009g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.458-12236C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206525936 | |||||||
chr1:206526136 | C | G | 10 | a0001c0001t0005g0207 a0001c0002t0003g0035 a0002c0005t0001g0183 others(7): Show |
10 | HG01109.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-12036C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526136 | |||||||
chr1:206526140 | C | T | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-12032C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526140 | |||||||
chr1:206526269 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0002g0059 a0001c0007t0002g0221 a0001c0007t0002g0222 others(2): Show |
5 | HG01243.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-11886_458-1187 others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(3): Show |
42 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0055 others(39): Show |
45 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.458-11888_458-1187 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0003g0041 a0001c0001t0006g0018 a0001c0001t0006g0311 |
4 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-11890_458-1187 others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(7): Show |
14 | a0001c0001t0001g0064 a0001c0001t0001g0073 a0001c0001t0001g0197 others(11): Show |
17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.458-11892_458-1187 others(18): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(9): Show |
59 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0150 others(56): Show |
61 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.458-11894_458-1187 others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(11): Show |
105 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(102): Show |
110 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.458-11896_458-1187 others(22): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(13): Show |
29 | a0001c0001t0001g0031 a0001c0001t0001g0136 a0001c0001t0001g0262 others(26): Show |
29 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.458-11898_458-1187 others(24): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(15): Show |
14 | a0001c0001t0001g0127 a0001c0001t0002g0126 a0001c0001t0003g0100 others(11): Show |
14 | HG01952.hp2 HG02056.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.458-11900_458-1187 others(26): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(17): Show |
7 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0296 others(4): Show |
7 | HG00609.hp1 HG01175.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-11902_458-1187 others(28): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(19): Show |
10 | a0001c0001t0002g0113 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
11 | HG00438.hp1 HG02071.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-11879_458-1187 others(30): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(21): Show |
1 | a0001c0001t0006g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.458-11879_458-1187 others(32): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526269 | A | AGTGTGTG others(23): Show |
2 | a0001c0001t0001g0027 a0001c0001t0006g0026 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.458-11879_458-1187 others(34): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206526269 | ||||||
chr1:206526293 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-11879_458-1187 others(23): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526293 | |||||||
chr1:206526295 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.458-11877G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526295 | |||||||
chr1:206526303 | G | A | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-11869G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526303 | |||||||
chr1:206526352 | C | T | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0131 |
3 | NA18984.hp2 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.458-11820C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526352 | |||||||
chr1:206526438 | A | G | 27 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0002g0305 others(24): Show |
32 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.458-11734A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526438 | |||||||
chr1:206526744 | G | A | 1 | a0001c0002t0004g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.458-11428G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526744 | |||||||
chr1:206526834 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.458-11338C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526834 | |||||||
chr1:206526870 | G | A | 2 | a0001c0002t0001g0121 a0001c0002t0020g0120 |
2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.458-11302G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526870 | |||||||
chr1:206526933 | G | A | 13 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(10): Show |
13 | NA18612.hp2 NA18747.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-11239G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206526933 | |||||||
chr1:206527127 | T | C | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-11045T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527127 | |||||||
chr1:206527131 | A | C | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-11041A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527131 | |||||||
chr1:206527267 | C | G | 2 | a0001c0001t0001g0122 a0001c0001t0006g0123 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.458-10905C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527267 | |||||||
chr1:206527284 | C | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-10888C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527284 | |||||||
chr1:206527366 | G | T | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-10806G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527366 | |||||||
chr1:206527456 | G | A | 45 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0147 others(42): Show |
47 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.458-10716G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527456 | |||||||
chr1:206527491 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.458-10681C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527491 | |||||||
chr1:206527610 | C | T | 2 | a0001c0002t0001g0121 a0001c0002t0020g0120 |
2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.458-10562C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527610 | |||||||
chr1:206527678 | T | C | 7 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(4): Show |
8 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-10494T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527678 | |||||||
chr1:206527833 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0006g0026 a0001c0001t0006g0028 |
3 | HG02572.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.458-10339C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206527833 | |||||||
chr1:206528139 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.458-10033G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528139 | |||||||
chr1:206528196 | C | A | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.458-9976C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528196 | |||||||
chr1:206528248 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.458-9924A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528248 | |||||||
chr1:206528402 | G | T | 5 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0005t0001g0188 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-9770G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528402 | |||||||
chr1:206528580 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0006g0033 a0001c0001t0006g0034 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-9592G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528580 | |||||||
chr1:206528669 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.458-9503G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528669 | |||||||
chr1:206528715 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.458-9457G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528715 | |||||||
chr1:206528866 | C | T | 3 | a0001c0001t0002g0135 a0001c0001t0002g0156 a0001c0001t0008g0158 |
3 | NA18959.hp2 NA18967.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.458-9306C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528866 | |||||||
chr1:206528905 | A | G | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458-9267A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528905 | |||||||
chr1:206528960 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-9212G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206528960 | |||||||
chr1:206529122 | T | C | 27 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0002g0305 others(24): Show |
32 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.458-9050T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529122 | |||||||
chr1:206529275 | G | A | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-8897G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529275 | |||||||
chr1:206529294 | C | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-8878C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529294 | |||||||
chr1:206529323 | G | A | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-8849G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529323 | |||||||
chr1:206529334 | C | T | 1 | a0001c0002t0004g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.458-8838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529334 | |||||||
chr1:206529336 | C | T | 1 | a0001c0002t0003g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-8836C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529336 | |||||||
chr1:206529386 | G | A | 46 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0147 others(43): Show |
48 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.458-8786G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529386 | |||||||
chr1:206529424 | G | T | 8 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-8748G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529424 | |||||||
chr1:206529444 | C | G | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-8728C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529444 | |||||||
chr1:206529479 | C | T | 1 | a0001c0001t0004g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458-8693C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529479 | |||||||
chr1:206529544 | C | T | 12 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0244 others(9): Show |
12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-8628C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529544 | |||||||
chr1:206529578 | G | A | 1 | a0001c0003t0005g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.458-8594G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529578 | |||||||
chr1:206529677 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.458-8495G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529677 | |||||||
chr1:206529699 | C | T | 1 | a0001c0004t0003g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.458-8473C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529699 | |||||||
chr1:206529765 | C | CA | 216 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(213): Show |
227 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.458-8397dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206529765 | ||||||
chr1:206529765 | C | CAA | 6 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(3): Show |
7 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-8398_458-8397d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206529765 | ||||||
chr1:206529786 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0003g0005 a0001c0001t0003g0094 |
4 | HG01993.hp2 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-8386G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529786 | |||||||
chr1:206529840 | G | T | 1 | a0001c0002t0003g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-8332G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206529840 | |||||||
chr1:206530069 | C | T | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-8103C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530069 | |||||||
chr1:206530070 | G | A | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.458-8102G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530070 | |||||||
chr1:206530152 | T | A | 243 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(240): Show |
255 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.458-8020T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530152 | |||||||
chr1:206530155 | CT | C | 10 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(7): Show |
13 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-8016delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530155 | |||||||
chr1:206530203 | T | G | 1 | a0002c0005t0007g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.458-7969T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530203 | |||||||
chr1:206530344 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.458-7828C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530344 | |||||||
chr1:206530440 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-7732T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530440 | |||||||
chr1:206530627 | A | G | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(111): Show |
118 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.458-7545A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530627 | |||||||
chr1:206530780 | C | G | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-7392C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530780 | |||||||
chr1:206530796 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0003g0109 a0001c0001t0003g0110 others(3): Show |
6 | HG00597.hp2 HG00609.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-7376G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530796 | |||||||
chr1:206530949 | C | G | 1 | a0001c0001t0009g0051 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.458-7223C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206530949 | |||||||
chr1:206531169 | G | A | 12 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0244 others(9): Show |
12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-7003G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531169 | |||||||
chr1:206531354 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-6818C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531354 | |||||||
chr1:206531364 | G | A | 1 | a0001c0001t0002g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.458-6808G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531364 | |||||||
chr1:206531369 | G | A | 1 | a0001c0001t0010g0321 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.458-6803G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531369 | |||||||
chr1:206531477 | A | G | 12 | a0001c0001t0002g0246 a0001c0001t0003g0012 a0001c0001t0003g0244 others(9): Show |
12 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-6695A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531477 | |||||||
chr1:206531539 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.458-6633G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531539 | |||||||
chr1:206531606 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0005g0048 a0001c0001t0017g0047 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-6566C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531606 | |||||||
chr1:206531715 | T | C | 46 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0147 others(43): Show |
48 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.458-6457T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531715 | |||||||
chr1:206531813 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-6359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531813 | |||||||
chr1:206531872 | C | T | 1 | a0001c0002t0015g0318 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.458-6300C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531872 | |||||||
chr1:206531873 | T | TAA | 8 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0319 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-6291_458-6290d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206531873 | ||||||
chr1:206531883 | T | A | 283 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.458-6289T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531883 | |||||||
chr1:206531883 | T | TA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0003g0324 others(15): Show |
20 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.458-6286dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206531883 | ||||||
chr1:206531907 | C | T | 2 | a0001c0001t0011g0117 a0001c0001t0011g0118 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.458-6265C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531907 | |||||||
chr1:206531913 | A | G | 5 | a0001c0001t0001g0323 a0001c0001t0003g0324 a0001c0001t0003g0325 others(2): Show |
6 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-6259A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531913 | |||||||
chr1:206531922 | G | A | 1 | a0001c0001t0004g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.458-6250G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206531922 | |||||||
chr1:206532058 | G | GA | 192 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(189): Show |
205 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.458-6104dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206532058 | ||||||
chr1:206532058 | G | GAA | 9 | a0001c0001t0001g0017 a0001c0001t0002g0225 a0001c0001t0005g0048 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-6105_458-6104d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206532058 | ||||||
chr1:206532276 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(285): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.458-5896A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532276 | |||||||
chr1:206532298 | A | G | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-5874A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532298 | |||||||
chr1:206532343 | C | T | 10 | a0001c0001t0001g0031 a0001c0001t0002g0322 a0001c0001t0003g0309 others(7): Show |
11 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-5829C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532343 | |||||||
chr1:206532611 | C | T | 4 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0001t0012g0009 others(1): Show |
5 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-5561C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532611 | |||||||
chr1:206532758 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.458-5414G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532758 | |||||||
chr1:206532906 | A | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0003g0324 others(14): Show |
18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.458-5266A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206532906 | |||||||
chr1:206533086 | A | G | 192 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0027 others(189): Show |
201 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.458-5086A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533086 | |||||||
chr1:206533256 | G | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0323 a0001c0001t0003g0324 others(7): Show |
11 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.458-4916G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533256 | |||||||
chr1:206533278 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0003g0038 a0001c0002t0003g0037 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-4894G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533278 | |||||||
chr1:206533332 | A | C | 3 | a0001c0001t0003g0155 a0001c0001t0008g0137 a0001c0001t0008g0154 |
3 | HG02129.hp1 HG02523.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.458-4840A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533332 | |||||||
chr1:206533728 | C | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-4444C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206533728 | |||||||
chr1:206534049 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-4123C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534049 | |||||||
chr1:206534425 | G | C | 1 | a0001c0001t0002g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.458-3747G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534425 | |||||||
chr1:206534560 | C | T | 1 | a0001c0001t0019g0092 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.458-3612C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534560 | |||||||
chr1:206534721 | T | A | 8 | a0001c0001t0001g0039 a0001c0001t0003g0038 a0001c0001t0011g0216 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-3451T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534721 | |||||||
chr1:206534787 | G | C | 2 | a0001c0007t0002g0221 a0001c0007t0011g0220 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.458-3385G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534787 | |||||||
chr1:206534855 | G | T | 1 | a0001c0002t0026g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.458-3317G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206534855 | |||||||
chr1:206535154 | G | A | 3 | a0001c0001t0001g0275 a0004c0009t0001g0045 a0004c0009t0001g0291 |
3 | HG00741.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.458-3018G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535154 | |||||||
chr1:206535382 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.458-2790T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535382 | |||||||
chr1:206535392 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
88 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.458-2780T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535392 | |||||||
chr1:206535530 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.458-2642G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535530 | |||||||
chr1:206535582 | A | G | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2590A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535582 | |||||||
chr1:206535686 | T | G | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.458-2486T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535686 | |||||||
chr1:206535703 | C | CTG | 3 | a0001c0001t0003g0309 a0001c0004t0003g0103 a0001c0004t0030g0046 |
3 | HG02965.hp2 HG03209.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.458-2458_458-2457d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535703 | ||||||
chr1:206535703 | C | G | 1 | a0001c0001t0017g0047 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458-2469C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535703 | |||||||
chr1:206535705 | G | C | 1 | a0001c0001t0017g0047 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.458-2467G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535705 | |||||||
chr1:206535712 | TGTG | T | 122 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(119): Show |
126 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.458-2456_458-2454d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535712 | ||||||
chr1:206535714 | TG | T | 61 | a0001c0001t0001g0057 a0001c0001t0001g0136 a0001c0001t0001g0138 others(58): Show |
66 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.458-2456delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535714 | ||||||
chr1:206535715 | G | GT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0050 others(45): Show |
51 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.458-2457_458-2456i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535715 | |||||||
chr1:206535715 | GGT | G | 7 | a0001c0001t0002g0059 a0001c0003t0001g0237 a0001c0003t0005g0060 others(4): Show |
7 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-2429_458-2428d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535715 | ||||||
chr1:206535715 | GGTGT | G | 69 | a0001c0001t0001g0027 a0001c0001t0001g0112 a0001c0001t0001g0122 others(66): Show |
72 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.458-2431_458-2428d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206535715 | ||||||
chr1:206535716 | G | T | 13 | a0001c0001t0001g0031 a0001c0001t0001g0323 a0001c0001t0003g0324 others(10): Show |
15 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-2456G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535716 | |||||||
chr1:206535717 | T | G | 13 | a0001c0001t0001g0031 a0001c0001t0001g0323 a0001c0001t0003g0324 others(10): Show |
15 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-2455T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535717 | |||||||
chr1:206535718 | GT | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0050 others(103): Show |
114 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.458-2453delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535718 | |||||||
chr1:206535720 | GT | G | 122 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0017 others(119): Show |
126 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.458-2451delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535720 | |||||||
chr1:206535743 | T | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0262 a0001c0001t0003g0006 others(6): Show |
11 | HG00642.hp1 HG01346.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-2429T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535743 | |||||||
chr1:206535745 | A | T | 7 | a0001c0001t0001g0031 a0001c0001t0006g0018 a0001c0001t0006g0033 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-2427A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535745 | |||||||
chr1:206535747 | A | T | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2425A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535747 | |||||||
chr1:206535749 | A | T | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2423A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535749 | |||||||
chr1:206535751 | A | T | 2 | a0001c0004t0005g0021 a0001c0004t0006g0022 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.458-2421A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535751 | |||||||
chr1:206535779 | A | G | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.458-2393A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535779 | |||||||
chr1:206535979 | C | T | 3 | a0001c0001t0002g0305 a0001c0001t0003g0025 a0001c0004t0024g0023 |
3 | HG02280.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.458-2193C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206535979 | |||||||
chr1:206536063 | G | A | 1 | a0001c0001t0003g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.458-2109G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536063 | |||||||
chr1:206536100 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0003g0038 a0001c0002t0003g0037 others(3): Show |
6 | HG02055.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-2072G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536100 | |||||||
chr1:206536144 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.458-2028C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536144 | |||||||
chr1:206536206 | T | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0050 others(113): Show |
121 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.458-1966T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536206 | |||||||
chr1:206536238 | A | G | 1 | a0001c0001t0003g0325 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.458-1934A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536238 | |||||||
chr1:206536333 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.458-1839A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536333 | |||||||
chr1:206536549 | AG | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0005g0048 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-1617delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr1 | 206536549 | ||||||
chr1:206536694 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.458-1478A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536694 | |||||||
chr1:206536783 | C | A | 1 | a0001c0002t0009g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.458-1389C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536783 | |||||||
chr1:206536901 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0003g0205 |
2 | NA18983.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.458-1271A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206536901 | |||||||
chr1:206537012 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0006g0018 a0001c0001t0006g0033 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-1160A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537012 | |||||||
chr1:206537024 | C | T | 1 | a0001c0002t0015g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.458-1148C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537024 | |||||||
chr1:206537062 | C | T | 1 | a0001c0002t0022g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.458-1110C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537062 | |||||||
chr1:206537285 | C | G | 1 | a0001c0001t0031g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.458-887C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537285 | |||||||
chr1:206537547 | G | A | 1 | a0001c0001t0006g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.458-625G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537547 | |||||||
chr1:206537696 | G | A | 7 | a0001c0001t0005g0207 a0001c0001t0013g0002 a0001c0001t0013g0052 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-476G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537696 | |||||||
chr1:206537771 | T | G | 7 | a0001c0001t0005g0207 a0001c0001t0013g0002 a0001c0001t0013g0052 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-401T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537771 | |||||||
chr1:206537807 | T | G | 7 | a0001c0001t0001g0031 a0001c0001t0006g0018 a0001c0001t0006g0033 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-365T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537807 | |||||||
chr1:206537817 | T | C | 21 | a0001c0001t0002g0159 a0001c0001t0002g0326 a0001c0001t0003g0012 others(18): Show |
24 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.458-355T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537817 | |||||||
chr1:206537893 | T | C | 10 | a0001c0001t0005g0207 a0001c0001t0009g0030 a0001c0001t0009g0051 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537893 | |||||||
chr1:206537960 | CA | C | 7 | a0001c0001t0005g0207 a0001c0001t0013g0002 a0001c0001t0013g0052 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-211delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537960 | |||||||
chr1:206537974 | G | C | 1 | a0001c0001t0003g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.458-198G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206537974 | |||||||
chr1:206538069 | C | G | 7 | a0001c0001t0005g0207 a0001c0001t0013g0002 a0001c0001t0013g0052 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-103C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 1/5 | chr1 | 206538069 | |||||||
chr1:206538583 | A | G | 17 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(14): Show |
20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+290A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538583 | |||||||
chr1:206538649 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0065 others(3): Show |
7 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+356G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538649 | |||||||
chr1:206538710 | C | G | 2 | a0001c0001t0011g0117 a0001c0001t0011g0118 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+417C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538710 | |||||||
chr1:206538750 | C | T | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+457C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538750 | |||||||
chr1:206538784 | A | G | 17 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(14): Show |
20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+491A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538784 | |||||||
chr1:206538793 | G | A | 1 | a0001c0002t0004g0169 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.579+500G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538793 | |||||||
chr1:206538795 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0006g0018 a0001c0001t0006g0033 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+502A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538795 | |||||||
chr1:206538989 | G | A | 17 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(14): Show |
20 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+696G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206538989 | |||||||
chr1:206539214 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(183): Show |
197 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.579+921A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539214 | |||||||
chr1:206539275 | T | C | 1 | a0001c0001t0019g0092 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.579+982T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539275 | |||||||
chr1:206539501 | C | T | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.579+1208C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539501 | |||||||
chr1:206539549 | A | G | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+1256A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539549 | |||||||
chr1:206539623 | C | T | 3 | a0001c0002t0003g0037 a0001c0002t0006g0036 a0001c0002t0009g0185 |
3 | HG02723.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.579+1330C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206539623 | |||||||
chr1:206540171 | G | T | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.579+1878G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540171 | |||||||
chr1:206540226 | G | C | 2 | a0001c0001t0003g0128 a0001c0001t0003g0179 |
2 | HG00597.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.579+1933G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540226 | |||||||
chr1:206540361 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579+2068A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540361 | |||||||
chr1:206540479 | C | T | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+2186C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540479 | |||||||
chr1:206540588 | A | G | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579+2295A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540588 | |||||||
chr1:206540635 | C | G | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+2342C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540635 | |||||||
chr1:206540759 | G | C | 27 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(24): Show |
30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2466G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540759 | |||||||
chr1:206540898 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(183): Show |
197 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.579+2605T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540898 | |||||||
chr1:206540901 | T | A | 27 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(24): Show |
30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2608T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540901 | |||||||
chr1:206540938 | A | G | 27 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(24): Show |
30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2645A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206540938 | |||||||
chr1:206541082 | T | A | 27 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(24): Show |
30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+2789T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541082 | |||||||
chr1:206541183 | C | T | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+2890C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541183 | |||||||
chr1:206541191 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(198): Show |
213 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.579+2898G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541191 | |||||||
chr1:206541462 | G | A | 1 | a0001c0004t0003g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579+3169G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541462 | |||||||
chr1:206541489 | C | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(197): Show |
212 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(209): Show |
intron_variant | MODIFIER | c.579+3196C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541489 | |||||||
chr1:206541513 | C | T | 24 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(21): Show |
27 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+3220C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541513 | |||||||
chr1:206541516 | T | A | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+3223T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541516 | |||||||
chr1:206541679 | A | G | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3386A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541679 | |||||||
chr1:206541708 | T | C | 3 | a0001c0001t0002g0326 a0001c0002t0015g0243 a0001c0002t0022g0312 |
3 | HG02055.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.579+3415T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541708 | |||||||
chr1:206541806 | C | T | 2 | a0002c0005t0007g0189 a0002c0005t0028g0208 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+3513C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541806 | |||||||
chr1:206541857 | G | A | 15 | a0001c0001t0003g0088 a0001c0001t0003g0191 a0001c0001t0003g0192 others(12): Show |
16 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+3564G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541857 | |||||||
chr1:206541895 | C | T | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3602C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541895 | |||||||
chr1:206541928 | A | G | 3 | a0001c0001t0001g0290 a0001c0002t0001g0283 a0001c0002t0001g0304 |
3 | HG01952.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.579+3635A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541928 | |||||||
chr1:206541949 | A | C | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+3656A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206541949 | |||||||
chr1:206542021 | G | A | 14 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(11): Show |
17 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+3728G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542021 | |||||||
chr1:206542298 | A | G | 1 | a0001c0007t0002g0221 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.579+4005A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542298 | |||||||
chr1:206542387 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(227): Show |
245 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.579+4094G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542387 | |||||||
chr1:206542401 | C | T | 8 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0001t0007g0248 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+4108C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542401 | |||||||
chr1:206542463 | T | C | 2 | a0002c0005t0007g0189 a0002c0005t0028g0208 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+4170T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542463 | |||||||
chr1:206542465 | C | G | 3 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0181 |
3 | HG02896.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.579+4172C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542465 | |||||||
chr1:206542470 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.579+4177G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542470 | |||||||
chr1:206542518 | C | G | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+4225C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542518 | |||||||
chr1:206542522 | A | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(200): Show |
215 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.579+4229A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542522 | |||||||
chr1:206542648 | G | A | 7 | a0001c0001t0005g0207 a0001c0001t0013g0002 a0001c0001t0013g0052 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+4355G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542648 | |||||||
chr1:206542875 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+4582T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542875 | |||||||
chr1:206542986 | A | G | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+4693A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206542986 | |||||||
chr1:206543138 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.579+4845C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543138 | |||||||
chr1:206543221 | T | TAAA | 12 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0178 others(9): Show |
13 | HG01256.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+4942_579+4944d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | ||||||
chr1:206543221 | T | TAAAA | 182 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(179): Show |
193 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.579+4941_579+4944d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | ||||||
chr1:206543221 | T | TAAAAA | 9 | a0001c0001t0001g0065 a0001c0001t0001g0314 a0001c0001t0002g0024 others(6): Show |
9 | HG01175.hp2 HG01981.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+4940_579+4944d others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | ||||||
chr1:206543221 | T | TAAAAAA | 21 | a0001c0001t0003g0012 a0001c0001t0003g0244 a0001c0001t0003g0245 others(18): Show |
24 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.579+4939_579+4944d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | ||||||
chr1:206543221 | TA | T | 6 | a0001c0001t0002g0020 a0001c0001t0002g0322 a0001c0001t0003g0058 others(3): Show |
6 | HG00099.hp1 HG01069.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+4944delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543221 | ||||||
chr1:206543450 | C | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(224): Show |
242 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(239): Show |
intron_variant | MODIFIER | c.579+5157C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543450 | |||||||
chr1:206543565 | A | ATG | 7 | a0001c0001t0001g0262 a0001c0001t0002g0289 a0001c0001t0009g0030 others(4): Show |
7 | HG00642.hp1 HG00741.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+5298_579+5299d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543565 | ATG | A | 3 | a0001c0001t0002g0276 a0001c0001t0005g0048 a0001c0001t0017g0047 |
3 | HG00423.hp1 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.579+5298_579+5299d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543565 | ATGTG | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(203): Show |
221 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.579+5296_579+5299d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543565 | ATGTGTG | A | 18 | a0001c0001t0002g0326 a0001c0001t0003g0012 a0001c0001t0003g0244 others(15): Show |
18 | HG01952.hp2 HG01978.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+5294_579+5299d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543565 | ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0010g0212 a0001c0002t0003g0037 a0001c0002t0006g0036 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5292_579+5299d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543565 | ATGTGTGT others(3): Show |
A | 1 | a0001c0002t0022g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+5290_579+5299d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206543565 | ||||||
chr1:206543572 | T | C | 2 | a0002c0005t0007g0189 a0002c0005t0028g0208 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+5279T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543572 | |||||||
chr1:206543658 | G | T | 4 | a0001c0001t0002g0322 a0001c0001t0003g0058 a0001c0001t0005g0224 others(1): Show |
4 | HG00099.hp1 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5365G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543658 | |||||||
chr1:206543663 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0002g0162 |
2 | NA18747.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.579+5370C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543663 | |||||||
chr1:206543739 | T | C | 1 | a0002c0005t0001g0188 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.579+5446T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543739 | |||||||
chr1:206543806 | T | G | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+5513T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543806 | |||||||
chr1:206543884 | G | T | 1 | a0001c0004t0006g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.579+5591G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543884 | |||||||
chr1:206543968 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0006g0026 |
2 | HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579+5675G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206543968 | |||||||
chr1:206544039 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.579+5746A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544039 | |||||||
chr1:206544232 | G | A | 4 | a0001c0001t0001g0266 a0001c0001t0002g0113 a0001c0001t0002g0302 others(1): Show |
4 | HG00438.hp1 NA18959.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5939G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544232 | |||||||
chr1:206544234 | GGCTC | G | 3 | a0001c0002t0003g0037 a0001c0002t0006g0036 a0001c0002t0009g0185 |
3 | HG02723.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.579+5942_579+5945d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544234 | |||||||
chr1:206544318 | C | G | 19 | a0001c0001t0001g0031 a0001c0001t0005g0207 a0001c0001t0006g0018 others(16): Show |
20 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+6025C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544318 | |||||||
chr1:206544330 | T | G | 40 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0172 others(37): Show |
44 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.579+6037T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544330 | |||||||
chr1:206544385 | C | T | 15 | a0001c0001t0003g0012 a0001c0001t0003g0025 a0001c0001t0003g0244 others(12): Show |
18 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+6092C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544385 | |||||||
chr1:206544432 | A | G | 1 | a0001c0001t0010g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579+6139A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544432 | |||||||
chr1:206544656 | G | GC | 41 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0063 others(38): Show |
43 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.579+6365dupC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206544656 | ||||||
chr1:206544670 | A | T | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+6377A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544670 | |||||||
chr1:206544791 | G | A | 12 | a0001c0001t0002g0326 a0001c0001t0006g0018 a0001c0001t0006g0033 others(9): Show |
13 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+6498G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544791 | |||||||
chr1:206544813 | C | T | 8 | a0001c0001t0005g0048 a0001c0001t0009g0030 a0001c0001t0009g0051 others(5): Show |
8 | HG01952.hp2 HG01978.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6520C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544813 | |||||||
chr1:206544815 | T | C | 13 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0005g0207 others(10): Show |
14 | HG01109.hp1 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+6522T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544815 | |||||||
chr1:206544850 | C | A | 1 | a0001c0001t0012g0009 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579+6557C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544850 | |||||||
chr1:206544894 | G | GA | 8 | a0001c0001t0001g0290 a0001c0001t0009g0030 a0001c0001t0009g0051 others(5): Show |
8 | HG01109.hp2 HG01952.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6613dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206544894 | ||||||
chr1:206544895 | A | G | 1 | a0001c0002t0022g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+6602A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206544895 | |||||||
chr1:206545024 | G | A | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.579+6731G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545024 | |||||||
chr1:206545344 | TG | T | 4 | a0001c0004t0003g0103 a0001c0004t0030g0046 a0002c0005t0003g0186 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7052delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545344 | |||||||
chr1:206545345 | GT | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(151): Show |
166 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.579+7072delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | ||||||
chr1:206545345 | GTT | G | 131 | a0001c0001t0001g0027 a0001c0001t0001g0073 a0001c0001t0001g0090 others(128): Show |
135 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.579+7071_579+7072d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | ||||||
chr1:206545345 | GTTT | G | 17 | a0001c0001t0002g0119 a0001c0001t0003g0012 a0001c0001t0003g0245 others(14): Show |
18 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+7070_579+7072d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545345 | ||||||
chr1:206545348 | T | G | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0002c0005t0007g0189 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7055T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545348 | |||||||
chr1:206545352 | T | G | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.579+7059T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545352 | |||||||
chr1:206545356 | T | G | 4 | a0001c0004t0003g0103 a0001c0004t0030g0046 a0002c0005t0003g0186 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+7063T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545356 | |||||||
chr1:206545487 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0007g0032 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.579+7194G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545487 | |||||||
chr1:206545516 | GT | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(222): Show |
237 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.579+7230delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545516 | ||||||
chr1:206545524 | A | G | 32 | a0001c0001t0002g0119 a0001c0001t0003g0012 a0001c0001t0003g0245 others(29): Show |
34 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.579+7231A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545524 | |||||||
chr1:206545687 | C | A | 2 | a0002c0005t0007g0189 a0002c0005t0028g0208 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.579+7394C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545687 | |||||||
chr1:206545693 | T | C | 6 | a0001c0001t0001g0076 a0001c0001t0001g0296 a0001c0001t0002g0141 others(3): Show |
6 | HG01358.hp2 HG02083.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+7400T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545693 | |||||||
chr1:206545953 | A | AT | 10 | a0001c0001t0002g0119 a0001c0001t0002g0289 a0001c0001t0003g0213 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+7677dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545953 | ||||||
chr1:206545953 | AT | A | 27 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(24): Show |
28 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.579+7677delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206545953 | ||||||
chr1:206545979 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0260 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.579+7686C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206545979 | |||||||
chr1:206546089 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0005g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.579+7824_579+7833d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT | A | 4 | a0001c0001t0001g0031 a0001c0001t0007g0032 a0001c0004t0007g0001 others(1): Show |
7 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+7827_579+7833d others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(3): Show |
A | 32 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0081 others(29): Show |
33 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.579+7824_579+7833d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(4): Show |
A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(142): Show |
153 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.579+7823_579+7833d others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(5): Show |
A | 19 | a0001c0001t0001g0055 a0001c0001t0001g0068 a0001c0001t0001g0251 others(16): Show |
19 | HG00099.hp1 HG00738.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.579+7822_579+7833d others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+7821_579+7833d others(15): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0029g0012 |
3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+7820_579+7833d others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0003g0270 a0001c0001t0009g0030 a0001c0001t0009g0051 others(2): Show |
5 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+7819_579+7833d others(17): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(9): Show |
A | 15 | a0001c0001t0001g0290 a0001c0001t0002g0054 a0001c0001t0002g0133 others(12): Show |
15 | HG00323.hp2 HG01070.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.579+7818_579+7833d others(18): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(10): Show |
A | 46 | a0001c0001t0001g0076 a0001c0001t0001g0266 a0001c0001t0001g0280 others(43): Show |
48 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.579+7817_579+7833d others(19): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(11): Show |
A | 5 | a0001c0001t0001g0062 a0001c0001t0002g0119 a0001c0001t0006g0018 others(2): Show |
6 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+7816_579+7833d others(20): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546089 | ATTTTTTT others(12): Show |
A | 15 | a0001c0001t0002g0059 a0001c0001t0006g0033 a0001c0001t0006g0034 others(12): Show |
16 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+7815_579+7833d others(21): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206546089 | ||||||
chr1:206546124 | T | G | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+7831T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546124 | |||||||
chr1:206546125 | T | G | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.579+7832T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546125 | |||||||
chr1:206546126 | T | G | 23 | a0001c0001t0001g0027 a0001c0001t0002g0019 a0001c0001t0002g0020 others(20): Show |
24 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.579+7833T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546126 | |||||||
chr1:206546222 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+7929C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546222 | |||||||
chr1:206546223 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.579+7930T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546223 | |||||||
chr1:206546490 | C | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(297): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.579+8197C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546490 | |||||||
chr1:206546585 | G | A | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.579+8292G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546585 | |||||||
chr1:206546648 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(217): Show |
231 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.579+8355C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546648 | |||||||
chr1:206546689 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0260 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.579+8396C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546689 | |||||||
chr1:206546690 | A | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8397A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546690 | |||||||
chr1:206546795 | A | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0002g0292 |
3 | HG01515.hp2 HG01517.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.579+8502A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546795 | |||||||
chr1:206546856 | C | A | 198 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.579+8563C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546856 | |||||||
chr1:206546879 | G | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(297): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.579+8586G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546879 | |||||||
chr1:206546897 | G | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.579+8604G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206546897 | |||||||
chr1:206547216 | C | T | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8923C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547216 | |||||||
chr1:206547224 | C | T | 63 | a0001c0001t0001g0076 a0001c0001t0001g0178 a0001c0001t0001g0266 others(60): Show |
65 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.579+8931C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547224 | |||||||
chr1:206547264 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.579+8971G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547264 | |||||||
chr1:206547286 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.579+8993T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547286 | |||||||
chr1:206547437 | G | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(212): Show |
226 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.579+9144G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547437 | |||||||
chr1:206547458 | C | T | 10 | a0001c0001t0005g0207 a0001c0001t0011g0216 a0001c0001t0012g0009 others(7): Show |
11 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+9165C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547458 | |||||||
chr1:206547547 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.579+9254T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547547 | |||||||
chr1:206547891 | C | T | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.579+9598C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206547891 | |||||||
chr1:206548037 | T | G | 5 | a0001c0001t0002g0059 a0001c0004t0003g0103 a0001c0004t0030g0046 others(2): Show |
5 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+9744T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548037 | |||||||
chr1:206548051 | T | G | 32 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0138 others(29): Show |
32 | HG01261.hp1 HG02055.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.579+9758T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548051 | |||||||
chr1:206548164 | T | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0029g0012 |
3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+9871T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548164 | |||||||
chr1:206548404 | C | G | 1 | a0001c0001t0006g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.579+10111C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548404 | |||||||
chr1:206548502 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(196): Show |
209 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.579+10209G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548502 | |||||||
chr1:206548522 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+10229C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548522 | |||||||
chr1:206548647 | A | G | 1 | a0001c0001t0003g0229 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.579+10354A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548647 | |||||||
chr1:206548706 | G | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0029g0012 |
3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+10413G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548706 | |||||||
chr1:206548738 | C | G | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.579+10445C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548738 | |||||||
chr1:206548803 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0009g0030 others(4): Show |
7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10510G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548803 | |||||||
chr1:206548846 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+10553C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548846 | |||||||
chr1:206548874 | ATTTTGTT others(3): Show |
A | 1 | a0001c0001t0001g0011 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579+10582_579+1059 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548874 | |||||||
chr1:206548884 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0009g0030 others(4): Show |
7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10591G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548884 | |||||||
chr1:206548904 | T | C | 28 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 others(25): Show |
29 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.579+10611T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548904 | |||||||
chr1:206548908 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+10615C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548908 | |||||||
chr1:206548928 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0005g0042 a0001c0001t0005g0164 others(4): Show |
10 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+10635C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206548928 | |||||||
chr1:206548958 | TG | T | 7 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0009g0030 others(4): Show |
7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+10668delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206548958 | ||||||
chr1:206549020 | C | T | 4 | a0001c0001t0003g0058 a0001c0001t0003g0152 a0001c0001t0003g0153 others(1): Show |
4 | HG02735.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+10727C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549020 | |||||||
chr1:206549117 | T | C | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 others(18): Show |
22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.579+10824T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549117 | |||||||
chr1:206549122 | TC | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(196): Show |
210 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.579+10830delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549122 | |||||||
chr1:206549125 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(196): Show |
210 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.579+10832C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549125 | |||||||
chr1:206549164 | C | G | 2 | a0001c0001t0003g0196 a0001c0001t0003g0211 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.579+10871C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549164 | |||||||
chr1:206549200 | C | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0029g0012 |
3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+10907C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549200 | |||||||
chr1:206549209 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 |
3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+10916T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549209 | |||||||
chr1:206549210 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.579+10917G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549210 | |||||||
chr1:206549410 | T | C | 18 | a0001c0001t0002g0119 a0001c0001t0006g0018 a0001c0001t0006g0033 others(15): Show |
19 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+11117T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549410 | |||||||
chr1:206549462 | A | G | 1 | a0001c0001t0006g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.579+11169A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549462 | |||||||
chr1:206549797 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+11504A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549797 | |||||||
chr1:206549928 | G | T | 7 | a0001c0001t0001g0147 a0001c0001t0002g0322 a0001c0001t0005g0224 others(4): Show |
7 | HG00099.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+11635G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206549928 | |||||||
chr1:206550475 | G | A | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.579+12182G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550475 | |||||||
chr1:206550586 | A | C | 4 | a0001c0004t0003g0103 a0001c0004t0030g0046 a0002c0005t0003g0186 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+12293A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550586 | |||||||
chr1:206550833 | A | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 |
3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+12540A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550833 | |||||||
chr1:206550909 | C | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(225): Show |
240 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(237): Show |
intron_variant | MODIFIER | c.579+12616C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550909 | |||||||
chr1:206550918 | C | T | 2 | a0001c0002t0004g0313 a0001c0002t0015g0318 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.579+12625C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206550918 | |||||||
chr1:206551038 | A | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(297): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.579+12745A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551038 | |||||||
chr1:206551326 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0059 |
3 | HG01069.hp1 HG01071.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.579+13033C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551326 | |||||||
chr1:206551331 | C | G | 9 | a0001c0001t0005g0207 a0001c0001t0011g0216 a0001c0002t0003g0035 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+13038C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551331 | |||||||
chr1:206551409 | G | A | 103 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0076 others(100): Show |
109 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(106): Show |
intron_variant | MODIFIER | c.579+13116G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551409 | |||||||
chr1:206551495 | G | A | 10 | a0001c0001t0001g0031 a0001c0001t0005g0042 a0001c0001t0005g0164 others(7): Show |
13 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+13202G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551495 | |||||||
chr1:206551566 | C | T | 1 | a0001c0001t0010g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.579+13273C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551566 | |||||||
chr1:206551583 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.579+13290C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551583 | |||||||
chr1:206551834 | A | C | 1 | a0007c0011t0006g0310 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.579+13541A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551834 | |||||||
chr1:206551911 | G | A | 4 | a0001c0004t0003g0103 a0001c0004t0030g0046 a0002c0005t0003g0186 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+13618G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551911 | |||||||
chr1:206551944 | A | G | 12 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(9): Show |
13 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+13651A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206551944 | |||||||
chr1:206552164 | G | A | 3 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0029g0012 |
3 | HG02922.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579+13871G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552164 | |||||||
chr1:206552560 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(200): Show |
214 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.579+14267C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552560 | |||||||
chr1:206552606 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+14313G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552606 | |||||||
chr1:206552816 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0245 a0001c0001t0009g0030 others(4): Show |
7 | HG02886.hp1 HG02896.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+14523G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206552816 | |||||||
chr1:206553119 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+14826G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553119 | |||||||
chr1:206553255 | G | A | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.579+14962G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553255 | |||||||
chr1:206553401 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.579+15108G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553401 | |||||||
chr1:206553440 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.579+15147A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553440 | |||||||
chr1:206553541 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.579+15248T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553541 | |||||||
chr1:206553660 | T | A | 136 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0063 others(133): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.579+15367T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553660 | |||||||
chr1:206553665 | G | C | 1 | a0001c0001t0012g0009 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579+15372G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553665 | |||||||
chr1:206553736 | C | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+15443C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553736 | |||||||
chr1:206553812 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(227): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.579+15519A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553812 | |||||||
chr1:206553932 | A | G | 63 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(60): Show |
65 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.579+15639A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206553932 | |||||||
chr1:206554054 | A | G | 7 | a0001c0001t0007g0032 a0001c0001t0007g0248 a0001c0001t0007g0249 others(4): Show |
11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+15761A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554054 | |||||||
chr1:206554076 | C | T | 65 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(62): Show |
67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+15783C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554076 | |||||||
chr1:206554107 | C | T | 65 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(62): Show |
67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+15814C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554107 | |||||||
chr1:206554117 | C | T | 142 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0063 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.579+15824C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554117 | |||||||
chr1:206554159 | TACA | T | 3 | a0001c0001t0001g0290 a0001c0002t0001g0283 a0001c0002t0001g0304 |
3 | HG01952.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.579+15867_579+1586 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554159 | |||||||
chr1:206554189 | A | T | 6 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(3): Show |
6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+15896A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554189 | |||||||
chr1:206554306 | T | A | 1 | a0001c0001t0002g0281 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.579+16013T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554306 | |||||||
chr1:206554307 | G | T | 1 | a0001c0001t0002g0281 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.579+16014G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554307 | |||||||
chr1:206554472 | C | T | 1 | a0001c0002t0009g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.579+16179C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554472 | |||||||
chr1:206554506 | G | A | 1 | a0001c0010t0003g0265 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.579+16213G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554506 | |||||||
chr1:206554646 | C | T | 65 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(62): Show |
67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+16353C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554646 | |||||||
chr1:206554706 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(150): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.579+16413C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206554706 | |||||||
chr1:206555055 | T | C | 2 | a0001c0001t0003g0010 a0001c0001t0004g0176 |
3 | NA18939.hp2 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.579+16762T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555055 | |||||||
chr1:206555366 | TG | T | 65 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(62): Show |
67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+17074delG | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555366 | |||||||
chr1:206555428 | G | A | 1 | a0001c0001t0011g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.579+17135G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555428 | |||||||
chr1:206555508 | G | GA | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+17218dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206555508 | ||||||
chr1:206555511 | A | AT | 65 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(62): Show |
67 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+17218_579+1721 others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555511 | |||||||
chr1:206555643 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.579+17350G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555643 | |||||||
chr1:206555654 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
74 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.579+17361C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555654 | |||||||
chr1:206555713 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+17420G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555713 | |||||||
chr1:206555776 | G | C | 2 | a0001c0004t0003g0103 a0001c0004t0030g0046 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.579+17483G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555776 | |||||||
chr1:206555776 | G | T | 1 | a0001c0002t0002g0144 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.579+17483G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555776 | |||||||
chr1:206555997 | G | A | 1 | a0001c0002t0009g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.579+17704G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206555997 | |||||||
chr1:206556234 | C | G | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+17941C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556234 | |||||||
chr1:206556265 | G | A | 83 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0147 others(80): Show |
86 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(83): Show |
intron_variant | MODIFIER | c.579+17972G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556265 | |||||||
chr1:206556294 | C | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(299): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.579+18001C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556294 | |||||||
chr1:206556334 | G | A | 1 | a0001c0001t0010g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.579+18041G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556334 | |||||||
chr1:206556372 | C | T | 3 | a0001c0001t0007g0248 a0001c0001t0007g0249 a0001c0001t0012g0009 |
4 | HG02572.hp2 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+18079C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556372 | |||||||
chr1:206556652 | G | A | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+18359G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556652 | |||||||
chr1:206556800 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.579+18507C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556800 | |||||||
chr1:206556810 | C | T | 1 | a0001c0001t0007g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.579+18517C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556810 | |||||||
chr1:206556818 | G | C | 2 | a0001c0001t0011g0117 a0001c0001t0011g0118 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+18525G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556818 | |||||||
chr1:206556980 | CA | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
71 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.579+18688delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206556980 | |||||||
chr1:206557278 | G | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0315 |
2 | HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.579+18985G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557278 | |||||||
chr1:206557313 | C | A | 76 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0147 others(73): Show |
79 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.579+19020C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557313 | |||||||
chr1:206557363 | G | C | 78 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0147 others(75): Show |
81 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.579+19070G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557363 | |||||||
chr1:206557420 | C | T | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+19127C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557420 | |||||||
chr1:206557732 | G | A | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+19439G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557732 | |||||||
chr1:206557763 | A | C | 1 | a0001c0004t0003g0103 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.579+19470A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206557763 | |||||||
chr1:206558116 | A | G | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+19823A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558116 | |||||||
chr1:206558119 | G | T | 1 | a0001c0002t0003g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.579+19826G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558119 | |||||||
chr1:206558288 | C | T | 20 | a0001c0001t0001g0027 a0001c0001t0002g0019 a0001c0001t0002g0020 others(17): Show |
21 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.579+19995C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558288 | |||||||
chr1:206558294 | T | C | 8 | a0001c0001t0001g0091 a0001c0001t0001g0149 a0001c0001t0001g0255 others(5): Show |
8 | HG01261.hp1 NA18747.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+20001T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558294 | |||||||
chr1:206558332 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.579+20039G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558332 | |||||||
chr1:206558539 | C | T | 1 | a0001c0002t0026g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.579+20246C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558539 | |||||||
chr1:206558669 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+20376C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558669 | |||||||
chr1:206558700 | A | G | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+20407A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558700 | |||||||
chr1:206558762 | G | A | 1 | a0006c0014t0001g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.579+20469G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206558762 | |||||||
chr1:206559098 | C | T | 27 | a0001c0001t0001g0027 a0001c0001t0002g0019 a0001c0001t0002g0020 others(24): Show |
28 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.579+20805C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559098 | |||||||
chr1:206559319 | G | A | 131 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.579+21026G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559319 | |||||||
chr1:206559507 | C | G | 9 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.579+21214C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559507 | |||||||
chr1:206559516 | C | A | 2 | a0001c0001t0002g0305 a0001c0007t0002g0221 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.579+21223C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559516 | |||||||
chr1:206559603 | T | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(165): Show |
182 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.579+21310T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559603 | |||||||
chr1:206559611 | C | T | 6 | a0001c0001t0003g0088 a0001c0001t0003g0139 a0001c0001t0003g0191 others(3): Show |
6 | HG00642.hp2 HG01358.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+21318C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559611 | |||||||
chr1:206559950 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+21657C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206559950 | |||||||
chr1:206560089 | C | T | 131 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.579+21796C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560089 | |||||||
chr1:206560368 | G | A | 6 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0004t0003g0103 others(3): Show |
6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+22075G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560368 | |||||||
chr1:206560382 | G | A | 2 | a0001c0008t0005g0107 a0001c0008t0005g0108 |
2 | HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.579+22089G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560382 | |||||||
chr1:206560386 | T | A | 1 | a0001c0001t0005g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.579+22093T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560386 | |||||||
chr1:206560443 | G | A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+22150G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560443 | |||||||
chr1:206560527 | G | A | 2 | a0001c0001t0016g0300 a0001c0001t0016g0301 |
2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.579+22234G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560527 | |||||||
chr1:206560716 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(62): Show |
71 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.579+22423T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206560716 | |||||||
chr1:206561064 | T | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-22205T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561064 | |||||||
chr1:206561175 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-22094C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561175 | |||||||
chr1:206561310 | C | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-21959C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561310 | |||||||
chr1:206561502 | T | C | 57 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0178 others(54): Show |
59 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.580-21767T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561502 | |||||||
chr1:206561579 | G | A | 57 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0178 others(54): Show |
59 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.580-21690G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561579 | |||||||
chr1:206561663 | C | CT | 13 | a0001c0001t0002g0225 a0001c0001t0005g0042 a0001c0001t0005g0164 others(10): Show |
13 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-21587dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | ||||||
chr1:206561663 | CT | C | 140 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0063 others(137): Show |
144 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.580-21587delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | ||||||
chr1:206561663 | CTT | C | 12 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0129 others(9): Show |
12 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-21588_580-2158 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561663 | ||||||
chr1:206561729 | G | A | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-21540G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561729 | |||||||
chr1:206561820 | C | A | 1 | a0001c0001t0002g0126 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.580-21449C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561820 | |||||||
chr1:206561840 | G | GTT | 136 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(133): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.580-21419_580-2141 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561840 | ||||||
chr1:206561840 | G | GTTT | 10 | a0001c0001t0001g0027 a0001c0001t0002g0129 a0001c0001t0002g0130 others(7): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.580-21420_580-2141 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206561840 | ||||||
chr1:206561869 | C | T | 6 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0004t0003g0103 others(3): Show |
6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-21400C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561869 | |||||||
chr1:206561915 | A | G | 17 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(14): Show |
17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-21354A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206561915 | |||||||
chr1:206562363 | C | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(166): Show |
179 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.580-20906C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562363 | |||||||
chr1:206562529 | C | G | 309 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(306): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.580-20740C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562529 | |||||||
chr1:206562532 | G | A | 6 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0004t0003g0103 others(3): Show |
6 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-20737G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562532 | |||||||
chr1:206562660 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(167): Show |
180 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.580-20609T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562660 | |||||||
chr1:206562708 | G | T | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-20561G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562708 | |||||||
chr1:206562714 | C | T | 1 | a0001c0004t0030g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.580-20555C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562714 | |||||||
chr1:206562760 | A | G | 17 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(14): Show |
17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-20509A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562760 | |||||||
chr1:206562814 | T | C | 310 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(307): Show |
327 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.580-20455T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562814 | |||||||
chr1:206562843 | A | T | 2 | a0001c0002t0015g0243 a0001c0002t0015g0318 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.580-20426A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562843 | |||||||
chr1:206562871 | A | G | 17 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(14): Show |
17 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-20398A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562871 | |||||||
chr1:206562880 | C | T | 1 | a0001c0001t0005g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.580-20389C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562880 | |||||||
chr1:206562885 | G | A | 9 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-20384G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562885 | |||||||
chr1:206562912 | T | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(143): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.580-20357T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206562912 | |||||||
chr1:206562921 | CA | C | 62 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(59): Show |
64 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(61): Show |
intron_variant | MODIFIER | c.580-20337delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206562921 | ||||||
chr1:206563245 | G | A | 131 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(128): Show |
134 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.580-20024G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563245 | |||||||
chr1:206563267 | G | C | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-20002G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563267 | |||||||
chr1:206563332 | A | G | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(4): Show |
7 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-19937A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563332 | |||||||
chr1:206563346 | C | A | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-19923C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563346 | |||||||
chr1:206563368 | T | C | 1 | a0001c0016t0002g0132 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.580-19901T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563368 | |||||||
chr1:206563601 | C | A | 2 | a0001c0002t0003g0241 a0001c0002t0026g0043 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.580-19668C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563601 | |||||||
chr1:206563914 | C | A | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(16): Show |
19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-19355C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563914 | |||||||
chr1:206563929 | T | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(147): Show |
160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.580-19340T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563929 | |||||||
chr1:206563948 | A | C | 30 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(27): Show |
31 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-19321A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206563948 | |||||||
chr1:206564308 | G | T | 4 | a0001c0002t0003g0241 a0001c0002t0009g0008 a0001c0002t0009g0160 others(1): Show |
5 | HG02145.hp2 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-18961G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564308 | |||||||
chr1:206564369 | C | A | 1 | a0001c0001t0008g0158 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.580-18900C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564369 | |||||||
chr1:206564540 | C | T | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-18729C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564540 | |||||||
chr1:206564823 | G | C | 10 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0048 others(7): Show |
10 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-18446G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564823 | |||||||
chr1:206564952 | C | G | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-18317C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206564952 | |||||||
chr1:206565031 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01346.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.580-18238G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565031 | |||||||
chr1:206565135 | C | T | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-18134C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565135 | |||||||
chr1:206565257 | C | T | 11 | a0001c0001t0001g0027 a0001c0001t0002g0129 a0001c0001t0002g0130 others(8): Show |
12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-18012C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565257 | |||||||
chr1:206565258 | A | G | 310 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(307): Show |
327 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.580-18011A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565258 | |||||||
chr1:206565542 | G | C | 1 | a0001c0001t0003g0254 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-17727G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565542 | |||||||
chr1:206565545 | T | C | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(16): Show |
19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-17724T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565545 | |||||||
chr1:206565672 | A | T | 19 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(16): Show |
19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.580-17597A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565672 | |||||||
chr1:206565675 | G | C | 9 | a0001c0001t0005g0207 a0001c0001t0007g0032 a0001c0001t0007g0248 others(6): Show |
13 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-17594G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565675 | |||||||
chr1:206565781 | C | T | 1 | a0001c0001t0002g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580-17488C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565781 | |||||||
chr1:206565959 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0006g0306 a0001c0001t0006g0316 others(1): Show |
4 | HG01257.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-17310C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206565959 | |||||||
chr1:206566018 | A | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(306): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.580-17251A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566018 | |||||||
chr1:206566084 | C | T | 4 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0008t0005g0107 others(1): Show |
4 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-17185C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566084 | |||||||
chr1:206566196 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0003g0270 |
2 | NA18951.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.580-17073G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566196 | |||||||
chr1:206566230 | C | T | 9 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0002t0003g0035 others(6): Show |
9 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-17039C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566230 | |||||||
chr1:206566235 | A | G | 1 | a0001c0002t0009g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-17034A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566235 | |||||||
chr1:206566276 | T | G | 1 | a0001c0001t0018g0285 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-16993T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566276 | |||||||
chr1:206566431 | C | T | 15 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0207 others(12): Show |
19 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-16838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566431 | |||||||
chr1:206566437 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(159): Show |
172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.580-16832T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566437 | |||||||
chr1:206566541 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.580-16728G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566541 | |||||||
chr1:206566677 | A | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(174): Show |
191 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.580-16592A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566677 | |||||||
chr1:206566691 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0280 |
2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.580-16578C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566691 | |||||||
chr1:206566692 | G | A | 8 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0001t0009g0030 others(5): Show |
8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-16577G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566692 | |||||||
chr1:206566731 | A | C | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-16538A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566731 | |||||||
chr1:206566763 | A | T | 1 | a0001c0002t0009g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580-16506A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566763 | |||||||
chr1:206566794 | C | T | 1 | a0001c0001t0010g0146 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.580-16475C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206566794 | |||||||
chr1:206567232 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(142): Show |
155 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.580-16037C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567232 | |||||||
chr1:206567420 | T | C | 6 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(3): Show |
6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-15849T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567420 | |||||||
chr1:206567472 | A | G | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-15797A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567472 | |||||||
chr1:206567473 | T | C | 2 | a0001c0002t0004g0259 a0001c0002t0004g0282 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.580-15796T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567473 | |||||||
chr1:206567712 | A | G | 2 | a0004c0009t0001g0045 a0004c0009t0001g0291 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.580-15557A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567712 | |||||||
chr1:206567714 | G | A | 8 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0001t0009g0030 others(5): Show |
8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-15555G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567714 | |||||||
chr1:206567915 | C | T | 1 | a0001c0002t0006g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580-15354C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206567915 | |||||||
chr1:206568018 | G | A | 4 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(1): Show |
4 | HG01109.hp2 HG02109.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-15251G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568018 | |||||||
chr1:206568218 | G | C | 1 | a0001c0001t0007g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.580-15051G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568218 | |||||||
chr1:206568246 | A | G | 1 | a0001c0001t0003g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.580-15023A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568246 | |||||||
chr1:206568266 | T | C | 8 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0001t0009g0030 others(5): Show |
8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-15003T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568266 | |||||||
chr1:206568324 | C | T | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-14945C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568324 | |||||||
chr1:206568536 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.580-14733C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568536 | |||||||
chr1:206568589 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(174): Show |
191 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.580-14680A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568589 | |||||||
chr1:206568633 | G | A | 1 | a0001c0001t0018g0285 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-14636G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568633 | |||||||
chr1:206568681 | A | G | 8 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0001t0009g0030 others(5): Show |
8 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-14588A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568681 | |||||||
chr1:206568780 | G | T | 1 | a0001c0002t0002g0144 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.580-14489G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568780 | |||||||
chr1:206568852 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(166): Show |
183 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.580-14417A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568852 | |||||||
chr1:206568856 | T | C | 1 | a0001c0001t0002g0281 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.580-14413T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568856 | |||||||
chr1:206568889 | G | A | 2 | a0001c0002t0009g0008 a0001c0002t0009g0160 |
3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-14380G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568889 | |||||||
chr1:206568935 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(62): Show |
71 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.580-14334C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206568935 | |||||||
chr1:206569074 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(151): Show |
164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.580-14195C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569074 | |||||||
chr1:206569146 | T | C | 1 | a0001c0002t0009g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-14123T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569146 | |||||||
chr1:206569371 | A | C | 4 | a0001c0004t0003g0103 a0001c0004t0030g0046 a0002c0005t0003g0186 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-13898A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569371 | |||||||
chr1:206569431 | C | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(170): Show |
187 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.580-13838C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569431 | |||||||
chr1:206569612 | G | A | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.580-13657G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569612 | |||||||
chr1:206569739 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.580-13530T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569739 | |||||||
chr1:206569902 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13367G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569902 | |||||||
chr1:206569906 | T | A | 5 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0004t0024g0023 others(2): Show |
5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-13363T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206569906 | |||||||
chr1:206570061 | C | G | 5 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0004t0024g0023 others(2): Show |
5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-13208C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570061 | |||||||
chr1:206570078 | CT | C | 25 | a0001c0001t0001g0031 a0001c0001t0001g0127 a0001c0001t0001g0149 others(22): Show |
25 | HG00597.hp2 HG01109.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-13165delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570078 | CTT | C | 96 | a0001c0001t0001g0063 a0001c0001t0001g0080 a0001c0001t0001g0091 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.580-13166_580-1316 others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570078 | CTTT | C | 14 | a0001c0001t0001g0101 a0001c0001t0002g0246 a0001c0001t0003g0058 others(11): Show |
14 | HG02698.hp2 HG02735.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-13167_580-1316 others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570078 | CTTTTTTT others(1): Show |
C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
85 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.580-13172_580-1316 others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570078 | CTTTTTTT others(2): Show |
C | 89 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0147 others(86): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.580-13173_580-1316 others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570078 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-13174_580-1316 others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206570078 | ||||||
chr1:206570104 | T | C | 3 | a0001c0001t0003g0213 a0001c0001t0003g0214 a0001c0001t0003g0215 |
3 | NA18979.hp1 NA18985.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.580-13165T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570104 | |||||||
chr1:206570112 | A | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13157A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570112 | |||||||
chr1:206570241 | A | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-13028A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570241 | |||||||
chr1:206570248 | C | G | 1 | a0001c0003t0005g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.580-13021C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570248 | |||||||
chr1:206570337 | T | G | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-12932T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570337 | |||||||
chr1:206570464 | C | T | 5 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0004t0024g0023 others(2): Show |
5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-12805C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570464 | |||||||
chr1:206570498 | A | G | 1 | a0001c0003t0005g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580-12771A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570498 | |||||||
chr1:206570710 | C | T | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-12559C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570710 | |||||||
chr1:206570732 | T | C | 1 | a0001c0002t0004g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.580-12537T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570732 | |||||||
chr1:206570863 | C | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(165): Show |
182 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.580-12406C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570863 | |||||||
chr1:206570890 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.580-12379G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570890 | |||||||
chr1:206570960 | T | C | 1 | a0001c0001t0011g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-12309T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206570960 | |||||||
chr1:206571007 | A | G | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-12262A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571007 | |||||||
chr1:206571094 | G | C | 2 | a0001c0001t0003g0286 a0001c0001t0018g0285 |
2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.580-12175G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571094 | |||||||
chr1:206571260 | T | A | 1 | a0001c0001t0002g0130 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.580-12009T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571260 | |||||||
chr1:206571283 | G | GT | 162 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(159): Show |
172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.580-11975dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206571283 | ||||||
chr1:206571283 | GT | G | 6 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0006g0036 others(3): Show |
6 | HG01109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-11975delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206571283 | ||||||
chr1:206571302 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11967G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571302 | |||||||
chr1:206571305 | A | T | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11964A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571305 | |||||||
chr1:206571306 | G | C | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11963G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571306 | |||||||
chr1:206571412 | G | A | 5 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-11857G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571412 | |||||||
chr1:206571446 | C | T | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-11823C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571446 | |||||||
chr1:206571585 | G | A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-11684G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206571585 | |||||||
chr1:206572038 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.580-11231T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572038 | |||||||
chr1:206572185 | C | A | 46 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(43): Show |
48 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.580-11084C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572185 | |||||||
chr1:206572195 | CTTCT | C | 54 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(51): Show |
56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-11071_580-1106 others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206572195 | ||||||
chr1:206572273 | G | A | 7 | a0001c0001t0007g0032 a0001c0001t0007g0248 a0001c0001t0007g0249 others(4): Show |
11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-10996G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572273 | |||||||
chr1:206572297 | C | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-10972C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572297 | |||||||
chr1:206572397 | T | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(164): Show |
181 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.580-10872T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572397 | |||||||
chr1:206572468 | G | T | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10801G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572468 | |||||||
chr1:206572469 | T | A | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10800T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572469 | |||||||
chr1:206572510 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-10759C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572510 | |||||||
chr1:206572606 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0314 a0001c0001t0005g0042 others(4): Show |
7 | HG01952.hp2 HG01978.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-10663C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572606 | |||||||
chr1:206572650 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10619C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572650 | |||||||
chr1:206572667 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10602C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572667 | |||||||
chr1:206572673 | T | C | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-10596T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572673 | |||||||
chr1:206572797 | A | G | 30 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(27): Show |
31 | HG00558.hp2 HG00642.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-10472A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572797 | |||||||
chr1:206572855 | A | G | 1 | a0001c0001t0002g0297 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.580-10414A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572855 | |||||||
chr1:206572908 | C | T | 1 | a0001c0001t0017g0047 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.580-10361C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572908 | |||||||
chr1:206572909 | G | A | 8 | a0001c0002t0004g0168 a0001c0002t0004g0169 a0001c0002t0004g0170 others(5): Show |
8 | HG02129.hp2 HG02165.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-10360G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206572909 | |||||||
chr1:206573024 | C | G | 1 | a0001c0001t0005g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.580-10245C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573024 | |||||||
chr1:206573042 | G | A | 1 | a0001c0001t0003g0095 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.580-10227G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573042 | |||||||
chr1:206573062 | C | T | 5 | a0001c0001t0013g0002 a0001c0001t0013g0052 a0001c0001t0013g0053 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-10207C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573062 | |||||||
chr1:206573063 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.580-10206G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573063 | |||||||
chr1:206573094 | T | C | 1 | a0001c0002t0006g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.580-10175T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573094 | |||||||
chr1:206573116 | G | C | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-10153G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573116 | |||||||
chr1:206573261 | A | C | 1 | a0001c0001t0002g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.580-10008A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573261 | |||||||
chr1:206573537 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(143): Show |
156 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.580-9732A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573537 | |||||||
chr1:206573713 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(164): Show |
181 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.580-9556A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573713 | |||||||
chr1:206573721 | T | C | 1 | a0001c0001t0011g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-9548T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573721 | |||||||
chr1:206573923 | C | G | 5 | a0001c0001t0001g0039 a0001c0001t0012g0161 a0002c0005t0001g0183 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-9346C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206573923 | |||||||
chr1:206574048 | A | G | 131 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(128): Show |
134 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.580-9221A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574048 | |||||||
chr1:206574130 | A | G | 298 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(295): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.580-9139A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574130 | |||||||
chr1:206574375 | C | T | 1 | a0001c0001t0004g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.580-8894C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574375 | |||||||
chr1:206574456 | C | G | 2 | a0001c0002t0015g0243 a0001c0002t0015g0318 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.580-8813C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574456 | |||||||
chr1:206574617 | G | A | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-8652G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206574617 | |||||||
chr1:206574853 | C | CT | 58 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0079 others(55): Show |
60 | HG00423.hp1 HG01175.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.580-8392dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | ||||||
chr1:206574853 | CT | C | 134 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(131): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.580-8392delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | ||||||
chr1:206574853 | CTT | C | 7 | a0001c0001t0003g0094 a0001c0001t0003g0153 a0001c0001t0005g0207 others(4): Show |
7 | HG01975.hp1 HG01993.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8393_580-8392d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206574853 | ||||||
chr1:206575008 | C | T | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-8261C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575008 | |||||||
chr1:206575009 | G | A | 2 | a0001c0001t0006g0018 a0001c0001t0006g0311 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.580-8260G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575009 | |||||||
chr1:206575027 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-8242T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575027 | |||||||
chr1:206575039 | T | TG | 147 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(144): Show |
157 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.580-8230_580-8229i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575039 | |||||||
chr1:206575039 | T | TGTTTTTG | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-8230_580-8229i others(9): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575039 | |||||||
chr1:206575097 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(148): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.580-8172C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575097 | |||||||
chr1:206575167 | C | T | 1 | a0002c0013t0004g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.580-8102C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575167 | |||||||
chr1:206575339 | CAG | C | 7 | a0001c0001t0007g0032 a0001c0001t0007g0248 a0001c0001t0007g0249 others(4): Show |
11 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-7928_580-7927d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206575339 | ||||||
chr1:206575453 | G | C | 2 | a0001c0001t0005g0224 a0001c0008t0005g0107 |
2 | HG00099.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.580-7816G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575453 | |||||||
chr1:206575513 | A | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(149): Show |
162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.580-7756A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575513 | |||||||
chr1:206575583 | C | T | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-7686C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575583 | |||||||
chr1:206575707 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.580-7562G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575707 | |||||||
chr1:206575790 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-7479G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575790 | |||||||
chr1:206575854 | C | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(166): Show |
183 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.580-7415C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206575854 | |||||||
chr1:206576009 | A | T | 7 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.580-7260A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576009 | |||||||
chr1:206576196 | C | T | 6 | a0001c0001t0002g0322 a0001c0001t0010g0077 a0001c0001t0010g0146 others(3): Show |
6 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-7073C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576196 | |||||||
chr1:206576202 | C | T | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-7067C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576202 | |||||||
chr1:206576309 | A | C | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-6960A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576309 | |||||||
chr1:206576360 | G | A | 298 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(295): Show |
316 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.580-6909G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576360 | |||||||
chr1:206576839 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-6430T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576839 | |||||||
chr1:206576970 | A | G | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-6299A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576970 | |||||||
chr1:206576974 | T | C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-6295T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206576974 | |||||||
chr1:206576978 | A | AT | 193 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(190): Show |
206 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.580-6278dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206576978 | ||||||
chr1:206576978 | AT | A | 6 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-6278delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206576978 | ||||||
chr1:206577389 | C | G | 15 | a0001c0002t0001g0069 a0001c0002t0001g0121 a0001c0002t0002g0144 others(12): Show |
15 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.580-5880C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577389 | |||||||
chr1:206577443 | AT | A | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0003g0241 others(4): Show |
7 | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-5823delT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206577443 | ||||||
chr1:206577458 | T | A | 1 | a0001c0004t0007g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.580-5811T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577458 | |||||||
chr1:206577564 | T | C | 1 | a0001c0007t0002g0222 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580-5705T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577564 | |||||||
chr1:206577672 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.580-5597C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577672 | |||||||
chr1:206577673 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5596G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577673 | |||||||
chr1:206577776 | A | G | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-5493A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577776 | |||||||
chr1:206577831 | G | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.580-5438G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577831 | |||||||
chr1:206577980 | C | T | 284 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(281): Show |
298 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(295): Show |
intron_variant | MODIFIER | c.580-5289C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206577980 | |||||||
chr1:206578069 | T | TA | 141 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.580-5192dupA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578069 | ||||||
chr1:206578073 | A | AT | 6 | a0001c0001t0002g0322 a0001c0001t0010g0077 a0001c0001t0010g0146 others(3): Show |
6 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.580-5196_580-5195i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578073 | |||||||
chr1:206578103 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(144): Show |
158 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.580-5166G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578103 | |||||||
chr1:206578115 | AC | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
73 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.580-5153delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578115 | |||||||
chr1:206578174 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.580-5095T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578174 | |||||||
chr1:206578202 | G | C | 9 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-5067G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578202 | |||||||
chr1:206578222 | CA | C | 18 | a0001c0001t0001g0055 a0001c0001t0001g0122 a0001c0001t0001g0197 others(15): Show |
19 | HG01515.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-5036delA | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578222 | ||||||
chr1:206578232 | A | AG | 36 | a0001c0001t0001g0266 a0001c0001t0002g0015 a0001c0001t0002g0016 others(33): Show |
38 | HG00423.hp1 HG01175.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.580-5037_580-5036i others(3): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | |||||||
chr1:206578232 | A | AGTG | 14 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0296 others(11): Show |
14 | HG00438.hp1 HG02647.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-5037_580-5036i others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | |||||||
chr1:206578232 | A | AGTGTG | 3 | a0001c0001t0006g0033 a0001c0001t0006g0034 a0002c0005t0028g0208 |
3 | HG02055.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.580-5037_580-5036i others(7): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | |||||||
chr1:206578232 | A | AGTGTGTG others(4): Show |
1 | a0001c0001t0006g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.580-5037_580-5036i others(13): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | |||||||
chr1:206578232 | AAGT | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(65): Show |
75 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.580-5036_580-5034d others(5): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578232 | |||||||
chr1:206578233 | A | AGAGT | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5035_580-5034i others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | AGT | 18 | a0001c0001t0001g0195 a0001c0001t0001g0206 a0001c0001t0003g0044 others(15): Show |
22 | HG00741.hp2 HG01884.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.580-5007_580-5006d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | AGTGT | 20 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0003g0058 others(17): Show |
21 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.580-5009_580-5006d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | AGTGTGT | 16 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0314 others(13): Show |
16 | HG00642.hp2 HG01358.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-5011_580-5006d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | AGTGTGTG others(1): Show |
35 | a0001c0001t0001g0112 a0001c0001t0002g0203 a0001c0001t0003g0005 others(32): Show |
35 | HG00597.hp2 HG00609.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.580-5013_580-5006d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0003g0125 a0001c0001t0003g0140 a0001c0001t0003g0286 |
3 | HG00621.hp1 HG02698.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.580-5015_580-5006d others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578233 | A | T | 57 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(54): Show |
60 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.580-5036A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578233 | |||||||
chr1:206578233 | AGTGT | A | 4 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0008t0005g0107 others(1): Show |
4 | HG00099.hp1 HG01978.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-5009_580-5006d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578233 | ||||||
chr1:206578260 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0003g0245 a0001c0001t0003g0324 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.580-5006_580-5005i others(12): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206578260 | ||||||
chr1:206578295 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.580-4974T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578295 | |||||||
chr1:206578477 | C | T | 16 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(13): Show |
20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-4792C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578477 | |||||||
chr1:206578559 | G | A | 1 | a0001c0003t0002g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.580-4710G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578559 | |||||||
chr1:206578794 | G | A | 1 | a0001c0001t0002g0016 | 2 | HG02300.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.580-4475G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578794 | |||||||
chr1:206578952 | T | A | 1 | a0001c0001t0012g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.580-4317T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206578952 | |||||||
chr1:206579256 | T | C | 1 | a0001c0002t0004g0313 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.580-4013T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579256 | |||||||
chr1:206579301 | A | G | 2 | a0001c0002t0009g0008 a0001c0002t0009g0160 |
3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-3968A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579301 | |||||||
chr1:206579333 | C | T | 7 | a0001c0002t0003g0035 a0001c0002t0003g0037 a0001c0002t0003g0241 others(4): Show |
7 | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-3936C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579333 | |||||||
chr1:206579339 | C | G | 1 | a0001c0001t0002g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.580-3930C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579339 | |||||||
chr1:206579396 | G | T | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3873G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579396 | |||||||
chr1:206579400 | C | T | 2 | a0001c0002t0009g0008 a0001c0002t0009g0160 |
3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.580-3869C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579400 | |||||||
chr1:206579514 | G | A | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-3755G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579514 | |||||||
chr1:206579515 | T | G | 1 | a0001c0001t0003g0309 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-3754T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579515 | |||||||
chr1:206579571 | A | T | 1 | a0002c0013t0004g0209 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.580-3698A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579571 | |||||||
chr1:206579636 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.580-3633G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579636 | |||||||
chr1:206579661 | A | AT | 16 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(13): Show |
20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-3603dupT | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206579661 | ||||||
chr1:206579679 | C | T | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-3590C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579679 | |||||||
chr1:206579697 | C | A | 1 | a0001c0001t0002g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.580-3572C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579697 | |||||||
chr1:206579763 | T | C | 1 | a0001c0001t0011g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.580-3506T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579763 | |||||||
chr1:206579804 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-3465A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579804 | |||||||
chr1:206579816 | T | C | 8 | a0001c0001t0007g0032 a0001c0001t0007g0248 a0001c0001t0007g0249 others(5): Show |
12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-3453T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579816 | |||||||
chr1:206579832 | T | A | 8 | a0001c0001t0007g0032 a0001c0001t0007g0248 a0001c0001t0007g0249 others(5): Show |
12 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-3437T>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206579832 | |||||||
chr1:206579844 | C | CGTGGCT | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3417_580-3412d others(8): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206579844 | ||||||
chr1:206580145 | G | T | 3 | a0001c0002t0009g0008 a0001c0002t0009g0160 a0001c0002t0026g0043 |
4 | HG02622.hp1 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3124G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580145 | |||||||
chr1:206580154 | G | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.580-3115G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580154 | |||||||
chr1:206580418 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.580-2851C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580418 | |||||||
chr1:206580443 | T | C | 54 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(51): Show |
56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-2826T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580443 | |||||||
chr1:206580465 | T | G | 47 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0149 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.580-2804T>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580465 | |||||||
chr1:206580631 | G | A | 14 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0001t0007g0032 others(11): Show |
18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.580-2638G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580631 | |||||||
chr1:206580705 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2564G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580705 | |||||||
chr1:206580736 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2533T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580736 | |||||||
chr1:206580849 | C | T | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-2420C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580849 | |||||||
chr1:206580874 | G | C | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.580-2395G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580874 | |||||||
chr1:206580883 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-2386C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580883 | |||||||
chr1:206580949 | C | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.580-2320C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206580949 | |||||||
chr1:206581014 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.580-2255C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581014 | |||||||
chr1:206581032 | G | A | 8 | a0001c0001t0003g0244 a0001c0001t0006g0018 a0001c0001t0006g0033 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-2237G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581032 | |||||||
chr1:206581266 | G | A | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-2003G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581266 | |||||||
chr1:206581295 | T | C | 299 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(296): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.580-1974T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581295 | |||||||
chr1:206581427 | G | A | 54 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(51): Show |
56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.580-1842G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581427 | |||||||
chr1:206581458 | G | A | 8 | a0001c0001t0003g0244 a0001c0001t0006g0018 a0001c0001t0006g0033 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1811G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581458 | |||||||
chr1:206581561 | T | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(285): Show |
306 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(303): Show |
intron_variant | MODIFIER | c.580-1708T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581561 | |||||||
chr1:206581562 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580-1707G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581562 | |||||||
chr1:206581596 | A | AAAAG | 16 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0005g0042 others(13): Show |
20 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.580-1659_580-1656d others(6): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581596 | ||||||
chr1:206581622 | CAG | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(63): Show |
73 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.580-1638_580-1637d others(4): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581622 | ||||||
chr1:206581638 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-1631A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581638 | |||||||
chr1:206581672 | G | GAAAAGAA others(5): Show |
2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.580-1597_580-1596i others(14): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581672 | |||||||
chr1:206581672 | G | GGAAAGAA others(1): Show |
22 | a0001c0001t0003g0244 a0001c0001t0005g0042 a0001c0001t0005g0164 others(19): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-1591_580-1584d others(10): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr1 | 206581672 | ||||||
chr1:206581676 | A | G | 1 | a0001c0001t0002g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.580-1593A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581676 | |||||||
chr1:206581734 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.580-1535G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581734 | |||||||
chr1:206581797 | G | A | 4 | a0001c0001t0009g0030 a0001c0001t0009g0051 a0001c0001t0009g0056 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1472G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581797 | |||||||
chr1:206581824 | G | T | 8 | a0001c0001t0003g0244 a0001c0001t0006g0018 a0001c0001t0006g0033 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-1445G>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581824 | |||||||
chr1:206581883 | G | C | 5 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0008t0005g0107 others(2): Show |
5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-1386G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581883 | |||||||
chr1:206581914 | A | G | 297 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(294): Show |
315 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.580-1355A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581914 | |||||||
chr1:206581920 | C | T | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-1349C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581920 | |||||||
chr1:206581921 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.580-1348G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581921 | |||||||
chr1:206581922 | TC | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0296 others(7): Show |
10 | HG01358.hp2 HG02083.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-1346delC | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581922 | |||||||
chr1:206581945 | A | G | 1 | a0001c0001t0021g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.580-1324A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206581945 | |||||||
chr1:206582031 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.580-1238G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582031 | |||||||
chr1:206582056 | T | C | 2 | a0001c0001t0005g0042 a0001c0001t0005g0164 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.580-1213T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582056 | |||||||
chr1:206582515 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.580-754T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582515 | |||||||
chr1:206582535 | G | A | 126 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0080 others(123): Show |
129 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.580-734G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582535 | |||||||
chr1:206582651 | G | A | 22 | a0001c0001t0003g0244 a0001c0001t0005g0042 a0001c0001t0005g0164 others(19): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-618G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582651 | |||||||
chr1:206582679 | T | C | 11 | a0001c0001t0001g0027 a0001c0001t0002g0129 a0001c0001t0002g0130 others(8): Show |
12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-590T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582679 | |||||||
chr1:206582745 | C | G | 8 | a0001c0001t0003g0244 a0001c0001t0006g0018 a0001c0001t0006g0033 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-524C>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582745 | |||||||
chr1:206582870 | G | A | 16 | a0001c0001t0001g0266 a0001c0001t0002g0024 a0001c0001t0002g0097 others(13): Show |
16 | HG00438.hp1 NA18612.hp2 NA18948.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-399G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206582870 | |||||||
chr1:206583062 | A | G | 1 | a0006c0014t0001g0082 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.580-207A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583062 | |||||||
chr1:206583130 | C | T | 14 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0001t0007g0032 others(11): Show |
18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.580-139C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583130 | |||||||
chr1:206583181 | T | C | 1 | a0001c0001t0002g0276 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.580-88T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583181 | |||||||
chr1:206583202 | C | T | 5 | a0001c0001t0005g0048 a0001c0001t0005g0224 a0001c0008t0005g0107 others(2): Show |
5 | HG00099.hp1 HG01952.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-67C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 2/5 | chr1 | 206583202 | |||||||
chr1:206583401 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.690+22A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583401 | |||||||
chr1:206583497 | C | T | 2 | a0001c0001t0005g0207 a0001c0004t0005g0021 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.690+118C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583497 | |||||||
chr1:206583738 | C | T | 54 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0266 others(51): Show |
56 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.690+359C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583738 | |||||||
chr1:206583773 | G | A | 14 | a0001c0001t0005g0042 a0001c0001t0005g0164 a0001c0001t0007g0032 others(11): Show |
18 | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+394G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583773 | |||||||
chr1:206583792 | C | T | 1 | a0001c0004t0024g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.690+413C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206583792 | |||||||
chr1:206584071 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.691-316A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584071 | |||||||
chr1:206584099 | C | A | 7 | a0001c0001t0006g0018 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
8 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.691-288C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584099 | |||||||
chr1:206584116 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.691-271C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 3/5 | chr1 | 206584116 | |||||||
chr1:206584745 | A | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0050 others(80): Show |
85 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.988+61A>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584745 | |||||||
chr1:206584760 | G | A | 7 | a0001c0001t0002g0322 a0001c0001t0005g0218 a0001c0001t0010g0077 others(4): Show |
7 | HG01361.hp2 HG02132.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+76G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584760 | |||||||
chr1:206584824 | A | G | 1 | a0001c0002t0004g0175 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.988+140A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206584824 | |||||||
chr1:206584883 | CAGGAAAA others(9): Show |
C | 1 | a0001c0001t0014g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.988+203_988+218del others(16): Show |
RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr1 | 206584883 | ||||||
chr1:206585161 | A | C | 5 | a0001c0001t0009g0051 a0001c0001t0009g0056 a0001c0001t0009g0181 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.989-19A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 4/5 | chr1 | 206585161 | |||||||
chr1:206585641 | C | T | 10 | a0001c0001t0005g0210 a0001c0003t0005g0060 a0001c0003t0005g0180 others(7): Show |
10 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1104+346C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585641 | |||||||
chr1:206585774 | C | A | 149 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0024 others(146): Show |
156 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.1104+479C>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585774 | |||||||
chr1:206585843 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1104+548C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585843 | |||||||
chr1:206585994 | C | T | 1 | a0001c0002t0026g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1104+699C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206585994 | |||||||
chr1:206586266 | A | C | 197 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0019 others(194): Show |
209 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1105-560A>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586266 | |||||||
chr1:206586290 | A | G | 197 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0019 others(194): Show |
209 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1105-536A>G | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586290 | |||||||
chr1:206586305 | G | C | 73 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0010 others(70): Show |
77 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1105-521G>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586305 | |||||||
chr1:206586451 | G | A | 76 | a0001c0001t0001g0290 a0001c0001t0003g0005 a0001c0001t0003g0006 others(73): Show |
80 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1105-375G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586451 | |||||||
chr1:206586532 | T | C | 232 | a0001c0001t0001g0178 a0001c0001t0002g0015 a0001c0001t0002g0016 others(229): Show |
244 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1105-294T>C | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586532 | |||||||
chr1:206586643 | G | A | 74 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0024 others(71): Show |
77 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1105-183G>A | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586643 | |||||||
chr1:206586816 | C | T | 1 | a0001c0008t0005g0108 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1105-10C>T | RASSF5 | ENSG00000266094.8 | transcript | ENST00000579436.7 | protein_coding | 5/5 | chr1 | 206586816 |