Item | Value |
---|---|
geneid | 51773 |
ensemblid | ENSG00000048649.14 |
hgncid | 18118 |
symbol | RSF1 |
name | remodeling and spacing factor 1 |
refseq_nuc | NM_016578.4 |
refseq_prot | NP_057662.3 |
ensembl_nuc | ENST00000308488.11 |
ensembl_prot | ENSP00000311513.6 |
mane_status | MANE Select |
chr | chr11 |
start | 77660009 |
end | 77820722 |
strand | - |
ver | v1.2 |
region | chr11:77660009-77820722 |
region5000 | chr11:77655009-77825722 |
regionname0 | RSF1_chr11_77660009_77820722 |
regionname5000 | RSF1_chr11_77655009_77825722 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1441 | 292 | 75 | 43 | 143 | 11 | 18 | 108 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0002 | 0/0 | 1441 | 45 | 3 | 13 | 13 | 4 | 12 | 8 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0003 | 0/0 | 1441 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0004 | 0/0 | 1441 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0005 | 0/0 | 1441 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0006 | 0/0 | 1441 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0007 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0008 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0009 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0010 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0011 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
a0012 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | MATAA others(1436): Show |
chr11 | 77655009 | 77825722 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4323 | 211 | 50 | 30 | 101 | 10 | 18 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0001c0002 | 0/0 | 4323 | 78 | 24 | 12 | 41 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0001c0009 | 0/0 | 4323 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0001c0010 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0001c0017 | 0/0 | 4323 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0002c0003 | 0/0 | 4323 | 40 | 3 | 13 | 8 | 4 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0002c0004 | 0/0 | 4323 | 5 | 0 | 0 | 5 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0003c0005 | 0/0 | 4323 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0003c0016 | 0/0 | 4323 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0004c0006 | 0/0 | 4323 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0005c0007 | 0/0 | 4323 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0006c0015 | 0/0 | 4323 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0007c0012 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0008c0011 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0009c0014 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0010c0013 | 0/0 | 4323 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0011c0018 | 0/0 | 4323 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 | ||
a0012c0008 | 0/0 | 4323 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | ATGGC others(4318): Show |
chr11 | 77655009 | 77825722 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 11245 | 71 | 15 | 8 | 41 | 5 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0002 | 0/0 | 11243 | 21 | 13 | 0 | 7 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0004 | 1/0 | 11242 | 49 | 1 | 10 | 22 | 3 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0005 | 0/0 | 11245 | 9 | 0 | 1 | 8 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0006 | 0/0 | 11243 | 6 | 5 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0007 | 0/0 | 11240 | 4 | 0 | 0 | 4 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11235): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0008 | 0/0 | 11245 | 4 | 0 | 3 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0009 | 0/0 | 11243 | 4 | 4 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0011 | 0/0 | 11242 | 3 | 0 | 1 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0013 | 0/0 | 11245 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0019 | 0/0 | 11242 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0022 | 0/0 | 11243 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0023 | 0/0 | 11247 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11242): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0025 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0026 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0027 | 0/0 | 11249 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11244): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0028 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0038 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0039 | 0/0 | 11241 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11236): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0040 | 0/0 | 11243 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0041 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0042 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0043 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0044 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0046 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0047 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11239): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0048 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0051 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0052 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0053 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0054 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0055 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0056 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0057 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0058 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0059 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0060 | 0/0 | 11247 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11242): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0061 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0062 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0063 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11239): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0065 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11235): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0066 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11239): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0067 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0001c0001t0068 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0003 | 0/0 | 11235 | 56 | 14 | 9 | 32 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0010 | 0/0 | 11235 | 3 | 2 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0014 | 0/0 | 11238 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11233): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0015 | 0/0 | 11235 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0016 | 0/0 | 11241 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11236): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0017 | 0/0 | 11237 | 2 | 1 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11232): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0018 | 0/0 | 11236 | 2 | 0 | 1 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11231): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0024 | 0/0 | 11235 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0029 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11234): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0030 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0031 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0033 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0034 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11233): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0035 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
a0001c0002t0037 | 0/0 | 11237 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11232): Show |
chr11 | 77655009 | 77825722 |
a0001c0009t0036 | 0/0 | 11236 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11231): Show |
chr11 | 77655009 | 77825722 |
a0001c0010t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0001c0017t0001 | 0/0 | 11245 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0002c0003t0002 | 0/0 | 11243 | 35 | 3 | 11 | 7 | 3 | 11 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0002c0003t0008 | 0/0 | 11245 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0002c0003t0012 | 0/0 | 11245 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0002c0003t0021 | 0/0 | 11243 | 2 | 0 | 1 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0002c0003t0050 | 0/0 | 11243 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0002c0004t0002 | 0/0 | 11243 | 5 | 0 | 0 | 5 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0003c0005t0020 | 0/0 | 11243 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0003c0005t0049 | 0/0 | 11242 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0003c0016t0045 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11238): Show |
chr11 | 77655009 | 77825722 |
a0004c0006t0012 | 0/0 | 11245 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0005c0007t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0005c0007t0064 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0006c0015t0004 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11237): Show |
chr11 | 77655009 | 77825722 |
a0007c0012t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0008c0011t0007 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11235): Show |
chr11 | 77655009 | 77825722 |
a0009c0014t0005 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11240): Show |
chr11 | 77655009 | 77825722 |
a0010c0013t0007 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11235): Show |
chr11 | 77655009 | 77825722 |
a0011c0018t0032 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11235): Show |
chr11 | 77655009 | 77825722 |
a0012c0008t0003 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | AGTTC others(11230): Show |
chr11 | 77655009 | 77825722 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0013g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0019g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0019g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0022g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0023g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0023g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0025g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0026g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0027g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0028g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0038g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0039g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0040g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0041g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0042g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0043g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0044g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0046g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0047g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0048g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0051g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0052g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0053g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0054g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0055g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0056g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0057g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0058g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0059g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0060g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0061g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0062g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0063g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0065g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0066g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0067g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0001t0068g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0010g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0010g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0015g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0017g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0018g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0024g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0024g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0029g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0030g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0031g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0035g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0002t0037g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0009t0036g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0010t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0001c0017t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0008g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0012g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0021g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0021g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0003t0050g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0002c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0003c0005t0020g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0003c0005t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0003c0005t0049g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0003c0016t0045g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0004c0006t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0004c0006t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0005c0007t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0005c0007t0064g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0006c0015t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0007c0012t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0008c0011t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0009c0014t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0010c0013t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0011c0018t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
a0012c0008t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0038 | g0170 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0204 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00140 | hp1 | a0002 | c0003 | t0021 | g0209 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00280 | hp1 | a0006 | c0015 | t0004 | g0188 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0059 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0148 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00408 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00423 | hp2 | a0001 | c0002 | t0037 | g0060 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0151 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00558 | hp1 | a0007 | c0012 | t0001 | g0281 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00558 | hp2 | a0002 | c0003 | t0002 | g0303 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0162 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0205 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00673 | hp1 | a0001 | c0002 | t0030 | g0085 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00673 | hp2 | a0002 | c0004 | t0002 | g0231 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00733 | hp1 | a0002 | c0003 | t0002 | g0235 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0055 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01069 | hp1 | a0001 | c0001 | t0039 | g0166 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01070 | hp2 | a0002 | c0003 | t0002 | g0229 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0079 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01074 | hp1 | a0001 | c0002 | t0010 | g0013 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0268 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01081 | hp1 | a0001 | c0002 | t0018 | g0046 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0225 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01167 | hp2 | a0002 | c0003 | t0002 | g0238 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01168 | hp1 | a0001 | c0001 | t0053 | g0189 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01168 | hp2 | a0002 | c0003 | t0002 | g0216 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01175 | hp2 | a0001 | c0017 | t0001 | g0094 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01192 | hp1 | a0001 | c0001 | t0056 | g0159 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0052 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01243 | hp2 | a0001 | c0002 | t0017 | g0006 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01255 | hp2 | a0002 | c0003 | t0012 | g0220 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0058 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01358 | hp1 | a0001 | c0001 | t0043 | g0153 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01358 | hp2 | a0002 | c0003 | t0002 | g0228 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0056 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0236 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0269 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0080 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01515 | hp1 | a0002 | c0003 | t0002 | g0219 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0167 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01516 | hp1 | a0002 | c0003 | t0002 | g0206 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0157 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01884 | hp1 | a0001 | c0002 | t0014 | g0009 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0348 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01928 | hp1 | a0001 | c0001 | t0046 | g0171 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01928 | hp2 | a0002 | c0003 | t0002 | g0207 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0198 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0253 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01993 | hp1 | a0001 | c0001 | t0044 | g0138 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02015 | hp2 | a0002 | c0004 | t0002 | g0234 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02027 | hp2 | a0001 | c0001 | t0061 | g0306 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02040 | hp1 | a0001 | c0001 | t0067 | g0154 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02055 | hp2 | a0001 | c0002 | t0010 | g0351 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02056 | hp1 | a0001 | c0001 | t0063 | g0291 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02056 | hp2 | a0001 | c0001 | t0026 | g0256 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02071 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02074 | hp2 | a0002 | c0004 | t0002 | g0224 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02135 | hp1 | a0008 | c0011 | t0007 | g0179 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02145 | hp1 | a0001 | c0002 | t0014 | g0011 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02145 | hp2 | a0001 | c0001 | t0068 | g0352 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02148 | hp1 | a0001 | c0001 | t0011 | g0172 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0270 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02165 | hp2 | a0001 | c0001 | t0007 | g0181 | EAS | CDX | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02273 | hp2 | a0002 | c0003 | t0002 | g0214 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02280 | hp1 | a0001 | c0002 | t0034 | g0010 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02293 | hp2 | a0002 | c0003 | t0002 | g0218 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02451 | hp2 | a0003 | c0005 | t0020 | g0199 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0273 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0135 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02602 | hp2 | a0001 | c0001 | t0040 | g0116 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02615 | hp1 | a0001 | c0001 | t0054 | g0142 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0044 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02630 | hp1 | a0001 | c0001 | t0023 | g0251 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02630 | hp2 | a0001 | c0002 | t0033 | g0012 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02717 | hp2 | a0001 | c0001 | t0041 | g0249 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02809 | hp2 | a0001 | c0001 | t0052 | g0265 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02818 | hp1 | a0004 | c0006 | t0012 | g0002 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02818 | hp2 | a0003 | c0005 | t0049 | g0202 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02895 | hp1 | a0001 | c0002 | t0029 | g0017 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0242 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03017 | hp1 | a0002 | c0003 | t0002 | g0215 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03041 | hp1 | a0003 | c0005 | t0020 | g0200 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03130 | hp2 | a0001 | c0001 | t0022 | g0141 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03139 | hp1 | a0001 | c0002 | t0016 | g0008 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03195 | hp1 | a0001 | c0001 | t0023 | g0275 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03195 | hp2 | a0003 | c0016 | t0045 | g0201 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03225 | hp1 | a0001 | c0001 | t0022 | g0140 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03225 | hp2 | a0001 | c0001 | t0062 | g0283 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03239 | hp2 | a0001 | c0001 | t0028 | g0145 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03453 | hp1 | a0001 | c0009 | t0036 | g0015 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03490 | hp2 | a0002 | c0003 | t0002 | g0347 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03491 | hp2 | a0002 | c0003 | t0002 | g0222 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0345 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0221 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0232 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03688 | hp2 | a0002 | c0003 | t0002 | g0208 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03704 | hp1 | a0002 | c0003 | t0002 | g0217 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0267 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0213 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03927 | hp1 | a0002 | c0003 | t0002 | g0223 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03942 | hp1 | a0002 | c0003 | t0002 | g0346 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0178 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0164 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG04228 | hp1 | a0002 | c0003 | t0008 | g0266 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG04228 | hp2 | a0001 | c0001 | t0055 | g0144 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0067 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0271 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18939 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18942 | hp1 | a0009 | c0014 | t0005 | g0258 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18942 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18946 | hp2 | a0001 | c0001 | t0027 | g0260 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18954 | hp2 | a0001 | c0001 | t0051 | g0182 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18957 | hp1 | a0001 | c0001 | t0065 | g0146 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18963 | hp2 | a0001 | c0001 | t0019 | g0158 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18964 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18966 | hp2 | a0001 | c0001 | t0060 | g0257 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18967 | hp1 | a0001 | c0001 | t0047 | g0104 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18967 | hp2 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18969 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18971 | hp1 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18971 | hp2 | a0001 | c0001 | t0011 | g0161 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18977 | hp1 | a0001 | c0001 | t0057 | g0278 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18979 | hp1 | a0002 | c0004 | t0002 | g0237 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18981 | hp2 | a0001 | c0002 | t0015 | g0051 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18983 | hp2 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18986 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18988 | hp2 | a0005 | c0007 | t0001 | g0349 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18990 | hp1 | a0002 | c0003 | t0002 | g0212 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18991 | hp1 | a0001 | c0002 | t0035 | g0057 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18993 | hp1 | a0001 | c0001 | t0048 | g0156 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18994 | hp2 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18998 | hp2 | a0001 | c0001 | t0066 | g0173 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19005 | hp2 | a0001 | c0002 | t0024 | g0026 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19011 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0272 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19056 | hp1 | a0001 | c0002 | t0024 | g0031 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19056 | hp2 | a0005 | c0007 | t0064 | g0319 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19057 | hp1 | a0001 | c0002 | t0018 | g0065 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19062 | hp1 | a0001 | c0010 | t0001 | g0340 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19062 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19063 | hp1 | a0010 | c0013 | t0007 | g0262 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19063 | hp2 | a0001 | c0001 | t0058 | g0331 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19068 | hp2 | a0001 | c0002 | t0031 | g0075 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19074 | hp2 | a0002 | c0004 | t0002 | g0233 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19078 | hp2 | a0001 | c0002 | t0015 | g0074 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19083 | hp1 | a0001 | c0001 | t0059 | g0310 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19088 | hp1 | a0001 | c0001 | t0025 | g0259 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19088 | hp2 | a0002 | c0003 | t0050 | g0211 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19090 | hp2 | a0001 | c0001 | t0019 | g0177 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0350 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA19240 | hp2 | a0011 | c0018 | t0032 | g0014 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA20129 | hp1 | a0012 | c0008 | t0003 | g0034 | AFR | ASW | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA20129 | hp2 | a0002 | c0003 | t0002 | g0099 | AFR | ASW | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA20805 | hp1 | a0001 | c0001 | t0042 | g0174 | EUR | TSI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01123 | hp1 | a0002 | c0003 | t0021 | g0210 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02486 | hp1 | a0002 | c0003 | t0002 | g0227 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG02559 | hp2 | a0001 | c0002 | t0016 | g0005 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03471 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG06807 | hp1 | a0004 | c0006 | t0012 | g0001 | AFR | USA | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
HG06807 | hp2 | a0001 | c0002 | t0017 | g0007 | AFR | USA | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18955 | hp1 | a0002 | c0003 | t0002 | g0203 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0096 | REF | REF | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0226 | REF | REF | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:77667286 | A | C | 1 | a0008 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.3957T>G | p.Asn1319Lys | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3965/11242 | 3957/4326 | 1319/1441 | chr11 | 77667286 | |||
chr11:77667329 | G | A | 1 | a0007 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.3914C>T | p.Thr1305Met | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3922/11242 | 3914/4326 | 1305/1441 | chr11 | 77667329 | |||
chr11:77675080 | T | G | 1 | a0010 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.3518A>C | p.Asp1173Ala | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/16 | 3526/11242 | 3518/4326 | 1173/1441 | chr11 | 77675080 | |||
chr11:77676888 | G | C | 1 | a0012 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.3245C>G | p.Ala1082Gly | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/16 | 3253/11242 | 3245/4326 | 1082/1441 | chr11 | 77676888 | |||
chr11:77701117 | G | T | 1 | a0012 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2112C>A | p.Ser704Arg | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2120/11242 | 2112/4326 | 704/1441 | chr11 | 77701117 | |||
chr11:77701134 | C | G | 1 | a0005 | 2 | NA18988.hp2 NA19056.hp2 |
missense_variant | MODERATE | c.2095G>C | p.Gly699Arg | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2103/11242 | 2095/4326 | 699/1441 | chr11 | 77701134 | |||
chr11:77701197 | C | A | 1 | a0009 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2032G>T | p.Val678Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2040/11242 | 2032/4326 | 678/1441 | chr11 | 77701197 | |||
chr11:77701411 | T | C | 1 | a0006 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1818A>G | p.Ile606Met | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1826/11242 | 1818/4326 | 606/1441 | chr11 | 77701411 | |||
chr11:77701806 | A | C | 1 | a0002 | 5 | HG00673.hp2 HG02015.hp2 HG02074.hp2 others(2): Show |
missense_variant | MODERATE | c.1423T>G | p.Ser475Ala | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1431/11242 | 1423/4326 | 475/1441 | chr11 | 77701806 | |||
chr11:77701806 | A | G | 1 | a0002 | 40 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(37): Show |
missense_variant | MODERATE | c.1423T>C | p.Ser475Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1431/11242 | 1423/4326 | 475/1441 | chr11 | 77701806 | |||
chr11:77702178 | T | C | 1 | a0003 | 4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.1051A>G | p.Ile351Val | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1059/11242 | 1051/4326 | 351/1441 | chr11 | 77702178 | |||
chr11:77702317 | T | G | 1 | a0011 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.912A>C | p.Glu304Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 920/11242 | 912/4326 | 304/1441 | chr11 | 77702317 | |||
chr11:77820687 | C | G | 1 | a0004 | 2 | HG02818.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.28G>C | p.Val10Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/16 | 36/11242 | 28/4326 | 10/1441 | chr11 | 77820687 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:77667343 | T | C | 4 | a0001c0002 a0001c0009 a0011c0018 others(1): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.3900A>G | p.Leu1300Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3908/11242 | 3900/4326 | 1300/1441 | chr11 | 77667343 | |||
chr11:77667460 | A | G | 4 | a0001c0002 a0001c0009 a0011c0018 others(1): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.3783T>C | p.Asp1261Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3791/11242 | 3783/4326 | 1261/1441 | chr11 | 77667460 | |||
chr11:77672205 | A | G | 1 | a0003c0016 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3588T>C | p.Ser1196Ser | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/16 | 3596/11242 | 3588/4326 | 1196/1441 | chr11 | 77672205 | |||
chr11:77698523 | T | C | 4 | a0001c0002 a0001c0009 a0011c0018 others(1): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.2679A>G | p.Pro893Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/16 | 2687/11242 | 2679/4326 | 893/1441 | chr11 | 77698523 | |||
chr11:77698622 | A | G | 1 | a0001c0010 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.2580T>C | p.Asp860Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/16 | 2588/11242 | 2580/4326 | 860/1441 | chr11 | 77698622 | |||
chr11:77700931 | C | T | 1 | a0001c0009 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2298G>A | p.Glu766Glu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2306/11242 | 2298/4326 | 766/1441 | chr11 | 77700931 | |||
chr11:77702266 | G | C | 1 | a0001c0017 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.963C>G | p.Pro321Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 971/11242 | 963/4326 | 321/1441 | chr11 | 77702266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:77660021 | T | C | 1 | a0001c0002t0017 | 2 | HG01243.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6896A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6896 | chr11 | 77660021 | ||||||
chr11:77660030 | T | C | 2 | a0001c0001t0059 a0001c0001t0060 |
2 | NA18966.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6887A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6887 | chr11 | 77660030 | ||||||
chr11:77660169 | G | C | 1 | a0001c0002t0033 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6748C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6748 | chr11 | 77660169 | ||||||
chr11:77660386 | T | C | 1 | a0001c0001t0046 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6531A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6531 | chr11 | 77660386 | ||||||
chr11:77660449 | G | C | 18 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0014 others(15): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*6468C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6468 | chr11 | 77660449 | ||||||
chr11:77660581 | T | C | 2 | a0001c0001t0059 a0001c0001t0060 |
2 | NA18966.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6336A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6336 | chr11 | 77660581 | ||||||
chr11:77660708 | C | G | 1 | a0011c0018t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6209G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6209 | chr11 | 77660708 | ||||||
chr11:77660749 | G | T | 1 | a0003c0005t0049 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6168C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6168 | chr11 | 77660749 | ||||||
chr11:77660775 | T | C | 1 | a0001c0002t0035 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6142A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6142 | chr11 | 77660775 | ||||||
chr11:77660800 | AC | A | 17 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0014 others(14): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*6116delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6116 | chr11 | 77660800 | ||||||
chr11:77661120 | A | C | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0013 others(7): Show |
23 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5797T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5797 | chr11 | 77661120 | ||||||
chr11:77661187 | C | G | 2 | a0001c0002t0014 a0001c0002t0034 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5730G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5730 | chr11 | 77661187 | ||||||
chr11:77661204 | T | C | 1 | a0011c0018t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5713A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5713 | chr11 | 77661204 | ||||||
chr11:77661311 | T | A | 1 | a0002c0003t0050 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5606A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5606 | chr11 | 77661311 | ||||||
chr11:77661376 | GC | G | 9 | a0001c0002t0003 a0001c0002t0015 a0001c0002t0018 others(6): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5540delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5540 | chr11 | 77661376 | ||||||
chr11:77661437 | A | ATG | 11 | a0001c0001t0023 a0001c0001t0041 a0001c0001t0047 others(8): Show |
14 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5478_*5479dupCA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5479 | chr11 | 77661437 | ||||||
chr11:77661437 | A | ATGTG | 2 | a0001c0001t0027 a0001c0002t0016 |
3 | HG02559.hp2 HG03139.hp1 NA18946.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5476_*5479dupCACA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5479 | chr11 | 77661437 | ||||||
chr11:77661437 | ATG | A | 3 | a0001c0001t0052 a0001c0002t0010 a0001c0002t0033 |
5 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5478_*5479delCA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5478 | chr11 | 77661437 | ||||||
chr11:77661464 | C | T | 1 | a0001c0001t0025 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5453G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5453 | chr11 | 77661464 | ||||||
chr11:77661638 | T | C | 1 | a0001c0001t0062 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5279A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5279 | chr11 | 77661638 | ||||||
chr11:77661673 | T | C | 1 | a0001c0001t0048 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5244A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5244 | chr11 | 77661673 | ||||||
chr11:77661727 | T | G | 1 | a0001c0001t0026 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5190A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5190 | chr11 | 77661727 | ||||||
chr11:77661733 | A | T | 2 | a0001c0001t0019 a0011c0018t0032 |
3 | NA18963.hp2 NA19090.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5184T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5184 | chr11 | 77661733 | ||||||
chr11:77661762 | CT | C | 10 | a0001c0001t0039 a0001c0001t0063 a0001c0002t0010 others(7): Show |
15 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5154delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5154 | chr11 | 77661762 | ||||||
chr11:77661762 | CTT | C | 11 | a0001c0002t0003 a0001c0002t0014 a0001c0002t0015 others(8): Show |
69 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5153_*5154delAA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5153 | chr11 | 77661762 | ||||||
chr11:77662028 | C | T | 1 | a0001c0001t0059 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4889G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4889 | chr11 | 77662028 | ||||||
chr11:77662037 | T | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4880A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4880 | chr11 | 77662037 | ||||||
chr11:77662157 | C | T | 1 | a0001c0001t0022 | 2 | HG03130.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4760G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4760 | chr11 | 77662157 | ||||||
chr11:77662205 | T | C | 2 | a0001c0001t0013 a0001c0001t0052 |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4712A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4712 | chr11 | 77662205 | ||||||
chr11:77662327 | G | T | 3 | a0001c0001t0011 a0001c0001t0046 a0001c0001t0056 |
5 | HG01192.hp1 HG01928.hp1 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4590C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4590 | chr11 | 77662327 | ||||||
chr11:77662369 | T | G | 12 | a0001c0002t0003 a0001c0002t0014 a0001c0002t0015 others(9): Show |
71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*4548A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4548 | chr11 | 77662369 | ||||||
chr11:77662426 | C | A | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(49): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*4491G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4491 | chr11 | 77662426 | ||||||
chr11:77662543 | A | G | 2 | a0001c0002t0016 a0001c0002t0017 |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4374T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4374 | chr11 | 77662543 | ||||||
chr11:77662584 | T | TA | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(54): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*4332dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4332 | chr11 | 77662584 | ||||||
chr11:77662685 | C | A | 1 | a0001c0001t0065 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4232G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4232 | chr11 | 77662685 | ||||||
chr11:77662864 | T | C | 1 | a0002c0003t0021 | 2 | HG00140.hp1 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4053A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4053 | chr11 | 77662864 | ||||||
chr11:77662888 | G | A | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0025 others(4): Show |
18 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4029C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4029 | chr11 | 77662888 | ||||||
chr11:77663004 | G | A | 1 | a0001c0001t0051 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3913 | chr11 | 77663004 | ||||||
chr11:77663017 | G | T | 1 | a0001c0002t0015 | 2 | NA18981.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3900C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3900 | chr11 | 77663017 | ||||||
chr11:77663019 | G | GCA | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(21): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3896_*3897dupTG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3897 | chr11 | 77663019 | ||||||
chr11:77663097 | A | G | 1 | a0003c0016t0045 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3820T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3820 | chr11 | 77663097 | ||||||
chr11:77663164 | A | G | 1 | a0001c0001t0044 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3753T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3753 | chr11 | 77663164 | ||||||
chr11:77663356 | A | C | 2 | a0001c0001t0028 a0001c0001t0043 |
2 | HG01358.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3561T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3561 | chr11 | 77663356 | ||||||
chr11:77663385 | T | A | 1 | a0001c0001t0009 | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3532A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3532 | chr11 | 77663385 | ||||||
chr11:77663406 | A | G | 1 | a0001c0001t0042 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3511T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3511 | chr11 | 77663406 | ||||||
chr11:77663626 | T | A | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3291A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3291 | chr11 | 77663626 | ||||||
chr11:77663709 | A | T | 1 | a0001c0001t0058 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3208T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3208 | chr11 | 77663709 | ||||||
chr11:77663989 | T | C | 1 | a0001c0001t0053 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2928A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2928 | chr11 | 77663989 | ||||||
chr11:77664037 | C | T | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2880G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2880 | chr11 | 77664037 | ||||||
chr11:77664181 | A | G | 1 | a0001c0002t0031 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2736T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2736 | chr11 | 77664181 | ||||||
chr11:77664316 | G | A | 1 | a0001c0001t0027 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2601C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2601 | chr11 | 77664316 | ||||||
chr11:77664525 | C | T | 1 | a0001c0002t0030 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2392G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2392 | chr11 | 77664525 | ||||||
chr11:77664738 | T | C | 2 | a0001c0001t0022 a0001c0001t0054 |
3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2179A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2179 | chr11 | 77664738 | ||||||
chr11:77664752 | T | C | 1 | a0001c0001t0055 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2165A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2165 | chr11 | 77664752 | ||||||
chr11:77664886 | T | G | 1 | a0001c0001t0056 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2031A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2031 | chr11 | 77664886 | ||||||
chr11:77665060 | A | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1857T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1857 | chr11 | 77665060 | ||||||
chr11:77665065 | A | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1852T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1852 | chr11 | 77665065 | ||||||
chr11:77665078 | A | G | 1 | a0001c0001t0057 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1839T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1839 | chr11 | 77665078 | ||||||
chr11:77665163 | G | T | 2 | a0001c0001t0006 a0001c0001t0041 |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1754C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1754 | chr11 | 77665163 | ||||||
chr11:77665202 | C | T | 18 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0014 others(15): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1715G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1715 | chr11 | 77665202 | ||||||
chr11:77665369 | A | G | 1 | a0001c0001t0040 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1548T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1548 | chr11 | 77665369 | ||||||
chr11:77665432 | T | C | 1 | a0005c0007t0064 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1485A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1485 | chr11 | 77665432 | ||||||
chr11:77665733 | A | G | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG00099.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1184T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1184 | chr11 | 77665733 | ||||||
chr11:77665761 | C | A | 15 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0057 others(12): Show |
85 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1156 | chr11 | 77665761 | ||||||
chr11:77665776 | GCACA | G | 18 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0014 others(15): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1137_*1140delTGTG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1137 | chr11 | 77665776 | ||||||
chr11:77665787 | AAC | A | 4 | a0001c0001t0007 a0001c0001t0065 a0008c0011t0007 others(1): Show |
7 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1128_*1129delGT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1128 | chr11 | 77665787 | ||||||
chr11:77665799 | C | T | 1 | a0001c0002t0014 | 2 | HG01884.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1118G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1118 | chr11 | 77665799 | ||||||
chr11:77665873 | G | A | 1 | a0001c0002t0024 | 2 | NA19005.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1044C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1044 | chr11 | 77665873 | ||||||
chr11:77666247 | A | T | 1 | a0001c0001t0028 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 670 | chr11 | 77666247 | ||||||
chr11:77666373 | G | C | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | HG02040.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*544C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 544 | chr11 | 77666373 | ||||||
chr11:77666756 | C | A | 1 | a0001c0001t0068 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 161 | chr11 | 77666756 | ||||||
chr11:77666823 | A | T | 5 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0026 others(2): Show |
13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*94T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 94 | chr11 | 77666823 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:77667518 | T | C | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3752-27A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667518 | |||||||
chr11:77667636 | T | C | 1 | a0005c0007t0001g0349 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3752-145A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667636 | |||||||
chr11:77667760 | A | G | 76 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.3752-269T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667760 | |||||||
chr11:77667841 | T | A | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3752-350A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667841 | |||||||
chr11:77667849 | G | A | 45 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3752-358C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667849 | |||||||
chr11:77667862 | C | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3752-371G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667862 | |||||||
chr11:77668054 | A | G | 272 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(269): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.3752-563T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668054 | |||||||
chr11:77668160 | C | T | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3752-669G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668160 | |||||||
chr11:77668255 | G | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3752-764C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668255 | |||||||
chr11:77668262 | A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3752-771T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668262 | |||||||
chr11:77668311 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3752-820A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668311 | |||||||
chr11:77668370 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3752-879A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668370 | |||||||
chr11:77668517 | T | C | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3752-1026A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668517 | |||||||
chr11:77668543 | T | G | 67 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3752-1052A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668543 | |||||||
chr11:77668595 | A | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3752-1104T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668595 | |||||||
chr11:77668713 | G | T | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.3752-1222C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668713 | |||||||
chr11:77668807 | C | A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3752-1316G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668807 | |||||||
chr11:77668921 | C | CAT | 349 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(346): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.3752-1432_3752-143 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668921 | |||||||
chr11:77669033 | C | T | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3752-1542G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669033 | |||||||
chr11:77669103 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3752-1612G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669103 | |||||||
chr11:77669183 | T | C | 1 | a0002c0003t0002g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3752-1692A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669183 | |||||||
chr11:77669189 | C | T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3752-1698G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669189 | |||||||
chr11:77669448 | T | C | 67 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3752-1957A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669448 | |||||||
chr11:77669820 | A | G | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3751+2222T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669820 | |||||||
chr11:77669989 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+2053A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669989 | |||||||
chr11:77670092 | C | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(28): Show |
31 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.3751+1950G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670092 | |||||||
chr11:77670350 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0290 a0001c0001t0001g0308 |
3 | HG01891.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3751+1692G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670350 | |||||||
chr11:77670427 | G | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3751+1615C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670427 | |||||||
chr11:77670539 | C | T | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0126 |
3 | NA18963.hp1 NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3751+1503G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670539 | |||||||
chr11:77670706 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.3751+1336A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670706 | |||||||
chr11:77670721 | T | A | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0117 |
3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3751+1321A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670721 | |||||||
chr11:77670844 | C | T | 3 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 |
3 | HG02083.hp2 NA18612.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3751+1198G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670844 | |||||||
chr11:77670913 | C | T | 107 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(104): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.3751+1129G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670913 | |||||||
chr11:77671021 | G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+1021C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671021 | |||||||
chr11:77671106 | C | CA | 8 | a0001c0001t0001g0309 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00280.hp1 HG02145.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.3751+935dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671106 | |||||||
chr11:77671106 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0008g0267 a0001c0001t0008g0270 |
2 | HG02148.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3751+921_3751+935d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671106 | |||||||
chr11:77671122 | AAAAAAAA others(25): Show |
A | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3751+888_3751+919d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671122 | |||||||
chr11:77671122 | AAAAAAAA others(27): Show |
A | 11 | a0001c0002t0003g0018 a0001c0002t0003g0022 a0001c0002t0003g0023 others(8): Show |
11 | HG01243.hp2 HG02132.hp1 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.3751+886_3751+919d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671122 | |||||||
chr11:77671123 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0002g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3751+894_3751+918d others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | |||||||
chr11:77671123 | AAAAAAAA others(26): Show |
A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3751+886_3751+918d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | |||||||
chr11:77671123 | AAAAAAAA others(28): Show |
A | 1 | a0001c0002t0003g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3751+884_3751+918d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | |||||||
chr11:77671124 | AAAAAAAA others(23): Show |
A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+888_3751+917d others(32): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | |||||||
chr11:77671124 | AAAAAAAA others(25): Show |
A | 2 | a0001c0002t0003g0030 a0001c0002t0003g0072 |
2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3751+886_3751+917d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | |||||||
chr11:77671124 | AAAAAAAA others(27): Show |
A | 34 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 others(31): Show |
34 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3751+884_3751+917d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | |||||||
chr11:77671125 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0008g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3751+900_3751+916d others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | |||||||
chr11:77671125 | AAAAAAAA others(26): Show |
A | 3 | a0001c0002t0003g0052 a0001c0002t0003g0061 a0001c0002t0003g0063 |
3 | HG00597.hp1 HG01192.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.3751+884_3751+916d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | |||||||
chr11:77671125 | AAAAAAAA others(28): Show |
A | 3 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0018g0046 |
3 | HG01074.hp1 HG01081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3751+882_3751+916d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | |||||||
chr11:77671126 | AAAAAAAA others(25): Show |
A | 1 | a0001c0002t0003g0073 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3751+884_3751+915d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671126 | |||||||
chr11:77671126 | AAAAAAAA others(27): Show |
A | 18 | a0001c0002t0003g0033 a0001c0002t0003g0037 a0001c0002t0003g0039 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3751+882_3751+915d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671126 | |||||||
chr11:77671127 | AAAAAAAA others(26): Show |
A | 3 | a0001c0002t0003g0032 a0001c0002t0003g0036 a0001c0002t0003g0069 |
3 | HG02809.hp1 HG03579.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.3751+882_3751+914d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671127 | |||||||
chr11:77671127 | AAAAAAAA others(28): Show |
A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3751+880_3751+914d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671127 | |||||||
chr11:77671129 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3751+898_3751+912d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671129 | |||||||
chr11:77671134 | AAAAAATA others(3): Show |
A | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3751+898_3751+907d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671134 | |||||||
chr11:77671136 | A | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG02818.hp1 HG03516.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.3751+906T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671136 | |||||||
chr11:77671136 | AAAATATA others(9): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3751+890_3751+905d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671136 | |||||||
chr11:77671137 | AAATATAT others(4): Show |
A | 2 | a0001c0001t0022g0141 a0001c0001t0054g0142 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3751+894_3751+904d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671137 | |||||||
chr11:77671137 | AAATATAT others(16): Show |
A | 2 | a0001c0001t0053g0189 a0010c0013t0007g0262 |
2 | HG01168.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3751+882_3751+904d others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671137 | |||||||
chr11:77671138 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3751+903_3751+904i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | A | AT | 3 | a0001c0001t0005g0253 a0001c0001t0038g0170 a0009c0014t0005g0258 |
3 | HG00099.hp1 HG01975.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.3751+903_3751+904i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | A | T | 19 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0092 others(16): Show |
19 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.3751+904T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AAT | A | 17 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0001t0002g0129 others(14): Show |
17 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.3751+902_3751+903d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATAT | A | 17 | a0001c0001t0001g0093 a0001c0001t0001g0301 a0001c0001t0002g0124 others(14): Show |
17 | HG00558.hp2 HG00639.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3751+900_3751+903d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATAT | A | 18 | a0001c0001t0001g0280 a0001c0001t0001g0312 a0001c0001t0001g0334 others(15): Show |
18 | HG00099.hp2 HG00673.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.3751+898_3751+903d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(1): Show |
A | 16 | a0001c0001t0001g0292 a0001c0001t0001g0307 a0001c0001t0001g0311 others(13): Show |
16 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.3751+896_3751+903d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(3): Show |
A | 11 | a0001c0001t0001g0279 a0001c0001t0001g0295 a0001c0001t0001g0296 others(8): Show |
11 | HG00423.hp1 HG00544.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.3751+894_3751+903d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(5): Show |
A | 2 | a0003c0005t0020g0200 a0008c0011t0007g0179 |
2 | HG02135.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3751+892_3751+903d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(7): Show |
A | 1 | a0001c0001t0002g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3751+890_3751+903d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(9): Show |
A | 1 | a0001c0001t0002g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3751+888_3751+903d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3751+884_3751+903d others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671138 | AATATATA others(15): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3751+882_3751+903d others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | |||||||
chr11:77671139 | AT | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0285 a0001c0001t0002g0003 others(6): Show |
9 | HG00323.hp2 HG01109.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3751+902delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATAT | A | 17 | a0001c0001t0002g0132 a0001c0001t0004g0137 a0001c0001t0004g0150 others(14): Show |
17 | HG00733.hp1 HG01167.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.3751+900_3751+902d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATATAT | A | 18 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0002g0108 others(15): Show |
18 | HG00741.hp2 HG01070.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.3751+898_3751+902d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATATATAT | A | 8 | a0001c0001t0001g0282 a0001c0001t0001g0286 a0001c0001t0001g0288 others(5): Show |
8 | HG00140.hp2 HG02132.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.3751+896_3751+902d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATATATAT others(2): Show |
A | 8 | a0001c0001t0001g0274 a0001c0001t0001g0287 a0001c0001t0001g0290 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.3751+894_3751+902d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATATATAT others(4): Show |
A | 5 | a0001c0001t0001g0276 a0001c0001t0058g0331 a0001c0001t0063g0291 others(2): Show |
5 | HG00558.hp1 HG02056.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3751+892_3751+902d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671139 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3751+884_3751+902d others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | |||||||
chr11:77671140 | T | A | 12 | a0001c0001t0001g0298 a0001c0001t0001g0322 a0001c0001t0001g0323 others(9): Show |
12 | HG00280.hp1 HG01123.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.3751+902A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671140 | |||||||
chr11:77671142 | T | A | 21 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0001t0002g0003 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.3751+900A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671142 | |||||||
chr11:77671144 | T | A | 34 | a0001c0001t0001g0093 a0001c0001t0001g0301 a0001c0001t0002g0129 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3751+898A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671144 | |||||||
chr11:77671146 | T | A | 35 | a0001c0001t0001g0280 a0001c0001t0001g0312 a0001c0001t0001g0334 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.3751+896A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671146 | |||||||
chr11:77671148 | T | A | 29 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0286 others(26): Show |
29 | HG00408.hp1 HG00609.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.3751+894A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671148 | |||||||
chr11:77671150 | T | A | 24 | a0001c0001t0001g0279 a0001c0001t0001g0290 a0001c0001t0001g0295 others(21): Show |
24 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.3751+892A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671150 | |||||||
chr11:77671152 | T | A | 8 | a0001c0001t0001g0276 a0001c0001t0001g0290 a0001c0001t0006g0123 others(5): Show |
8 | HG01891.hp2 HG02056.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3751+890A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671152 | |||||||
chr11:77671154 | T | A | 2 | a0001c0001t0002g0117 a0001c0001t0041g0249 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3751+888A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671154 | |||||||
chr11:77671156 | T | A | 1 | a0001c0001t0002g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3751+886A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671156 | |||||||
chr11:77671160 | T | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3751+882A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671160 | |||||||
chr11:77671199 | A | G | 5 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0290 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3751+843T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671199 | |||||||
chr11:77671208 | T | TATAC | 12 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(9): Show |
12 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.3751+833_3751+834i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671208 | |||||||
chr11:77671208 | T | TATATAC | 68 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3751+833_3751+834i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671208 | |||||||
chr11:77671241 | A | G | 2 | a0002c0003t0002g0208 a0002c0003t0002g0227 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3751+801T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671241 | |||||||
chr11:77671318 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3751+724A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671318 | |||||||
chr11:77671402 | T | C | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3751+640A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671402 | |||||||
chr11:77671634 | AT | A | 257 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(254): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.3751+407delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671634 | |||||||
chr11:77671782 | G | A | 24 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(21): Show |
24 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.3751+260C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671782 | |||||||
chr11:77671842 | C | T | 1 | a0002c0003t0002g0218 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3751+200G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671842 | |||||||
chr11:77672019 | T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3751+23A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77672019 | |||||||
chr11:77672307 | A | G | 1 | a0002c0003t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3563-77T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672307 | |||||||
chr11:77672379 | G | C | 68 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3563-149C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672379 | |||||||
chr11:77672466 | T | C | 269 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(266): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.3563-236A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672466 | |||||||
chr11:77672579 | TA | T | 82 | a0001c0001t0004g0148 a0001c0002t0003g0018 a0001c0002t0003g0019 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3563-350delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672579 | |||||||
chr11:77672594 | T | C | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3563-364A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672594 | |||||||
chr11:77672685 | T | C | 1 | a0002c0004t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3563-455A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672685 | |||||||
chr11:77672716 | T | G | 1 | a0001c0001t0004g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3563-486A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672716 | |||||||
chr11:77672721 | C | T | 1 | a0001c0001t0027g0260 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3563-491G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672721 | |||||||
chr11:77672722 | G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3563-492C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672722 | |||||||
chr11:77672807 | C | T | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3563-577G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672807 | |||||||
chr11:77672924 | C | T | 1 | a0002c0004t0002g0233 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3563-694G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672924 | |||||||
chr11:77673127 | C | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3563-897G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673127 | |||||||
chr11:77673194 | T | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3563-964A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673194 | |||||||
chr11:77673392 | C | T | 4 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3563-1162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673392 | |||||||
chr11:77673673 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3562+1363T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673673 | |||||||
chr11:77673926 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3562+1110A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673926 | |||||||
chr11:77673951 | C | T | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3562+1085G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673951 | |||||||
chr11:77673963 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3562+1073C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673963 | |||||||
chr11:77674023 | T | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3562+1013A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674023 | |||||||
chr11:77674217 | A | C | 1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3562+819T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674217 | |||||||
chr11:77674666 | G | A | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+370C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674666 | |||||||
chr11:77674667 | A | G | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+369T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674667 | |||||||
chr11:77674789 | C | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3562+247G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674789 | |||||||
chr11:77674868 | A | G | 269 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(266): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.3562+168T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674868 | |||||||
chr11:77674895 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3562+141T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674895 | |||||||
chr11:77674923 | C | G | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+113G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674923 | |||||||
chr11:77674923 | C | T | 67 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3562+113G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674923 | |||||||
chr11:77674924 | G | C | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+112C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674924 | |||||||
chr11:77674979 | A | G | 1 | a0001c0002t0003g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3562+57T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674979 | |||||||
chr11:77675003 | T | C | 1 | a0001c0001t0004g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3562+33A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675003 | |||||||
chr11:77675004 | T | G | 1 | a0001c0001t0004g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3562+32A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675004 | |||||||
chr11:77675027 | T | G | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3562+9A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675027 | |||||||
chr11:77675618 | C | T | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3342-362G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675618 | |||||||
chr11:77675913 | A | G | 1 | a0001c0001t0048g0156 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3342-657T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675913 | |||||||
chr11:77675978 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3342-722G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675978 | |||||||
chr11:77676279 | CT | C | 6 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0312 others(3): Show |
6 | HG01069.hp1 HG02451.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.3341+512delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676279 | |||||||
chr11:77676279 | CTT | C | 80 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3341+511_3341+512d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676279 | |||||||
chr11:77676309 | G | C | 1 | a0001c0001t0063g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3341+483C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676309 | |||||||
chr11:77676424 | C | T | 1 | a0001c0002t0003g0028 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3341+368G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676424 | |||||||
chr11:77676489 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3341+303G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676489 | |||||||
chr11:77676747 | T | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3341+45A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676747 | |||||||
chr11:77676768 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3341+24C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676768 | |||||||
chr11:77677083 | T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3134-84A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677083 | |||||||
chr11:77677252 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3134-253C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677252 | |||||||
chr11:77677316 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3134-317G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677316 | |||||||
chr11:77677599 | T | C | 1 | a0001c0001t0062g0283 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3133+487A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677599 | |||||||
chr11:77677703 | G | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3133+383C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677703 | |||||||
chr11:77677800 | G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3133+286C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677800 | |||||||
chr11:77677975 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.3133+111A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677975 | |||||||
chr11:77677988 | G | A | 1 | a0001c0001t0011g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3133+98C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677988 | |||||||
chr11:77678007 | T | C | 1 | a0001c0001t0001g0328 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3133+79A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77678007 | |||||||
chr11:77678193 | CT | C | 160 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(157): Show |
160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.3066-41delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | |||||||
chr11:77678193 | CTT | C | 183 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.3066-42_3066-41del others(2): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | |||||||
chr11:77678193 | CTTT | C | 6 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0312 others(3): Show |
6 | HG01070.hp2 HG02027.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066-43_3066-41del others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | |||||||
chr11:77678228 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3066-75A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678228 | |||||||
chr11:77678240 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3066-87G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678240 | |||||||
chr11:77678419 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3066-266C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678419 | |||||||
chr11:77678506 | C | T | 1 | a0002c0003t0002g0241 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3066-353G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678506 | |||||||
chr11:77678610 | G | C | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3066-457C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678610 | |||||||
chr11:77678724 | T | C | 2 | a0002c0003t0002g0099 a0002c0003t0002g0228 |
2 | HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3066-571A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678724 | |||||||
chr11:77678812 | A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3066-659T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678812 | |||||||
chr11:77678925 | C | T | 1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3066-772G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678925 | |||||||
chr11:77679089 | C | CA | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3066-937dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679089 | |||||||
chr11:77679257 | T | C | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0051g0182 |
3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3066-1104A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679257 | |||||||
chr11:77679586 | T | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3066-1433A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679586 | |||||||
chr11:77679606 | G | C | 2 | a0001c0001t0019g0158 a0001c0001t0019g0177 |
2 | NA18963.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3066-1453C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679606 | |||||||
chr11:77679613 | A | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3066-1460T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679613 | |||||||
chr11:77679659 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3066-1506G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679659 | |||||||
chr11:77679672 | C | CA | 38 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0002g0003 others(35): Show |
38 | HG00639.hp2 HG01516.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.3066-1520dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679672 | |||||||
chr11:77680060 | T | C | 1 | a0001c0001t0042g0174 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3066-1907A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680060 | |||||||
chr11:77680121 | G | A | 4 | a0001c0001t0013g0271 a0001c0001t0013g0272 a0001c0001t0013g0273 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3066-1968C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680121 | |||||||
chr11:77680162 | A | G | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.3066-2009T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680162 | |||||||
chr11:77680639 | C | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3066-2486G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680639 | |||||||
chr11:77680650 | T | C | 3 | a0001c0001t0001g0279 a0005c0007t0001g0349 a0005c0007t0064g0319 |
3 | NA18988.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3066-2497A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680650 | |||||||
chr11:77680727 | A | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3066-2574T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680727 | |||||||
chr11:77680759 | A | G | 4 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | NA18968.hp2 NA18979.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.3066-2606T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680759 | |||||||
chr11:77680993 | A | C | 1 | a0001c0001t0001g0335 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3065+2717T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680993 | |||||||
chr11:77681011 | A | C | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3065+2699T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681011 | |||||||
chr11:77681094 | C | T | 13 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(10): Show |
13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.3065+2616G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681094 | |||||||
chr11:77681121 | T | G | 1 | a0003c0005t0020g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3065+2589A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681121 | |||||||
chr11:77681150 | T | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3065+2560A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681150 | |||||||
chr11:77681258 | G | A | 1 | a0001c0002t0037g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3065+2452C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681258 | |||||||
chr11:77681499 | T | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3065+2211A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681499 | |||||||
chr11:77682059 | T | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3065+1651A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682059 | |||||||
chr11:77682093 | T | G | 3 | a0001c0001t0001g0279 a0005c0007t0001g0349 a0005c0007t0064g0319 |
3 | NA18988.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3065+1617A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682093 | |||||||
chr11:77682311 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3065+1399C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682311 | |||||||
chr11:77682354 | T | G | 4 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065+1356A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682354 | |||||||
chr11:77682495 | G | A | 9 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(6): Show |
9 | HG01074.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3065+1215C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682495 | |||||||
chr11:77682649 | C | T | 1 | a0002c0003t0002g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3065+1061G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682649 | |||||||
chr11:77682673 | C | T | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3065+1037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682673 | |||||||
chr11:77682714 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3065+996C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682714 | |||||||
chr11:77682873 | AGCATGT | A | 4 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065+831_3065+836d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682873 | |||||||
chr11:77682901 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3065+809C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682901 | |||||||
chr11:77682948 | G | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3065+762C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682948 | |||||||
chr11:77683026 | C | T | 6 | a0002c0003t0002g0207 a0002c0003t0002g0225 a0002c0003t0002g0345 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.3065+684G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683026 | |||||||
chr11:77683173 | C | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3065+537G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683173 | |||||||
chr11:77683228 | T | C | 1 | a0002c0003t0002g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3065+482A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683228 | |||||||
chr11:77683397 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3065+313T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683397 | |||||||
chr11:77683426 | G | A | 1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3065+284C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683426 | |||||||
chr11:77683532 | C | T | 9 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(6): Show |
9 | HG01074.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3065+178G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683532 | |||||||
chr11:77683555 | G | A | 159 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.3065+155C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683555 | |||||||
chr11:77683556 | G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3065+154C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683556 | |||||||
chr11:77683859 | T | C | 1 | a0001c0001t0009g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2956-40A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77683859 | |||||||
chr11:77684207 | T | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2956-388A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684207 | |||||||
chr11:77684324 | A | G | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2956-505T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684324 | |||||||
chr11:77684429 | C | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0289 |
2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2956-610G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684429 | |||||||
chr11:77684652 | G | A | 67 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2955+453C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684652 | |||||||
chr11:77684736 | C | G | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2955+369G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684736 | |||||||
chr11:77684790 | C | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+315G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684790 | |||||||
chr11:77684804 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2955+301T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684804 | |||||||
chr11:77684822 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+283A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684822 | |||||||
chr11:77684844 | C | T | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2955+261G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684844 | |||||||
chr11:77684988 | G | GAAAT | 9 | a0001c0001t0002g0120 a0001c0001t0004g0152 a0001c0001t0007g0162 others(6): Show |
9 | HG00597.hp2 HG01074.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+113_2955+116d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | |||||||
chr11:77684988 | G | GAAATAAA others(1): Show |
59 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(56): Show |
59 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2955+109_2955+116d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | |||||||
chr11:77684988 | G | GAAATAAA others(5): Show |
13 | a0001c0002t0003g0022 a0001c0002t0003g0027 a0001c0002t0003g0028 others(10): Show |
13 | HG00423.hp2 HG00733.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2955+105_2955+116d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | |||||||
chr11:77684988 | G | GAAATAAA others(9): Show |
4 | a0001c0002t0003g0032 a0001c0002t0016g0005 a0001c0002t0016g0008 others(1): Show |
4 | HG02559.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+101_2955+116d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | |||||||
chr11:77685294 | A | ATTAT | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2901-139_2901-136d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685294 | |||||||
chr11:77685295 | T | C | 1 | a0001c0002t0003g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2901-136A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685295 | |||||||
chr11:77685356 | C | T | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2901-197G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685356 | |||||||
chr11:77685676 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0004g0186 |
2 | HG00140.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2901-517T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685676 | |||||||
chr11:77685695 | T | C | 1 | a0001c0001t0004g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2901-536A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685695 | |||||||
chr11:77685813 | T | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2901-654A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685813 | |||||||
chr11:77685843 | T | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-684A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685843 | |||||||
chr11:77686014 | A | G | 80 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2901-855T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686014 | |||||||
chr11:77686068 | A | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-909T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686068 | |||||||
chr11:77686120 | T | C | 1 | a0001c0002t0018g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2901-961A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686120 | |||||||
chr11:77686141 | T | G | 2 | a0002c0003t0002g0221 a0002c0003t0002g0229 |
2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2901-982A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686141 | |||||||
chr11:77686163 | T | C | 1 | a0001c0001t0004g0198 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2901-1004A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686163 | |||||||
chr11:77686234 | T | C | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2901-1075A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686234 | |||||||
chr11:77686408 | C | CAAAAA | 6 | a0001c0002t0017g0006 a0001c0002t0017g0007 a0001c0002t0029g0017 others(3): Show |
6 | HG01243.hp2 HG02895.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2901-1254_2901-125 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(1): Show |
51 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(48): Show |
51 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2901-1257_2901-125 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(2): Show |
22 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0127 others(19): Show |
22 | HG00423.hp2 HG00639.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2901-1258_2901-125 others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005g0263 a0001c0001t0005g0304 a0001c0001t0006g0123 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901-1259_2901-125 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0336 a0001c0002t0033g0012 |
2 | HG00408.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2901-1260_2901-125 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(5): Show |
22 | a0001c0001t0001g0016 a0001c0001t0001g0274 a0001c0001t0001g0277 others(19): Show |
22 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2901-1261_2901-125 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(6): Show |
35 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0091 others(32): Show |
35 | HG00323.hp1 HG00423.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.2901-1262_2901-125 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(7): Show |
20 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0090 others(17): Show |
20 | HG00741.hp2 HG01070.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.2901-1263_2901-125 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0092 a0001c0001t0001g0276 a0001c0001t0001g0323 others(5): Show |
8 | HG01071.hp1 HG01109.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2901-1264_2901-125 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0009g0243 others(1): Show |
4 | HG01516.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2901-1265_2901-125 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(10): Show |
9 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0129 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2901-1266_2901-125 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(11): Show |
19 | a0001c0001t0002g0117 a0001c0001t0002g0128 a0001c0001t0002g0130 others(16): Show |
19 | HG00140.hp1 HG01070.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2901-1267_2901-125 others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(12): Show |
9 | a0002c0003t0002g0099 a0002c0003t0002g0215 a0002c0003t0002g0218 others(6): Show |
9 | HG00733.hp1 HG01515.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.2901-1268_2901-125 others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(13): Show |
19 | a0001c0001t0001g0264 a0001c0001t0002g0108 a0001c0001t0002g0114 others(16): Show |
19 | HG00558.hp2 HG00673.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2901-1269_2901-125 others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(14): Show |
16 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0115 others(13): Show |
16 | HG01433.hp1 HG01975.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0002g0124 a0001c0001t0005g0038 |
2 | NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(26): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0008g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(19): Show |
2 | a0001c0001t0052g0265 a0002c0003t0002g0238 |
2 | HG01167.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(20): Show |
3 | a0001c0001t0005g0252 a0001c0001t0013g0271 a0001c0001t0013g0272 |
3 | NA18906.hp1 NA19043.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(31): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(40): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0013g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(43): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(35): Show |
1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(46): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686408 | C | CAAAAAAA others(37): Show |
1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(48): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | |||||||
chr11:77686452 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2901-1293G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686452 | |||||||
chr11:77686678 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1519C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686678 | |||||||
chr11:77686679 | G | T | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1520C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686679 | |||||||
chr11:77686680 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1521A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686680 | |||||||
chr11:77686682 | T | G | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1523A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686682 | |||||||
chr11:77686683 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1524C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686683 | |||||||
chr11:77686687 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1528T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686687 | |||||||
chr11:77686688 | A | T | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1529T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686688 | |||||||
chr11:77686816 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2901-1657A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686816 | |||||||
chr11:77687022 | A | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-1863T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687022 | |||||||
chr11:77687169 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2901-2010C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687169 | |||||||
chr11:77687253 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2901-2094C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687253 | |||||||
chr11:77687408 | A | G | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2901-2249T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687408 | |||||||
chr11:77687523 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2901-2364A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687523 | |||||||
chr11:77687564 | G | C | 107 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(104): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2901-2405C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687564 | |||||||
chr11:77687576 | G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2901-2417C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687576 | |||||||
chr11:77687631 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2901-2472A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687631 | |||||||
chr11:77687742 | A | G | 6 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 others(3): Show |
6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2901-2583T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687742 | |||||||
chr11:77687838 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2901-2679T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687838 | |||||||
chr11:77687870 | C | T | 265 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(262): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2901-2711G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687870 | |||||||
chr11:77687871 | A | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2901-2712T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687871 | |||||||
chr11:77688292 | T | C | 271 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(268): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.2900+2867A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688292 | |||||||
chr11:77688368 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0289 |
2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2900+2791A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688368 | |||||||
chr11:77688429 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2900+2730A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688429 | |||||||
chr11:77688557 | G | T | 44 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2900+2602C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688557 | |||||||
chr11:77688838 | A | C | 12 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(9): Show |
12 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.2900+2321T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688838 | |||||||
chr11:77689018 | C | T | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0051g0182 |
3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2900+2141G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689018 | |||||||
chr11:77689240 | C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2900+1919G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689240 | |||||||
chr11:77689252 | A | T | 16 | a0001c0002t0003g0032 a0001c0002t0003g0033 a0001c0002t0003g0035 others(13): Show |
16 | HG01081.hp1 HG02257.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2900+1907T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689252 | |||||||
chr11:77689333 | T | C | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2900+1826A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689333 | |||||||
chr11:77689485 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2900+1674G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689485 | |||||||
chr11:77689584 | A | G | 3 | a0001c0001t0004g0149 a0001c0001t0004g0169 a0001c0001t0004g0175 |
3 | HG01167.hp1 HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2900+1575T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689584 | |||||||
chr11:77689680 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2900+1479T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689680 | |||||||
chr11:77689958 | T | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2900+1201A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689958 | |||||||
chr11:77690023 | G | A | 1 | a0001c0001t0044g0138 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2900+1136C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690023 | |||||||
chr11:77690161 | C | CA | 36 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0264 others(33): Show |
36 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2900+997dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690161 | |||||||
chr11:77690161 | CA | C | 81 | a0001c0001t0001g0335 a0001c0002t0003g0018 a0001c0002t0003g0019 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2900+997delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690161 | |||||||
chr11:77690172 | A | C | 2 | a0001c0002t0015g0074 a0001c0002t0024g0031 |
2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2900+987T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690172 | |||||||
chr11:77690173 | A | C | 80 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2900+986T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690173 | |||||||
chr11:77690175 | A | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2900+984T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690175 | |||||||
chr11:77690181 | C | A | 2 | a0001c0001t0005g0252 a0001c0001t0023g0251 |
2 | HG02630.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2900+978G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690181 | |||||||
chr11:77690182 | A | T | 76 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2900+977T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690182 | |||||||
chr11:77690353 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2900+806A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690353 | |||||||
chr11:77690586 | C | G | 1 | a0001c0001t0005g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2900+573G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690586 | |||||||
chr11:77690629 | A | C | 1 | a0001c0001t0001g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2900+530T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690629 | |||||||
chr11:77690815 | C | T | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2900+344G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690815 | |||||||
chr11:77691069 | C | A | 3 | a0001c0001t0001g0302 a0001c0001t0001g0305 a0007c0012t0001g0281 |
3 | HG00423.hp1 HG00558.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2900+90G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77691069 | |||||||
chr11:77691127 | C | T | 1 | a0001c0001t0067g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2900+32G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77691127 | |||||||
chr11:77691367 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2821-129C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691367 | |||||||
chr11:77691374 | T | C | 72 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.2821-136A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691374 | |||||||
chr11:77691448 | A | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2821-210T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691448 | |||||||
chr11:77691644 | T | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2821-406A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691644 | |||||||
chr11:77691689 | C | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2821-451G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691689 | |||||||
chr11:77691744 | A | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2821-506T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691744 | |||||||
chr11:77691820 | T | C | 1 | a0001c0001t0013g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2821-582A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691820 | |||||||
chr11:77692205 | T | A | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2821-967A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692205 | |||||||
chr11:77692221 | TACTACTT others(315): Show |
T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2820+964_2821-984d others(2): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692221 | |||||||
chr11:77692233 | A | AT | 17 | a0001c0001t0004g0134 a0001c0001t0004g0135 a0001c0001t0004g0139 others(14): Show |
17 | HG00609.hp1 HG01069.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2821-996dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATT | 11 | a0001c0001t0004g0143 a0001c0001t0004g0147 a0001c0001t0004g0148 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2821-997_2821-996d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTT | 21 | a0001c0001t0043g0153 a0002c0003t0002g0099 a0002c0003t0002g0208 others(18): Show |
21 | HG00558.hp2 HG01070.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.2821-998_2821-996d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTT | 14 | a0002c0003t0002g0203 a0002c0003t0002g0212 a0002c0003t0002g0214 others(11): Show |
14 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2821-999_2821-996d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTT | 7 | a0001c0001t0002g0114 a0001c0001t0002g0124 a0002c0003t0002g0207 others(4): Show |
7 | HG00140.hp1 HG01123.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2821-1000_2821-996 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTT | 7 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0115 others(4): Show |
7 | HG02602.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2821-1001_2821-996 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT | 12 | a0001c0001t0002g0108 a0001c0001t0002g0111 a0001c0001t0002g0126 others(9): Show |
12 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2821-1002_2821-996 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(1): Show |
6 | a0001c0001t0002g0112 a0001c0001t0002g0117 a0001c0001t0008g0267 others(3): Show |
6 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2821-1003_2821-996 others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0311 a0001c0001t0002g0003 a0001c0001t0002g0004 others(6): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.2821-1004_2821-996 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(3): Show |
32 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0274 others(29): Show |
32 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2821-1005_2821-996 others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(4): Show |
35 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(32): Show |
35 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.2821-1006_2821-996 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(5): Show |
9 | a0001c0001t0001g0277 a0001c0001t0001g0285 a0001c0001t0001g0288 others(6): Show |
9 | HG01109.hp2 HG01175.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2821-1007_2821-996 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(6): Show |
6 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0093 others(3): Show |
6 | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2821-1008_2821-996 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0001g0308 a0001c0001t0001g0321 a0001c0001t0001g0326 others(1): Show |
4 | HG02132.hp2 HG02886.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2821-1009_2821-996 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0279 a0001c0001t0001g0334 |
2 | NA18991.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2821-1010_2821-996 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0301 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2821-1012_2821-996 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2821-1013_2821-996 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2821-1017_2821-996 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | A | ATTTTTTT others(21): Show |
1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2821-1023_2821-996 others(31): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | AT | A | 7 | a0001c0001t0004g0107 a0001c0001t0004g0150 a0001c0001t0004g0198 others(4): Show |
7 | HG01975.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2821-996delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692233 | ATTTTTTT others(2): Show |
A | 15 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(12): Show |
15 | HG01975.hp2 HG02056.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.2821-1004_2821-996 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | |||||||
chr11:77692268 | G | A | 46 | a0001c0001t0004g0247 a0001c0001t0004g0248 a0002c0003t0002g0099 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2821-1030C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692268 | |||||||
chr11:77692345 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2821-1107G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692345 | |||||||
chr11:77692370 | A | G | 1 | a0001c0001t0040g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2821-1132T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692370 | |||||||
chr11:77692495 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2820+1012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692495 | |||||||
chr11:77692656 | C | G | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2820+851G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692656 | |||||||
chr11:77692681 | GT | G | 261 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(258): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.2820+825delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692681 | |||||||
chr11:77692685 | T | G | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2820+822A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692685 | |||||||
chr11:77692686 | T | G | 76 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(73): Show |
76 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2820+821A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692686 | |||||||
chr11:77692745 | T | C | 4 | a0001c0002t0010g0013 a0001c0002t0010g0350 a0001c0002t0010g0351 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2820+762A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692745 | |||||||
chr11:77692820 | G | C | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2820+687C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692820 | |||||||
chr11:77692878 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2820+629T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692878 | |||||||
chr11:77693065 | A | C | 1 | a0001c0002t0003g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2820+442T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693065 | |||||||
chr11:77693229 | C | G | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2820+278G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693229 | |||||||
chr11:77693352 | C | G | 4 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0005t0049g0202 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2820+155G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693352 | |||||||
chr11:77693764 | C | CATTT | 140 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(137): Show |
140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2716-157_2716-154d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693764 | C | CATTTATT others(1): Show |
23 | a0001c0001t0001g0016 a0001c0001t0001g0280 a0001c0001t0001g0305 others(20): Show |
23 | HG00099.hp2 HG00423.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2716-161_2716-154d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693764 | C | CATTTATT others(5): Show |
18 | a0001c0001t0001g0302 a0001c0001t0001g0316 a0002c0003t0002g0212 others(15): Show |
18 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.2716-165_2716-154d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693764 | C | CATTTATT others(9): Show |
20 | a0001c0001t0001g0317 a0002c0003t0002g0099 a0002c0003t0002g0205 others(17): Show |
20 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2716-169_2716-154d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693764 | CATTT | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0119 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2716-157_2716-154d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693764 | CATTTATT others(5): Show |
C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-165_2716-154d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | |||||||
chr11:77693871 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2716-260C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693871 | |||||||
chr11:77694096 | A | T | 109 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(106): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2716-485T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694096 | |||||||
chr11:77694147 | G | T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-536C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694147 | |||||||
chr11:77694221 | T | A | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2716-610A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694221 | |||||||
chr11:77694417 | C | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2716-806G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694417 | |||||||
chr11:77694522 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-911A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694522 | |||||||
chr11:77694769 | A | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-1158T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694769 | |||||||
chr11:77694798 | A | C | 2 | a0001c0002t0003g0061 a0001c0002t0003g0077 |
2 | NA18942.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2716-1187T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694798 | |||||||
chr11:77695212 | A | G | 2 | a0002c0003t0002g0208 a0002c0003t0002g0227 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2716-1601T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695212 | |||||||
chr11:77695237 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0292 a0001c0001t0001g0332 |
3 | NA19005.hp1 NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2716-1626T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695237 | |||||||
chr11:77695667 | C | T | 2 | a0001c0001t0004g0157 a0001c0001t0004g0167 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2716-2056G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695667 | |||||||
chr11:77695840 | A | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2716-2229T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695840 | |||||||
chr11:77695943 | C | T | 22 | a0001c0002t0003g0018 a0001c0002t0003g0053 a0001c0002t0003g0054 others(19): Show |
22 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2716-2332G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695943 | |||||||
chr11:77696030 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2716-2419C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696030 | |||||||
chr11:77696081 | A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2715+2406T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696081 | |||||||
chr11:77696489 | A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2715+1998T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696489 | |||||||
chr11:77696554 | CCCATTTT others(1): Show |
C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1925_2715+193 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696554 | |||||||
chr11:77696607 | A | T | 268 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(265): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2715+1880T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696607 | |||||||
chr11:77696711 | A | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2715+1776T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696711 | |||||||
chr11:77697234 | G | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1253C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697234 | |||||||
chr11:77697288 | C | T | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2715+1199G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697288 | |||||||
chr11:77697381 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1106A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697381 | |||||||
chr11:77697398 | A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2715+1089T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697398 | |||||||
chr11:77697441 | TATATATA others(39): Show |
T | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2715+1000_2715+104 others(50): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697441 | |||||||
chr11:77697600 | T | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2715+887A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697600 | |||||||
chr11:77697694 | A | T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+793T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697694 | |||||||
chr11:77697695 | T | A | 1 | a0001c0001t0004g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2715+792A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697695 | |||||||
chr11:77697832 | C | T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+655G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697832 | |||||||
chr11:77697849 | A | G | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2715+638T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697849 | |||||||
chr11:77697987 | T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2715+500A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697987 | |||||||
chr11:77698073 | T | G | 112 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(109): Show |
112 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2715+414A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698073 | |||||||
chr11:77698201 | G | A | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2715+286C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698201 | |||||||
chr11:77698289 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2715+198C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698289 | |||||||
chr11:77698297 | A | G | 2 | a0001c0001t0008g0267 a0002c0003t0008g0266 |
2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2715+190T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698297 | |||||||
chr11:77698362 | C | T | 67 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2715+125G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698362 | |||||||
chr11:77698787 | C | T | 74 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.2509-94G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698787 | |||||||
chr11:77698814 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2509-121A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698814 | |||||||
chr11:77698908 | C | T | 1 | a0012c0008t0003g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2509-215G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698908 | |||||||
chr11:77699003 | C | T | 2 | a0001c0002t0003g0050 a0001c0002t0003g0059 |
2 | HG00280.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2509-310G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699003 | |||||||
chr11:77699061 | T | C | 2 | a0002c0003t0002g0208 a0002c0003t0002g0227 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2509-368A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699061 | |||||||
chr11:77699062 | A | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-369T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699062 | |||||||
chr11:77699361 | A | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-668T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699361 | |||||||
chr11:77699421 | G | GAAACTTA others(3): Show |
349 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(346): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2509-729_2509-728i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699421 | |||||||
chr11:77699471 | A | T | 1 | a0002c0003t0002g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2509-778T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699471 | |||||||
chr11:77699633 | C | T | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2509-940G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699633 | |||||||
chr11:77699662 | G | A | 4 | a0001c0001t0004g0137 a0001c0001t0004g0150 a0001c0001t0004g0185 others(1): Show |
4 | HG00609.hp1 HG02523.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-969C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699662 | |||||||
chr11:77699823 | T | C | 1 | a0001c0002t0003g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2508+898A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699823 | |||||||
chr11:77699858 | A | G | 9 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(6): Show |
9 | HG02602.hp2 HG03654.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.2508+863T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699858 | |||||||
chr11:77700136 | A | G | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2508+585T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700136 | |||||||
chr11:77700300 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2508+421C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700300 | |||||||
chr11:77700328 | C | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2508+393G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700328 | |||||||
chr11:77700349 | C | CA | 17 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0103 others(14): Show |
17 | HG00597.hp2 HG00741.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2508+371dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | C | CAA | 20 | a0001c0001t0001g0286 a0001c0001t0001g0308 a0001c0001t0001g0342 others(17): Show |
20 | HG00609.hp1 HG01074.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.2508+370_2508+371d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | C | CAAA | 66 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0088 others(63): Show |
66 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2508+369_2508+371d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | C | CAAAA | 20 | a0001c0001t0001g0087 a0001c0001t0001g0097 a0001c0001t0001g0276 others(17): Show |
20 | HG01123.hp2 HG01261.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2508+368_2508+371d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | C | CCA | 3 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0052g0265 |
3 | HG02572.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2508+371_2508+372i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | CA | C | 118 | a0001c0001t0002g0109 a0001c0001t0002g0113 a0001c0001t0002g0114 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2508+371delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | CAA | C | 6 | a0001c0001t0006g0127 a0001c0002t0003g0022 a0001c0002t0017g0006 others(3): Show |
6 | HG01168.hp2 HG01243.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508+370_2508+371d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700349 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0013g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2508+361_2508+371d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | |||||||
chr11:77700361 | A | C | 1 | a0001c0001t0013g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2508+360T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700361 | |||||||
chr11:77702552 | T | C | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.734-57A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77702552 | |||||||
chr11:77702780 | A | G | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.734-285T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77702780 | |||||||
chr11:77703337 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-842A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703337 | |||||||
chr11:77703466 | A | T | 2 | a0001c0002t0014g0009 a0001c0002t0014g0011 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.734-971T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703466 | |||||||
chr11:77703809 | A | AAT | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1315_734-1314i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703809 | |||||||
chr11:77703887 | C | T | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1392G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703887 | |||||||
chr11:77704187 | G | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1692C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704187 | |||||||
chr11:77704497 | G | A | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-2002C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704497 | |||||||
chr11:77704520 | G | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(108): Show |
111 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.734-2025C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704520 | |||||||
chr11:77704529 | T | C | 81 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-2034A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704529 | |||||||
chr11:77704732 | G | T | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-2237C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704732 | |||||||
chr11:77704753 | G | GT | 35 | a0001c0001t0001g0016 a0001c0001t0001g0264 a0001c0001t0001g0274 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.734-2259dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | |||||||
chr11:77704753 | G | GTT | 10 | a0001c0001t0001g0287 a0001c0001t0001g0292 a0001c0001t0001g0332 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-2260_734-2259d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | |||||||
chr11:77704753 | G | GTTTTT | 57 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0021 others(54): Show |
57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.734-2263_734-2259d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | |||||||
chr11:77704753 | G | GTTTTTT | 6 | a0001c0002t0003g0020 a0001c0002t0003g0070 a0001c0002t0003g0083 others(3): Show |
6 | NA18950.hp1 NA18991.hp1 NA19078.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-2264_734-2259d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | |||||||
chr11:77704753 | GT | G | 70 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.734-2259delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | |||||||
chr11:77704775 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.734-2280C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704775 | |||||||
chr11:77704964 | G | A | 5 | a0001c0001t0004g0149 a0001c0001t0004g0169 a0001c0001t0004g0175 others(2): Show |
5 | HG01167.hp1 HG01261.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-2469C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704964 | |||||||
chr11:77705046 | T | C | 267 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.734-2551A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705046 | |||||||
chr11:77705234 | G | T | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.734-2739C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705234 | |||||||
chr11:77705247 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.734-2752C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705247 | |||||||
chr11:77705386 | G | T | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.734-2891C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705386 | |||||||
chr11:77705445 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0097 others(1): Show |
4 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2950G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705445 | |||||||
chr11:77705471 | T | C | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2976A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705471 | |||||||
chr11:77705825 | T | C | 2 | a0001c0001t0004g0157 a0001c0001t0004g0167 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.734-3330A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705825 | |||||||
chr11:77705861 | A | C | 191 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(188): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.734-3366T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705861 | |||||||
chr11:77705879 | C | A | 3 | a0002c0003t0002g0235 a0002c0003t0002g0236 a0002c0003t0002g0238 |
3 | HG00733.hp1 HG01167.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.734-3384G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705879 | |||||||
chr11:77705915 | A | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.734-3420T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705915 | |||||||
chr11:77706059 | C | T | 1 | a0001c0001t0019g0177 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.734-3564G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706059 | |||||||
chr11:77706089 | A | G | 9 | a0001c0001t0062g0283 a0001c0002t0014g0009 a0001c0002t0014g0011 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-3594T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706089 | |||||||
chr11:77706166 | G | A | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.734-3671C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706166 | |||||||
chr11:77706240 | C | CA | 23 | a0001c0001t0001g0095 a0001c0001t0001g0285 a0001c0001t0001g0327 others(20): Show |
23 | HG00741.hp2 HG01243.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.734-3746dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706240 | |||||||
chr11:77706314 | T | C | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.734-3819A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706314 | |||||||
chr11:77706347 | G | T | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.734-3852C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706347 | |||||||
chr11:77706663 | T | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-4168A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706663 | |||||||
chr11:77706699 | C | T | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.734-4204G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706699 | |||||||
chr11:77706864 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-4369A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706864 | |||||||
chr11:77707216 | G | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-4721C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707216 | |||||||
chr11:77707450 | T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.734-4955A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707450 | |||||||
chr11:77707657 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-5162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707657 | |||||||
chr11:77707835 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-5340G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707835 | |||||||
chr11:77707915 | C | T | 2 | a0001c0002t0017g0006 a0011c0018t0032g0014 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-5420G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707915 | |||||||
chr11:77708038 | C | T | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.734-5543G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708038 | |||||||
chr11:77708053 | T | A | 3 | a0002c0003t0002g0222 a0002c0003t0002g0223 a0002c0003t0002g0232 |
3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.734-5558A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708053 | |||||||
chr11:77708190 | T | C | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.734-5695A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708190 | |||||||
chr11:77708330 | G | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-5835C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708330 | |||||||
chr11:77708399 | C | T | 1 | a0001c0002t0030g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.734-5904G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708399 | |||||||
chr11:77708511 | A | T | 4 | a0002c0003t0002g0345 a0002c0003t0002g0346 a0002c0003t0002g0347 others(1): Show |
4 | HG01891.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-6016T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708511 | |||||||
chr11:77708754 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.734-6259G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708754 | |||||||
chr11:77708758 | C | G | 1 | a0001c0001t0057g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.734-6263G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708758 | |||||||
chr11:77708774 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-6279A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708774 | |||||||
chr11:77708859 | C | T | 2 | a0002c0003t0002g0240 a0002c0003t0002g0241 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.734-6364G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708859 | |||||||
chr11:77708919 | G | A | 1 | a0003c0016t0045g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.734-6424C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708919 | |||||||
chr11:77708943 | T | C | 4 | a0001c0001t0002g0284 a0001c0001t0023g0275 a0004c0006t0012g0001 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-6448A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708943 | |||||||
chr11:77708971 | C | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.734-6476G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708971 | |||||||
chr11:77709143 | T | G | 1 | a0001c0001t0007g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.734-6648A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709143 | |||||||
chr11:77709269 | C | T | 272 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(269): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.734-6774G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709269 | |||||||
chr11:77709473 | A | T | 2 | a0001c0001t0038g0170 a0001c0001t0039g0166 |
2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.734-6978T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709473 | |||||||
chr11:77709537 | C | T | 6 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0123 others(3): Show |
6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-7042G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709537 | |||||||
chr11:77709546 | A | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.734-7051T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709546 | |||||||
chr11:77709694 | CT | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-7200delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709694 | |||||||
chr11:77709867 | G | C | 3 | a0001c0002t0010g0013 a0001c0002t0033g0012 a0011c0018t0032g0014 |
3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-7372C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709867 | |||||||
chr11:77710159 | TA | T | 6 | a0001c0001t0009g0243 a0001c0001t0009g0244 a0001c0002t0014g0009 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-7665delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710159 | |||||||
chr11:77710160 | A | T | 1 | a0001c0001t0055g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.734-7665T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710160 | |||||||
chr11:77710196 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-7701C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710196 | |||||||
chr11:77710231 | T | C | 8 | a0001c0001t0001g0274 a0001c0001t0001g0334 a0001c0001t0001g0336 others(5): Show |
8 | HG00408.hp1 HG00609.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-7736A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710231 | |||||||
chr11:77710359 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-7864A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710359 | |||||||
chr11:77710401 | T | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.734-7906A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710401 | |||||||
chr11:77710402 | T | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.734-7907A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710402 | |||||||
chr11:77710435 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.734-7940G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710435 | |||||||
chr11:77710502 | G | A | 1 | a0003c0005t0020g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.734-8007C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710502 | |||||||
chr11:77710506 | T | C | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.734-8011A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710506 | |||||||
chr11:77710536 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.734-8041G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710536 | |||||||
chr11:77711063 | A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.734-8568T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711063 | |||||||
chr11:77711108 | T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-8613A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711108 | |||||||
chr11:77711119 | C | A | 1 | a0001c0001t0004g0190 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-8624G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711119 | |||||||
chr11:77711120 | CT | C | 5 | a0001c0001t0001g0274 a0001c0001t0001g0334 a0001c0001t0001g0336 others(2): Show |
5 | HG00408.hp1 HG00609.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-8626delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711120 | |||||||
chr11:77711143 | T | TA | 16 | a0001c0001t0001g0276 a0001c0001t0001g0285 a0001c0001t0001g0298 others(13): Show |
16 | HG01256.hp2 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-8649dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | |||||||
chr11:77711143 | T | TAA | 62 | a0001c0001t0002g0003 a0001c0002t0003g0018 a0001c0002t0003g0020 others(59): Show |
62 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.734-8650_734-8649d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | |||||||
chr11:77711143 | T | TAAA | 7 | a0001c0002t0003g0019 a0001c0002t0014g0009 a0001c0002t0014g0011 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8651_734-8649d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | |||||||
chr11:77711143 | TA | T | 58 | a0001c0001t0001g0090 a0001c0001t0001g0307 a0001c0001t0002g0113 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-8649delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | |||||||
chr11:77711180 | T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.734-8685A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711180 | |||||||
chr11:77711287 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.734-8792T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711287 | |||||||
chr11:77711290 | C | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.734-8795G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711290 | |||||||
chr11:77711483 | AT | A | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8989delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711483 | |||||||
chr11:77711485 | G | A | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8990C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711485 | |||||||
chr11:77711540 | G | T | 1 | a0002c0004t0002g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.734-9045C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711540 | |||||||
chr11:77711590 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-9095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711590 | |||||||
chr11:77711671 | A | AAAAC | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-9180_734-9177d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711671 | |||||||
chr11:77711759 | C | T | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.734-9264G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711759 | |||||||
chr11:77711790 | T | G | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.734-9295A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711790 | |||||||
chr11:77711939 | C | T | 4 | a0001c0001t0002g0284 a0001c0001t0023g0275 a0004c0006t0012g0001 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-9444G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711939 | |||||||
chr11:77712002 | AGATT | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-9511_734-9508d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712002 | |||||||
chr11:77712142 | T | C | 1 | a0001c0001t0004g0190 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-9647A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712142 | |||||||
chr11:77712675 | T | C | 1 | a0001c0001t0007g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.734-10180A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712675 | |||||||
chr11:77712806 | T | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.734-10311A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712806 | |||||||
chr11:77712906 | C | T | 1 | a0001c0002t0003g0020 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.734-10411G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712906 | |||||||
chr11:77712981 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-10486A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712981 | |||||||
chr11:77713201 | T | G | 2 | a0001c0001t0038g0170 a0001c0001t0039g0166 |
2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.734-10706A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713201 | |||||||
chr11:77713223 | G | A | 9 | a0001c0001t0004g0100 a0001c0001t0004g0193 a0001c0001t0004g0194 others(6): Show |
9 | HG01975.hp1 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-10728C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713223 | |||||||
chr11:77713315 | G | C | 1 | a0001c0001t0005g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.734-10820C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713315 | |||||||
chr11:77713476 | T | C | 1 | a0001c0001t0004g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.734-10981A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713476 | |||||||
chr11:77713573 | A | G | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.734-11078T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713573 | |||||||
chr11:77713576 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-11081C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713576 | |||||||
chr11:77714040 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0176 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+11505G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714040 | |||||||
chr11:77714114 | A | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0176 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+11431T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714114 | |||||||
chr11:77714272 | T | C | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.733+11273A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714272 | |||||||
chr11:77714552 | G | C | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+10993C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714552 | |||||||
chr11:77714660 | G | C | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.733+10885C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714660 | |||||||
chr11:77714710 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+10835G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714710 | |||||||
chr11:77714711 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+10834C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714711 | |||||||
chr11:77714745 | G | C | 22 | a0001c0001t0001g0264 a0001c0001t0005g0038 a0001c0001t0005g0252 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.733+10800C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714745 | |||||||
chr11:77714842 | T | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+10703A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714842 | |||||||
chr11:77714943 | A | C | 68 | a0001c0001t0004g0176 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.733+10602T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714943 | |||||||
chr11:77715050 | G | A | 108 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(105): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.733+10495C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715050 | |||||||
chr11:77715109 | G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+10436C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715109 | |||||||
chr11:77715148 | G | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+10397C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715148 | |||||||
chr11:77715206 | T | C | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0117 |
3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.733+10339A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715206 | |||||||
chr11:77715227 | T | C | 9 | a0001c0001t0001g0274 a0001c0001t0001g0334 a0001c0001t0001g0336 others(6): Show |
9 | HG00408.hp1 HG00609.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.733+10318A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715227 | |||||||
chr11:77715230 | C | CA | 72 | a0001c0001t0004g0176 a0001c0002t0003g0018 a0001c0002t0003g0019 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.733+10314dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715230 | |||||||
chr11:77715300 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.733+10245A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715300 | |||||||
chr11:77715379 | ATGT | A | 4 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(1): Show |
4 | HG02622.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+10163_733+1016 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715379 | |||||||
chr11:77715400 | T | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+10145A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715400 | |||||||
chr11:77715457 | TA | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+10087delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715457 | |||||||
chr11:77715499 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+10046C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715499 | |||||||
chr11:77715508 | C | T | 2 | a0002c0003t0002g0345 a0002c0003t0002g0347 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.733+10037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715508 | |||||||
chr11:77715551 | G | A | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+9994C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715551 | |||||||
chr11:77715670 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+9875T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715670 | |||||||
chr11:77715694 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+9851G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715694 | |||||||
chr11:77715779 | T | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0176 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+9766A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715779 | |||||||
chr11:77716531 | T | G | 1 | a0002c0004t0002g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.733+9014A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716531 | |||||||
chr11:77716701 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+8844G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716701 | |||||||
chr11:77716722 | T | C | 1 | a0001c0002t0003g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733+8823A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716722 | |||||||
chr11:77716732 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+8813A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716732 | |||||||
chr11:77716933 | T | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+8612A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716933 | |||||||
chr11:77717119 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+8426T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717119 | |||||||
chr11:77717156 | CA | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0176 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.733+8388delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717156 | |||||||
chr11:77717166 | A | C | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.733+8379T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717166 | |||||||
chr11:77717181 | CA | C | 259 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(256): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.733+8363delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717181 | |||||||
chr11:77717627 | T | C | 1 | a0002c0003t0002g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733+7918A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717627 | |||||||
chr11:77717794 | A | T | 1 | a0002c0003t0002g0219 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.733+7751T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717794 | |||||||
chr11:77717888 | C | T | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.733+7657G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717888 | |||||||
chr11:77718260 | C | T | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.733+7285G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718260 | |||||||
chr11:77718263 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0126 |
2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.733+7282C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718263 | |||||||
chr11:77718302 | G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+7243C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718302 | |||||||
chr11:77718350 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.733+7195A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718350 | |||||||
chr11:77718534 | T | C | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.733+7011A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718534 | |||||||
chr11:77718879 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+6666A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718879 | |||||||
chr11:77718908 | A | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+6637T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718908 | |||||||
chr11:77718987 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+6558C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718987 | |||||||
chr11:77719015 | G | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+6530C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719015 | |||||||
chr11:77719134 | C | T | 3 | a0001c0001t0022g0140 a0001c0001t0022g0141 a0001c0001t0054g0142 |
3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.733+6411G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719134 | |||||||
chr11:77719147 | T | C | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.733+6398A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719147 | |||||||
chr11:77719405 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+6140T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719405 | |||||||
chr11:77719555 | A | C | 2 | a0001c0002t0010g0013 a0001c0002t0033g0012 |
2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.733+5990T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719555 | |||||||
chr11:77719607 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+5938G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719607 | |||||||
chr11:77719608 | A | T | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.733+5937T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719608 | |||||||
chr11:77720013 | G | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+5532C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720013 | |||||||
chr11:77720123 | A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+5422T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720123 | |||||||
chr11:77720146 | C | T | 1 | a0002c0003t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.733+5399G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720146 | |||||||
chr11:77720175 | G | T | 6 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0123 others(3): Show |
6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+5370C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720175 | |||||||
chr11:77720184 | G | A | 75 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.733+5361C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720184 | |||||||
chr11:77720261 | C | T | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+5284G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720261 | |||||||
chr11:77720289 | G | A | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(155): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.733+5256C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720289 | |||||||
chr11:77720590 | G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+4955C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720590 | |||||||
chr11:77720822 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+4723A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720822 | |||||||
chr11:77721039 | T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+4506A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721039 | |||||||
chr11:77721459 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4086C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721459 | |||||||
chr11:77721816 | C | CTGAA | 6 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0016g0005 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+3725_733+3728d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721816 | |||||||
chr11:77721932 | G | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.733+3613C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721932 | |||||||
chr11:77722019 | A | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+3526T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722019 | |||||||
chr11:77722444 | T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.733+3101A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722444 | |||||||
chr11:77722482 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+3063A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722482 | |||||||
chr11:77722899 | C | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2646G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722899 | |||||||
chr11:77723080 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2465G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723080 | |||||||
chr11:77723216 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2329A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723216 | |||||||
chr11:77723239 | G | A | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0051g0182 |
3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.733+2306C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723239 | |||||||
chr11:77723341 | G | A | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+2204C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723341 | |||||||
chr11:77723368 | GGCTGGGA others(33): Show |
G | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.733+2137_733+2176d others(42): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723368 | |||||||
chr11:77723393 | T | C | 1 | a0001c0001t0063g0291 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.733+2152A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723393 | |||||||
chr11:77723420 | A | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2125T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723420 | |||||||
chr11:77723441 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+2104G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723441 | |||||||
chr11:77723497 | G | A | 264 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(261): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.733+2048C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723497 | |||||||
chr11:77723717 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.733+1828A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723717 | |||||||
chr11:77723886 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+1659A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723886 | |||||||
chr11:77724110 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.733+1435A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724110 | |||||||
chr11:77724633 | T | C | 2 | a0002c0003t0002g0208 a0002c0003t0002g0227 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.733+912A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724633 | |||||||
chr11:77724659 | T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+886A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724659 | |||||||
chr11:77724786 | G | A | 108 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(105): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.733+759C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724786 | |||||||
chr11:77724890 | G | C | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+655C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724890 | |||||||
chr11:77724931 | C | A | 3 | a0002c0003t0002g0216 a0002c0003t0002g0221 a0002c0003t0002g0229 |
3 | HG01070.hp2 HG01168.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.733+614G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724931 | |||||||
chr11:77725154 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.733+391A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725154 | |||||||
chr11:77725435 | C | T | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.733+110G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725435 | |||||||
chr11:77725472 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+73A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725472 | |||||||
chr11:77725966 | T | G | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-267A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77725966 | |||||||
chr11:77726943 | A | C | 1 | a0001c0001t0051g0182 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.579-1244T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77726943 | |||||||
chr11:77726953 | A | C | 2 | a0001c0002t0014g0009 a0001c0002t0014g0011 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.579-1254T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77726953 | |||||||
chr11:77727014 | A | G | 71 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.579-1315T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727014 | |||||||
chr11:77727042 | C | A | 2 | a0001c0001t0005g0263 a0001c0001t0060g0257 |
2 | NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.579-1343G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727042 | |||||||
chr11:77727329 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.579-1630G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727329 | |||||||
chr11:77727473 | C | CT | 174 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.579-1775dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | |||||||
chr11:77727473 | C | CTT | 16 | a0001c0001t0009g0243 a0001c0001t0009g0244 a0001c0002t0003g0019 others(13): Show |
16 | HG01074.hp1 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.579-1776_579-1775d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | |||||||
chr11:77727473 | C | CTTT | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.579-1777_579-1775d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | |||||||
chr11:77727692 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.579-1993G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727692 | |||||||
chr11:77727759 | C | T | 1 | a0001c0001t0007g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.579-2060G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727759 | |||||||
chr11:77727867 | T | C | 6 | a0002c0003t0002g0207 a0002c0003t0002g0225 a0002c0003t0002g0345 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-2168A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727867 | |||||||
chr11:77727947 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-2248T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727947 | |||||||
chr11:77728049 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-2350A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728049 | |||||||
chr11:77728450 | A | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-2751T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728450 | |||||||
chr11:77728464 | C | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-2765G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728464 | |||||||
chr11:77728465 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0048g0156 |
3 | HG02895.hp2 HG02897.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.579-2766C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728465 | |||||||
chr11:77728500 | C | CAGGAA | 6 | a0001c0001t0002g0108 a0001c0001t0009g0242 a0001c0001t0009g0243 others(3): Show |
6 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-2806_579-2802d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728500 | |||||||
chr11:77728500 | CAGGAA | C | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0117 |
3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579-2806_579-2802d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728500 | |||||||
chr11:77728866 | T | TAA | 77 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(74): Show |
77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.579-3169_579-3168d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728866 | |||||||
chr11:77729027 | G | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-3328C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729027 | |||||||
chr11:77729061 | A | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-3362T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729061 | |||||||
chr11:77729163 | T | A | 80 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(77): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.579-3464A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729163 | |||||||
chr11:77729163 | T | G | 33 | a0001c0001t0001g0264 a0001c0001t0001g0276 a0001c0001t0001g0277 others(30): Show |
33 | HG01074.hp2 HG01433.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.579-3464A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729163 | |||||||
chr11:77729574 | C | A | 1 | a0001c0001t0066g0173 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.579-3875G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729574 | |||||||
chr11:77729607 | T | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579-3908A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729607 | |||||||
chr11:77729641 | C | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.579-3942G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729641 | |||||||
chr11:77729776 | T | G | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.579-4077A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729776 | |||||||
chr11:77729895 | C | CA | 14 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0001t0004g0135 others(11): Show |
14 | HG00609.hp1 HG01175.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.579-4197dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(2): Show |
29 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0088 others(26): Show |
29 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-4205_579-4197d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(3): Show |
46 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(43): Show |
46 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.579-4206_579-4197d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(4): Show |
30 | a0001c0001t0001g0274 a0001c0001t0001g0287 a0001c0001t0001g0292 others(27): Show |
30 | HG00423.hp1 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579-4207_579-4197d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0332 a0001c0001t0001g0344 a0001c0001t0002g0112 others(12): Show |
15 | HG00673.hp2 HG02027.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.579-4208_579-4197d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0115 a0001c0001t0002g0119 a0001c0001t0009g0242 others(4): Show |
7 | HG01516.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-4209_579-4197d others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0286 a0001c0001t0001g0289 a0001c0002t0010g0350 others(1): Show |
4 | HG02055.hp2 NA18981.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-4210_579-4197d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0279 a0001c0001t0001g0333 a0001c0001t0002g0114 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-4211_579-4197d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.579-4212_579-4197d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0006g0123 a0001c0001t0006g0125 a0001c0001t0006g0127 |
3 | HG02486.hp2 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.579-4213_579-4197d others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.579-4214_579-4197d others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(13): Show |
1 | a0002c0003t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.579-4216_579-4197d others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(14): Show |
8 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(5): Show |
8 | HG00639.hp1 HG01975.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.579-4217_579-4197d others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0005g0261 a0001c0001t0041g0249 a0002c0003t0008g0266 others(1): Show |
4 | HG02717.hp2 HG04228.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-4218_579-4197d others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0005g0254 a0001c0001t0008g0267 a0001c0001t0025g0259 |
3 | HG03710.hp1 NA18977.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.579-4219_579-4197d others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.579-4220_579-4197d others(26): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(19): Show |
3 | a0001c0001t0005g0263 a0001c0001t0008g0268 a0001c0001t0009g0245 |
3 | HG01074.hp2 HG03209.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.579-4222_579-4197d others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0008g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.579-4224_579-4197d others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0008g0270 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.579-4197_579-4196i others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | CA | C | 13 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0004g0143 others(10): Show |
13 | HG00140.hp1 HG00733.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.579-4197delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | CAAAAAA | C | 51 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(48): Show |
51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.579-4202_579-4197d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | CAAAAAAA | C | 25 | a0001c0002t0003g0032 a0001c0002t0003g0035 a0001c0002t0003g0036 others(22): Show |
25 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.579-4203_579-4197d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77729895 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0002g0284 a0001c0001t0023g0275 a0001c0001t0040g0116 others(2): Show |
5 | HG02451.hp1 HG02602.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-4208_579-4197d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | |||||||
chr11:77730039 | A | C | 1 | a0002c0003t0002g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.579-4340T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730039 | |||||||
chr11:77730257 | T | C | 1 | a0001c0001t0008g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579-4558A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730257 | |||||||
chr11:77730276 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.579-4577A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730276 | |||||||
chr11:77730285 | T | G | 1 | a0001c0001t0007g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.579-4586A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730285 | |||||||
chr11:77730295 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.579-4596A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730295 | |||||||
chr11:77730337 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-4638G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730337 | |||||||
chr11:77730546 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-4847G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730546 | |||||||
chr11:77730673 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579-4974T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730673 | |||||||
chr11:77730676 | G | A | 79 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.579-4977C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730676 | |||||||
chr11:77730758 | G | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-5059C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730758 | |||||||
chr11:77730803 | G | A | 1 | a0002c0003t0021g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.579-5104C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730803 | |||||||
chr11:77730853 | C | T | 1 | a0001c0001t0027g0260 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.579-5154G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730853 | |||||||
chr11:77730928 | A | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-5229T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730928 | |||||||
chr11:77730939 | G | A | 1 | a0001c0002t0003g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.579-5240C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730939 | |||||||
chr11:77731908 | G | A | 7 | a0001c0002t0003g0048 a0001c0002t0003g0052 a0001c0002t0003g0055 others(4): Show |
7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-6209C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77731908 | |||||||
chr11:77731979 | G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579-6280C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77731979 | |||||||
chr11:77732048 | G | A | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.579-6349C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732048 | |||||||
chr11:77732103 | G | T | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.579-6404C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732103 | |||||||
chr11:77732161 | C | G | 2 | a0001c0001t0004g0149 a0001c0001t0004g0175 |
2 | HG01167.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.579-6462G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732161 | |||||||
chr11:77732224 | T | C | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579-6525A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732224 | |||||||
chr11:77732339 | AGTCTCAC others(36): Show |
A | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-6683_579-6641d others(45): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732339 | |||||||
chr11:77732383 | T | A | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-6684A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732383 | |||||||
chr11:77732582 | G | A | 4 | a0001c0001t0013g0271 a0001c0001t0013g0272 a0001c0001t0013g0273 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-6883C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732582 | |||||||
chr11:77732641 | G | A | 8 | a0001c0001t0001g0285 a0001c0001t0001g0298 a0001c0001t0001g0299 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.579-6942C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732641 | |||||||
chr11:77732661 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.579-6962T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732661 | |||||||
chr11:77732671 | C | T | 3 | a0001c0001t0005g0253 a0001c0001t0005g0263 a0001c0001t0060g0257 |
3 | HG01975.hp2 NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.579-6972G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732671 | |||||||
chr11:77732859 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-7160A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732859 | |||||||
chr11:77733003 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.579-7304A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733003 | |||||||
chr11:77733346 | CTA | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7383_578+7384d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733346 | |||||||
chr11:77733424 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7307G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733424 | |||||||
chr11:77733434 | T | TTC | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7295_578+7296d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733434 | |||||||
chr11:77733447 | C | T | 2 | a0001c0001t0004g0136 a0001c0001t0042g0174 |
2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.578+7284G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733447 | |||||||
chr11:77733557 | AT | A | 93 | a0001c0001t0001g0095 a0001c0001t0001g0317 a0001c0001t0001g0334 others(90): Show |
93 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.578+7173delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733557 | |||||||
chr11:77733557 | ATT | A | 109 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(106): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.578+7172_578+7173d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733557 | |||||||
chr11:77733852 | A | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+6879T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733852 | |||||||
chr11:77733865 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.578+6866G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733865 | |||||||
chr11:77734236 | A | ATTCT | 79 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+6494_578+6495i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734236 | |||||||
chr11:77734239 | A | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+6492T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734239 | |||||||
chr11:77734246 | A | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+6485T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734246 | |||||||
chr11:77734301 | CT | C | 87 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0253 others(84): Show |
87 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.578+6429delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734301 | |||||||
chr11:77734308 | TG | T | 93 | a0001c0001t0001g0016 a0001c0001t0001g0264 a0001c0001t0001g0274 others(90): Show |
93 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.578+6422delC | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734308 | |||||||
chr11:77734309 | G | T | 1 | a0002c0003t0002g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.578+6422C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734309 | |||||||
chr11:77734310 | G | A | 51 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(48): Show |
51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.578+6421C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734310 | |||||||
chr11:77734354 | A | G | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.578+6377T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734354 | |||||||
chr11:77734386 | A | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.578+6345T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734386 | |||||||
chr11:77734556 | G | C | 2 | a0001c0001t0009g0243 a0001c0001t0009g0244 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.578+6175C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734556 | |||||||
chr11:77734679 | C | T | 1 | a0001c0001t0005g0293 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.578+6052G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734679 | |||||||
chr11:77734797 | C | T | 2 | a0001c0002t0003g0083 a0001c0002t0003g0084 |
2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.578+5934G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734797 | |||||||
chr11:77735006 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+5725A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735006 | |||||||
chr11:77735049 | C | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.578+5682G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735049 | |||||||
chr11:77735072 | C | T | 79 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+5659G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735072 | |||||||
chr11:77735096 | G | T | 1 | a0001c0002t0003g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.578+5635C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735096 | |||||||
chr11:77735179 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.578+5552G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735179 | |||||||
chr11:77735315 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0018 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+5416G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735315 | |||||||
chr11:77735536 | C | T | 1 | a0001c0002t0018g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.578+5195G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735536 | |||||||
chr11:77735810 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.578+4921C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735810 | |||||||
chr11:77735943 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+4788A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735943 | |||||||
chr11:77736003 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+4728G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736003 | |||||||
chr11:77736009 | T | G | 71 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.578+4722A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736009 | |||||||
chr11:77736023 | C | T | 79 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+4708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736023 | |||||||
chr11:77736434 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.578+4297G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736434 | |||||||
chr11:77736617 | T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.578+4114A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736617 | |||||||
chr11:77736693 | T | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+4038A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736693 | |||||||
chr11:77737166 | C | G | 269 | a0001c0001t0001g0264 a0001c0001t0001g0277 a0001c0001t0001g0290 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.578+3565G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737166 | |||||||
chr11:77737323 | C | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+3408G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737323 | |||||||
chr11:77737454 | C | CA | 13 | a0001c0001t0001g0286 a0001c0001t0001g0289 a0001c0001t0001g0307 others(10): Show |
13 | HG01433.hp2 HG02055.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.578+3276dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737454 | |||||||
chr11:77737467 | C | A | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.578+3264G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737467 | |||||||
chr11:77737469 | A | C | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.578+3262T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737469 | |||||||
chr11:77737472 | A | AAAC | 71 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(68): Show |
71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.578+3256_578+3258d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | |||||||
chr11:77737472 | A | AAACAAC | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+3253_578+3258d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | |||||||
chr11:77737472 | AAACAAC | A | 7 | a0001c0001t0001g0285 a0001c0001t0001g0298 a0001c0001t0001g0299 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+3253_578+3258d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | |||||||
chr11:77737487 | CAACAAA | C | 7 | a0001c0002t0003g0048 a0001c0002t0003g0052 a0001c0002t0003g0055 others(4): Show |
7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+3238_578+3243d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737487 | |||||||
chr11:77737490 | C | A | 2 | a0001c0001t0004g0157 a0001c0001t0004g0167 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.578+3241G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737490 | |||||||
chr11:77737493 | A | C | 75 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(72): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.578+3238T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737493 | |||||||
chr11:77737571 | T | C | 78 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.578+3160A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737571 | |||||||
chr11:77737606 | T | G | 1 | a0008c0011t0007g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.578+3125A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737606 | |||||||
chr11:77737607 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+3124A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737607 | |||||||
chr11:77737616 | TGG | T | 26 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0324 others(23): Show |
26 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.578+3113_578+3114d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737616 | |||||||
chr11:77737619 | G | GGT | 14 | a0001c0001t0001g0280 a0001c0001t0001g0305 a0001c0001t0001g0309 others(11): Show |
14 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGGGTG others(3): Show |
2 | a0001c0001t0004g0133 a0001c0001t0004g0165 |
2 | NA19007.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGGGTG others(9): Show |
1 | a0001c0001t0046g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.578+3111_578+3112i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGGGTG others(11): Show |
5 | a0001c0001t0004g0150 a0001c0001t0004g0185 a0001c0001t0011g0160 others(2): Show |
5 | HG00609.hp1 HG01192.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGGGTG others(15): Show |
2 | a0001c0001t0004g0137 a0001c0001t0004g0190 |
2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGGTGT others(4): Show |
1 | a0001c0001t0011g0172 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.578+3111_578+3112i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGT | 17 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0299 others(14): Show |
17 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGT | 16 | a0001c0001t0001g0286 a0001c0001t0001g0300 a0001c0001t0001g0334 others(13): Show |
16 | HG00323.hp2 HG01074.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(1): Show |
17 | a0001c0001t0001g0279 a0001c0001t0001g0295 a0001c0001t0001g0301 others(14): Show |
17 | HG00609.hp2 HG01346.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(3): Show |
8 | a0001c0001t0001g0298 a0001c0001t0001g0342 a0001c0001t0004g0103 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(5): Show |
26 | a0001c0001t0001g0016 a0001c0001t0001g0288 a0001c0001t0004g0136 others(23): Show |
26 | HG00099.hp1 HG00280.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0264 a0001c0001t0001g0297 a0001c0001t0004g0102 others(13): Show |
16 | HG01517.hp1 HG02015.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(9): Show |
9 | a0001c0001t0001g0289 a0001c0001t0001g0296 a0001c0001t0004g0101 others(6): Show |
9 | HG02572.hp1 HG03225.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(11): Show |
2 | a0001c0001t0001g0302 a0001c0001t0047g0104 |
2 | NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GGTGTGTG others(13): Show |
4 | a0001c0001t0004g0180 a0001c0001t0004g0250 a0001c0001t0042g0174 others(1): Show |
4 | HG03041.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0004g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.578+3111_578+3112i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGT | G | 65 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(62): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.578+3108_578+3111d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGTGT | G | 6 | a0001c0001t0001g0329 a0001c0002t0003g0040 a0001c0002t0003g0081 others(3): Show |
6 | HG02132.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+3106_578+3111d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.578+3102_578+3111d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGTGTG others(5): Show |
G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+3100_578+3111d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGTGTG others(19): Show |
G | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.578+3086_578+3111d others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737619 | GGGGTGTG others(21): Show |
G | 68 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.578+3084_578+3111d others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | |||||||
chr11:77737621 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0004g0196 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.578+3098_578+3109d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | |||||||
chr11:77737621 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.578+3096_578+3109d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | |||||||
chr11:77737621 | G | T | 164 | a0001c0001t0001g0016 a0001c0001t0001g0264 a0001c0001t0001g0279 others(161): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.578+3110C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | |||||||
chr11:77737667 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0066g0173 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.578+3063_578+3064i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737667 | |||||||
chr11:77737667 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0004g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.578+3063_578+3064i others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737667 | |||||||
chr11:77737686 | C | G | 3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0341 |
3 | HG02074.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.578+3045G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737686 | |||||||
chr11:77737728 | TGAAAGCA | T | 238 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.578+2996_578+3002d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737728 | |||||||
chr11:77737948 | A | T | 238 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.578+2783T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737948 | |||||||
chr11:77738157 | T | TAATTAAA others(1): Show |
3 | a0001c0002t0010g0013 a0001c0002t0033g0012 a0011c0018t0032g0014 |
3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.578+2573_578+2574i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738157 | |||||||
chr11:77738157 | T | TAGTTAAA others(1): Show |
79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+2566_578+2573d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738157 | |||||||
chr11:77738210 | G | A | 1 | a0001c0001t0065g0146 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.578+2521C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738210 | |||||||
chr11:77738280 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+2451C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738280 | |||||||
chr11:77738314 | A | AG | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+2416_578+2417i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738314 | |||||||
chr11:77738318 | GC | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+2412delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738318 | |||||||
chr11:77738359 | A | G | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.578+2372T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738359 | |||||||
chr11:77738492 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+2239C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738492 | |||||||
chr11:77738492 | G | C | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.578+2239C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738492 | |||||||
chr11:77738573 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+2158A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738573 | |||||||
chr11:77738733 | A | T | 261 | a0001c0001t0001g0264 a0001c0001t0002g0003 a0001c0001t0002g0004 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.578+1998T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738733 | |||||||
chr11:77738915 | C | T | 1 | a0002c0003t0021g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.578+1816G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738915 | |||||||
chr11:77739084 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578+1647G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739084 | |||||||
chr11:77739092 | A | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+1639T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739092 | |||||||
chr11:77739190 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578+1541G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739190 | |||||||
chr11:77739330 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+1401A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739330 | |||||||
chr11:77739403 | T | TA | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+1327_578+1328i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739403 | |||||||
chr11:77739467 | G | A | 1 | a0001c0001t0004g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.578+1264C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739467 | |||||||
chr11:77739542 | T | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.578+1189A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739542 | |||||||
chr11:77739827 | C | T | 1 | a0001c0002t0003g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.578+904G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739827 | |||||||
chr11:77739849 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+882C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739849 | |||||||
chr11:77739866 | T | C | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.578+865A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739866 | |||||||
chr11:77739913 | T | TA | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+817dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739913 | |||||||
chr11:77740115 | C | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.578+616G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740115 | |||||||
chr11:77740158 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.578+573G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740158 | |||||||
chr11:77740288 | T | C | 6 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0123 others(3): Show |
6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.578+443A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740288 | |||||||
chr11:77740336 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+395A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740336 | |||||||
chr11:77740370 | C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.578+361G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740370 | |||||||
chr11:77740476 | C | T | 1 | a0001c0001t0009g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.578+255G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740476 | |||||||
chr11:77740688 | C | T | 1 | a0001c0001t0007g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.578+43G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740688 | |||||||
chr11:77741015 | T | C | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.373-79A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741015 | |||||||
chr11:77741134 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.373-198T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741134 | |||||||
chr11:77741323 | G | A | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.373-387C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741323 | |||||||
chr11:77741515 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0305 |
2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.373-579G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741515 | |||||||
chr11:77741518 | T | A | 23 | a0001c0002t0003g0018 a0001c0002t0003g0053 a0001c0002t0003g0054 others(20): Show |
23 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.373-582A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741518 | |||||||
chr11:77741552 | AT | A | 73 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(70): Show |
73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.373-617delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741552 | |||||||
chr11:77741596 | T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.373-660A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741596 | |||||||
chr11:77741615 | C | T | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.373-679G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741615 | |||||||
chr11:77741745 | T | C | 29 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0212 others(26): Show |
29 | HG00673.hp2 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.373-809A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741745 | |||||||
chr11:77741903 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.373-967C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741903 | |||||||
chr11:77742067 | C | G | 82 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.373-1131G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742067 | |||||||
chr11:77742240 | G | A | 3 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 |
3 | NA18747.hp2 NA18950.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.373-1304C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742240 | |||||||
chr11:77742322 | C | T | 75 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(72): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.373-1386G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742322 | |||||||
chr11:77742341 | G | A | 22 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.373-1405C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742341 | |||||||
chr11:77742355 | C | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-1419G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742355 | |||||||
chr11:77742441 | A | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-1505T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742441 | |||||||
chr11:77742624 | T | G | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.373-1688A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742624 | |||||||
chr11:77742671 | C | T | 306 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(303): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.373-1735G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742671 | |||||||
chr11:77742754 | G | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1818C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742754 | |||||||
chr11:77742878 | G | A | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.373-1942C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742878 | |||||||
chr11:77743028 | C | T | 1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.373-2092G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743028 | |||||||
chr11:77743031 | C | T | 155 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.373-2095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743031 | |||||||
chr11:77743034 | C | T | 1 | a0001c0010t0001g0340 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.373-2098G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743034 | |||||||
chr11:77743035 | A | C | 1 | a0001c0010t0001g0340 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.373-2099T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743035 | |||||||
chr11:77743191 | C | G | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.373-2255G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743191 | |||||||
chr11:77743212 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.373-2276T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743212 | |||||||
chr11:77743237 | T | C | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.373-2301A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743237 | |||||||
chr11:77743312 | G | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0100 others(80): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.373-2376C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743312 | |||||||
chr11:77743330 | G | A | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.373-2394C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743330 | |||||||
chr11:77743568 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.373-2632T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743568 | |||||||
chr11:77744027 | A | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.372+3009T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744027 | |||||||
chr11:77744119 | C | T | 1 | a0001c0010t0001g0340 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+2917G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744119 | |||||||
chr11:77744121 | C | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+2915G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744121 | |||||||
chr11:77744384 | G | A | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2652C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744384 | |||||||
chr11:77744385 | C | T | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.372+2651G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744385 | |||||||
chr11:77744448 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.372+2588C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744448 | |||||||
chr11:77744497 | A | G | 238 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.372+2539T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744497 | |||||||
chr11:77744538 | A | G | 157 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(154): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.372+2498T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744538 | |||||||
chr11:77744651 | C | G | 1 | a0001c0001t0004g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+2385G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744651 | |||||||
chr11:77744693 | T | C | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+2343A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744693 | |||||||
chr11:77744859 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.372+2177T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744859 | |||||||
chr11:77744998 | G | C | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.372+2038C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744998 | |||||||
chr11:77745000 | T | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2036A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745000 | |||||||
chr11:77745056 | A | AT | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.372+1979dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745056 | |||||||
chr11:77745087 | A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.372+1949T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745087 | |||||||
chr11:77745090 | G | C | 1 | a0001c0001t0004g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+1946C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745090 | |||||||
chr11:77745115 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.372+1921G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745115 | |||||||
chr11:77745298 | T | C | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+1738A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745298 | |||||||
chr11:77745328 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.372+1708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745328 | |||||||
chr11:77745509 | A | ATT | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+1525_372+1526d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745509 | |||||||
chr11:77745509 | AT | A | 26 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(23): Show |
26 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.372+1526delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745509 | |||||||
chr11:77745592 | C | T | 2 | a0001c0001t0009g0243 a0001c0001t0009g0244 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.372+1444G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745592 | |||||||
chr11:77745741 | T | C | 21 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(18): Show |
21 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.372+1295A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745741 | |||||||
chr11:77745764 | T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.372+1272A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745764 | |||||||
chr11:77745794 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.372+1242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745794 | |||||||
chr11:77745828 | G | C | 1 | a0001c0010t0001g0340 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+1208C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745828 | |||||||
chr11:77745829 | C | G | 1 | a0001c0010t0001g0340 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+1207G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745829 | |||||||
chr11:77745861 | A | G | 54 | a0001c0001t0006g0121 a0001c0001t0009g0242 a0001c0001t0009g0243 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.372+1175T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745861 | |||||||
chr11:77745889 | T | A | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.372+1147A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745889 | |||||||
chr11:77746007 | A | G | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.372+1029T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746007 | |||||||
chr11:77746348 | C | A | 1 | a0001c0001t0001g0318 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.372+688G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746348 | |||||||
chr11:77746356 | T | C | 2 | a0002c0003t0002g0203 a0002c0003t0002g0230 |
2 | NA18955.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.372+680A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746356 | |||||||
chr11:77746490 | A | G | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.372+546T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746490 | |||||||
chr11:77746571 | C | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+465G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746571 | |||||||
chr11:77746666 | C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+370G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746666 | |||||||
chr11:77746712 | A | G | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.372+324T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746712 | |||||||
chr11:77746780 | C | T | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+256G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746780 | |||||||
chr11:77747310 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.280-182C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747310 | |||||||
chr11:77747754 | T | C | 13 | a0001c0002t0003g0033 a0001c0002t0003g0035 a0001c0002t0003g0036 others(10): Show |
13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.280-626A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747754 | |||||||
chr11:77747831 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280-703C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747831 | |||||||
chr11:77747862 | G | T | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.280-734C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747862 | |||||||
chr11:77747978 | C | T | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.280-850G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747978 | |||||||
chr11:77748216 | C | CT | 8 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(5): Show |
8 | HG01243.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-1089dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748216 | |||||||
chr11:77748216 | CT | C | 84 | a0001c0001t0001g0279 a0001c0001t0001g0286 a0001c0001t0004g0100 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.280-1089delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748216 | |||||||
chr11:77748228 | T | C | 1 | a0001c0001t0047g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-1100A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748228 | |||||||
chr11:77748229 | C | T | 1 | a0001c0001t0047g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-1101G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748229 | |||||||
chr11:77748349 | C | T | 70 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.280-1221G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748349 | |||||||
chr11:77748365 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.280-1237A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748365 | |||||||
chr11:77748370 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748370 | |||||||
chr11:77748590 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1462G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748590 | |||||||
chr11:77748684 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0057g0278 |
2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.280-1556C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748684 | |||||||
chr11:77748841 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-1713C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748841 | |||||||
chr11:77749023 | G | A | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280-1895C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749023 | |||||||
chr11:77749234 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280-2106A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749234 | |||||||
chr11:77749277 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-2149A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749277 | |||||||
chr11:77749325 | A | G | 1 | a0001c0002t0003g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.280-2197T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749325 | |||||||
chr11:77749569 | A | G | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.280-2441T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749569 | |||||||
chr11:77749702 | T | C | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.280-2574A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749702 | |||||||
chr11:77749716 | C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-2588G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749716 | |||||||
chr11:77749969 | G | A | 1 | a0001c0002t0003g0028 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.280-2841C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749969 | |||||||
chr11:77750007 | C | A | 261 | a0001c0001t0001g0264 a0001c0001t0002g0003 a0001c0001t0002g0004 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.280-2879G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750007 | |||||||
chr11:77750014 | T | C | 2 | a0002c0003t0002g0204 a0002c0003t0002g0205 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.280-2886A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750014 | |||||||
chr11:77750099 | T | TA | 12 | a0001c0001t0001g0286 a0001c0001t0004g0187 a0001c0002t0003g0022 others(9): Show |
12 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-2972dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750099 | |||||||
chr11:77750121 | T | C | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0051g0182 |
3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.280-2993A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750121 | |||||||
chr11:77750268 | T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280-3140A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750268 | |||||||
chr11:77750302 | T | C | 4 | a0001c0001t0013g0271 a0001c0001t0013g0272 a0001c0001t0013g0273 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-3174A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750302 | |||||||
chr11:77750502 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.280-3374A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750502 | |||||||
chr11:77750608 | T | C | 1 | a0001c0001t0005g0254 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.280-3480A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750608 | |||||||
chr11:77750839 | T | C | 1 | a0001c0001t0004g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.280-3711A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750839 | |||||||
chr11:77751348 | C | T | 2 | a0001c0002t0018g0046 a0012c0008t0003g0034 |
2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280-4220G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751348 | |||||||
chr11:77751377 | A | C | 1 | a0001c0001t0043g0153 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.280-4249T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751377 | |||||||
chr11:77751429 | C | T | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.280-4301G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751429 | |||||||
chr11:77751457 | CAA | C | 75 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.280-4331_280-4330d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751457 | |||||||
chr11:77751637 | G | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.280-4509C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751637 | |||||||
chr11:77751693 | A | G | 1 | a0001c0002t0003g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-4565T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751693 | |||||||
chr11:77751747 | C | T | 74 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.280-4619G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751747 | |||||||
chr11:77752102 | C | T | 1 | a0001c0001t0067g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.280-4974G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752102 | |||||||
chr11:77752183 | C | T | 11 | a0001c0001t0004g0143 a0001c0001t0004g0147 a0001c0001t0004g0148 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-5055G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752183 | |||||||
chr11:77752332 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5204C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752332 | |||||||
chr11:77752410 | C | A | 2 | a0001c0002t0014g0009 a0001c0002t0014g0011 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.280-5282G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752410 | |||||||
chr11:77752541 | A | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-5413T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752541 | |||||||
chr11:77752679 | C | T | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.280-5551G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752679 | |||||||
chr11:77752946 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-5818A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752946 | |||||||
chr11:77752967 | T | A | 1 | a0001c0001t0040g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.280-5839A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752967 | |||||||
chr11:77753108 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-5980A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753108 | |||||||
chr11:77753108 | T | G | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.280-5980A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753108 | |||||||
chr11:77753325 | C | T | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6197G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753325 | |||||||
chr11:77753381 | T | C | 7 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(4): Show |
7 | NA18963.hp1 NA18965.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-6253A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753381 | |||||||
chr11:77753485 | G | A | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6357C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753485 | |||||||
chr11:77753525 | G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-6397C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753525 | |||||||
chr11:77753526 | GACGGTTT others(2): Show |
G | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-6407_280-6399d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753526 | |||||||
chr11:77753686 | G | C | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.280-6558C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753686 | |||||||
chr11:77753695 | C | T | 1 | a0001c0002t0003g0025 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.280-6567G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753695 | |||||||
chr11:77753721 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-6593C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753721 | |||||||
chr11:77753789 | A | G | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6661T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753789 | |||||||
chr11:77753849 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.280-6721A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753849 | |||||||
chr11:77753865 | T | A | 1 | a0001c0002t0003g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280-6737A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753865 | |||||||
chr11:77753891 | C | T | 78 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.280-6763G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753891 | |||||||
chr11:77753987 | G | A | 2 | a0001c0001t0009g0243 a0001c0001t0009g0244 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.280-6859C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753987 | |||||||
chr11:77754366 | C | T | 1 | a0001c0001t0004g0103 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.280-7238G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754366 | |||||||
chr11:77754408 | C | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7280G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754408 | |||||||
chr11:77754451 | A | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7323T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754451 | |||||||
chr11:77754584 | A | G | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280-7456T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754584 | |||||||
chr11:77754757 | C | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-7629G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754757 | |||||||
chr11:77754762 | A | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-7634T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754762 | |||||||
chr11:77754831 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.280-7703A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754831 | |||||||
chr11:77754835 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-7707C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754835 | |||||||
chr11:77754839 | C | A | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.280-7711G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754839 | |||||||
chr11:77754949 | C | A | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.280-7821G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754949 | |||||||
chr11:77755289 | G | A | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.280-8161C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755289 | |||||||
chr11:77755304 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280-8176A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755304 | |||||||
chr11:77755345 | A | C | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-8217T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755345 | |||||||
chr11:77755432 | T | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.280-8304A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755432 | |||||||
chr11:77755434 | G | T | 1 | a0001c0001t0001g0287 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.280-8306C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755434 | |||||||
chr11:77755584 | A | AT | 162 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0100 others(159): Show |
162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.280-8457dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755584 | |||||||
chr11:77755584 | ATT | A | 17 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(14): Show |
17 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-8458_280-8457d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755584 | |||||||
chr11:77755605 | A | G | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.280-8477T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755605 | |||||||
chr11:77755657 | G | A | 1 | a0001c0002t0003g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-8529C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755657 | |||||||
chr11:77755726 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-8598G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755726 | |||||||
chr11:77755740 | T | C | 163 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0100 others(160): Show |
163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.280-8612A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755740 | |||||||
chr11:77755821 | G | A | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.280-8693C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755821 | |||||||
chr11:77755855 | G | A | 1 | a0001c0002t0003g0077 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.280-8727C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755855 | |||||||
chr11:77756028 | A | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+8570T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756028 | |||||||
chr11:77756052 | A | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+8546T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756052 | |||||||
chr11:77756358 | C | CA | 19 | a0001c0001t0002g0119 a0001c0001t0004g0164 a0001c0001t0004g0195 others(16): Show |
19 | HG01074.hp1 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.279+8239dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756358 | |||||||
chr11:77756362 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0290 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.279+8236T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756362 | |||||||
chr11:77756528 | T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+8070A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756528 | |||||||
chr11:77756975 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.279+7623A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756975 | |||||||
chr11:77756991 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.279+7607A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756991 | |||||||
chr11:77757021 | C | T | 3 | a0001c0002t0010g0013 a0001c0002t0033g0012 a0011c0018t0032g0014 |
3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.279+7577G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757021 | |||||||
chr11:77757043 | C | A | 70 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.279+7555G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757043 | |||||||
chr11:77757354 | C | T | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279+7244G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757354 | |||||||
chr11:77757507 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.279+7091C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757507 | |||||||
chr11:77757666 | A | G | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.279+6932T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757666 | |||||||
chr11:77757937 | C | T | 1 | a0001c0002t0003g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.279+6661G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757937 | |||||||
chr11:77758003 | T | C | 1 | a0002c0003t0050g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.279+6595A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758003 | |||||||
chr11:77758140 | GA | G | 84 | a0001c0001t0001g0318 a0001c0001t0002g0132 a0001c0001t0004g0100 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.279+6457delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758140 | |||||||
chr11:77758321 | A | G | 1 | a0001c0001t0066g0173 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.279+6277T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758321 | |||||||
chr11:77758381 | C | T | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.279+6217G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758381 | |||||||
chr11:77758472 | G | C | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.279+6126C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758472 | |||||||
chr11:77758559 | T | G | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.279+6039A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758559 | |||||||
chr11:77758621 | A | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+5977T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758621 | |||||||
chr11:77758858 | AC | A | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.279+5739delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758858 | |||||||
chr11:77759022 | A | C | 78 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.279+5576T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759022 | |||||||
chr11:77759121 | A | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.279+5477T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759121 | |||||||
chr11:77759184 | T | C | 1 | a0001c0001t0005g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.279+5414A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759184 | |||||||
chr11:77759298 | C | T | 1 | a0002c0003t0002g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.279+5300G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759298 | |||||||
chr11:77759332 | G | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279+5266C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759332 | |||||||
chr11:77759482 | G | A | 1 | a0001c0001t0008g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.279+5116C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759482 | |||||||
chr11:77759541 | A | T | 75 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(72): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.279+5057T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759541 | |||||||
chr11:77759553 | G | A | 4 | a0001c0001t0013g0271 a0001c0001t0013g0272 a0001c0001t0013g0273 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+5045C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759553 | |||||||
chr11:77759598 | C | A | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.279+5000G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759598 | |||||||
chr11:77759728 | G | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279+4870C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759728 | |||||||
chr11:77759768 | C | G | 3 | a0001c0002t0003g0066 a0001c0002t0003g0072 a0001c0002t0003g0076 |
3 | NA18965.hp1 NA18967.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.279+4830G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759768 | |||||||
chr11:77759855 | T | TA | 245 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.279+4742dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759855 | |||||||
chr11:77759855 | TA | T | 77 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(74): Show |
77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.279+4742delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759855 | |||||||
chr11:77759906 | T | C | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0117 |
3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.279+4692A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759906 | |||||||
chr11:77759997 | C | T | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.279+4601G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759997 | |||||||
chr11:77760102 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.279+4496G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760102 | |||||||
chr11:77760167 | G | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.279+4431C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760167 | |||||||
chr11:77760627 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279+3971A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760627 | |||||||
chr11:77760781 | G | T | 25 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(22): Show |
25 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+3817C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760781 | |||||||
chr11:77760856 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+3742T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760856 | |||||||
chr11:77760899 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.279+3699G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760899 | |||||||
chr11:77761076 | C | G | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.279+3522G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761076 | |||||||
chr11:77761093 | C | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+3505G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761093 | |||||||
chr11:77761123 | T | G | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.279+3475A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761123 | |||||||
chr11:77761130 | G | A | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.279+3468C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761130 | |||||||
chr11:77761193 | C | A | 1 | a0001c0001t0002g0108 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+3405G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761193 | |||||||
chr11:77761504 | C | CT | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+3093_279+3094i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761504 | |||||||
chr11:77761574 | T | C | 2 | a0001c0001t0038g0170 a0001c0001t0039g0166 |
2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.279+3024A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761574 | |||||||
chr11:77761577 | G | A | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.279+3021C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761577 | |||||||
chr11:77761828 | A | ACTTTTT | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2769_279+2770i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77761828 | A | AT | 245 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.279+2769dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77761828 | A | ATT | 15 | a0001c0001t0001g0089 a0001c0001t0001g0288 a0001c0001t0001g0312 others(12): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.279+2768_279+2769d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77761828 | A | ATTTTT | 7 | a0001c0002t0003g0041 a0001c0002t0003g0078 a0001c0002t0010g0013 others(4): Show |
7 | HG01069.hp2 HG01074.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2765_279+2769d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77761828 | A | ATTTTTT | 52 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0022 others(49): Show |
52 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+2764_279+2769d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77761828 | A | ATTTTTTT | 19 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 others(16): Show |
19 | HG00423.hp2 HG00597.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.279+2763_279+2769d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | |||||||
chr11:77762017 | C | A | 17 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(14): Show |
17 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.279+2581G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762017 | |||||||
chr11:77762022 | C | CTTTTCTT | 23 | a0001c0001t0004g0157 a0001c0001t0005g0252 a0001c0001t0005g0254 others(20): Show |
23 | HG01074.hp2 HG01433.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.279+2569_279+2575d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762022 | |||||||
chr11:77762027 | C | CTTTTT | 8 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0023 others(5): Show |
8 | HG02280.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+2566_279+2570d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTT | 61 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.279+2565_279+2570d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(1): Show |
66 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0001t0004g0133 others(63): Show |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(2): Show |
11 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(8): Show |
11 | HG00609.hp1 HG02080.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(3): Show |
1 | a0001c0001t0004g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(6): Show |
1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(7): Show |
22 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0111 others(19): Show |
22 | HG02055.hp1 HG02486.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(8): Show |
5 | a0001c0001t0002g0108 a0001c0001t0002g0128 a0001c0001t0006g0122 others(2): Show |
5 | HG02647.hp2 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTC others(9): Show |
1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTT | 8 | a0001c0001t0005g0038 a0001c0002t0003g0036 a0001c0002t0003g0043 others(5): Show |
8 | HG00733.hp2 HG02071.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+2564_279+2570d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762027 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.279+2552_279+2570d others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | |||||||
chr11:77762033 | T | TC | 41 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.279+2564_279+2565i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762033 | |||||||
chr11:77762034 | T | C | 1 | a0002c0003t0002g0235 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.279+2564A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762034 | |||||||
chr11:77762035 | T | C | 1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.279+2563A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762035 | |||||||
chr11:77762089 | G | C | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+2509C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762089 | |||||||
chr11:77762164 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+2434A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762164 | |||||||
chr11:77762278 | A | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+2320T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762278 | |||||||
chr11:77762338 | C | T | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.279+2260G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762338 | |||||||
chr11:77762364 | T | C | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.279+2234A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762364 | |||||||
chr11:77762460 | T | C | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.279+2138A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762460 | |||||||
chr11:77762552 | G | A | 2 | a0002c0003t0002g0099 a0002c0003t0002g0228 |
2 | HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.279+2046C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762552 | |||||||
chr11:77762753 | T | C | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.279+1845A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762753 | |||||||
chr11:77763040 | ATAAAAGA others(1): Show |
A | 10 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(7): Show |
10 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1550_279+1557d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763040 | |||||||
chr11:77763048 | T | C | 7 | a0001c0002t0003g0048 a0001c0002t0003g0052 a0001c0002t0003g0055 others(4): Show |
7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+1550A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763048 | |||||||
chr11:77763068 | C | G | 7 | a0001c0002t0010g0013 a0001c0002t0016g0005 a0001c0002t0016g0008 others(4): Show |
7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+1530G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763068 | |||||||
chr11:77763116 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1482C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763116 | |||||||
chr11:77763290 | C | T | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1308G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763290 | |||||||
chr11:77763291 | G | A | 2 | a0001c0001t0009g0243 a0001c0001t0009g0244 |
2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.279+1307C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763291 | |||||||
chr11:77763340 | T | TA | 159 | a0001c0001t0001g0264 a0001c0001t0002g0003 a0001c0001t0002g0004 others(156): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.279+1257dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763340 | |||||||
chr11:77763340 | TA | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(6): Show |
9 | HG01256.hp1 HG01515.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.279+1257delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763340 | |||||||
chr11:77763464 | G | C | 2 | a0001c0001t0008g0269 a0001c0001t0008g0270 |
2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.279+1134C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763464 | |||||||
chr11:77764122 | G | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+476C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764122 | |||||||
chr11:77764358 | G | A | 13 | a0001c0002t0003g0033 a0001c0002t0003g0035 a0001c0002t0003g0036 others(10): Show |
13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.279+240C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764358 | |||||||
chr11:77764461 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+137G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764461 | |||||||
chr11:77764983 | T | C | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.188-294A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77764983 | |||||||
chr11:77765028 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-339G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765028 | |||||||
chr11:77765135 | TA | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-447delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765135 | |||||||
chr11:77765638 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-949G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765638 | |||||||
chr11:77765931 | A | C | 3 | a0001c0001t0005g0254 a0001c0001t0025g0259 a0009c0014t0005g0258 |
3 | NA18942.hp1 NA18977.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.188-1242T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765931 | |||||||
chr11:77765991 | G | A | 9 | a0001c0002t0003g0048 a0001c0002t0003g0050 a0001c0002t0003g0052 others(6): Show |
9 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-1302C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765991 | |||||||
chr11:77766133 | T | C | 4 | a0002c0003t0002g0345 a0002c0003t0002g0346 a0002c0003t0002g0347 others(1): Show |
4 | HG01891.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-1444A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766133 | |||||||
chr11:77766138 | C | CA | 7 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0002t0010g0013 others(4): Show |
7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-1450dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766138 | |||||||
chr11:77766154 | G | GT | 73 | a0001c0001t0001g0288 a0001c0001t0005g0038 a0001c0002t0003g0018 others(70): Show |
73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.188-1466dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766154 | |||||||
chr11:77766299 | G | A | 1 | a0001c0002t0003g0052 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.188-1610C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766299 | |||||||
chr11:77766697 | A | C | 1 | a0002c0003t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.188-2008T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766697 | |||||||
chr11:77766706 | A | C | 1 | a0002c0003t0050g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.188-2017T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766706 | |||||||
chr11:77766783 | T | C | 85 | a0001c0001t0001g0277 a0001c0001t0001g0290 a0001c0001t0001g0308 others(82): Show |
85 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.188-2094A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766783 | |||||||
chr11:77766825 | GTTT | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-2139_188-2137d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766825 | |||||||
chr11:77766867 | C | T | 2 | a0001c0001t0002g0108 a0001c0002t0003g0072 |
2 | NA18967.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.188-2178G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766867 | |||||||
chr11:77766911 | A | G | 265 | a0001c0001t0001g0264 a0001c0001t0001g0318 a0001c0001t0001g0327 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.188-2222T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766911 | |||||||
chr11:77766938 | T | C | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.188-2249A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766938 | |||||||
chr11:77766953 | A | G | 2 | a0001c0001t0006g0121 a0003c0005t0049g0202 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-2264T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766953 | |||||||
chr11:77767063 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-2374C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767063 | |||||||
chr11:77767123 | C | T | 1 | a0002c0003t0002g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-2434G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767123 | |||||||
chr11:77767163 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-2474A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767163 | |||||||
chr11:77767424 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-2735A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767424 | |||||||
chr11:77767673 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-2984A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767673 | |||||||
chr11:77767734 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3045G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767734 | |||||||
chr11:77767741 | T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-3052A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767741 | |||||||
chr11:77767775 | T | C | 19 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(16): Show |
19 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-3086A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767775 | |||||||
chr11:77768020 | T | C | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-3331A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768020 | |||||||
chr11:77768045 | C | T | 52 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(49): Show |
52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-3356G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768045 | |||||||
chr11:77768143 | A | G | 9 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(6): Show |
9 | HG02602.hp2 HG03654.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-3454T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768143 | |||||||
chr11:77768161 | C | CT | 44 | a0001c0001t0001g0087 a0001c0001t0001g0276 a0001c0001t0001g0282 others(41): Show |
44 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.188-3473dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | |||||||
chr11:77768161 | C | CTT | 22 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0006g0118 others(19): Show |
22 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.188-3474_188-3473d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | |||||||
chr11:77768161 | C | CTTT | 58 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(55): Show |
58 | HG00280.hp2 HG00423.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.188-3475_188-3473d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | |||||||
chr11:77768161 | C | CTTTT | 9 | a0001c0002t0003g0020 a0001c0002t0003g0054 a0001c0002t0003g0063 others(6): Show |
9 | HG00408.hp2 HG00597.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-3476_188-3473d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | |||||||
chr11:77768193 | C | T | 3 | a0001c0002t0010g0013 a0001c0002t0033g0012 a0011c0018t0032g0014 |
3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.188-3504G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768193 | |||||||
chr11:77768219 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3530C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768219 | |||||||
chr11:77768248 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3559A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768248 | |||||||
chr11:77768373 | G | A | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.188-3684C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768373 | |||||||
chr11:77768407 | G | A | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.188-3718C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768407 | |||||||
chr11:77768412 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.188-3723C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768412 | |||||||
chr11:77768453 | G | A | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.188-3764C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768453 | |||||||
chr11:77768792 | T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-4103A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768792 | |||||||
chr11:77768873 | C | A | 1 | a0002c0003t0002g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.188-4184G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768873 | |||||||
chr11:77768991 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-4302T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768991 | |||||||
chr11:77769017 | G | A | 4 | a0001c0002t0029g0017 a0002c0003t0012g0220 a0002c0003t0021g0209 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-4328C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769017 | |||||||
chr11:77769067 | T | C | 1 | a0001c0001t0011g0172 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.188-4378A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769067 | |||||||
chr11:77769073 | T | C | 1 | a0001c0001t0039g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.188-4384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769073 | |||||||
chr11:77769119 | G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-4430C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769119 | |||||||
chr11:77769174 | C | G | 1 | a0001c0001t0011g0172 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.188-4485G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769174 | |||||||
chr11:77769204 | C | T | 3 | a0001c0002t0003g0082 a0001c0002t0003g0083 a0001c0002t0003g0084 |
3 | HG02523.hp1 NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.188-4515G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769204 | |||||||
chr11:77769403 | A | G | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.188-4714T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769403 | |||||||
chr11:77769498 | T | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-4809A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769498 | |||||||
chr11:77769897 | T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-5208A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769897 | |||||||
chr11:77770153 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-5464C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770153 | |||||||
chr11:77770387 | G | A | 2 | a0001c0001t0006g0121 a0003c0005t0049g0202 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-5698C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770387 | |||||||
chr11:77770510 | T | C | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.188-5821A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770510 | |||||||
chr11:77770686 | C | T | 1 | a0002c0003t0002g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.188-5997G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770686 | |||||||
chr11:77770763 | A | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-6074T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770763 | |||||||
chr11:77770895 | G | A | 4 | a0001c0001t0013g0271 a0001c0001t0013g0272 a0001c0001t0013g0273 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-6206C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770895 | |||||||
chr11:77771001 | T | C | 1 | a0002c0003t0002g0219 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.188-6312A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771001 | |||||||
chr11:77771308 | G | A | 1 | a0001c0001t0009g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.188-6619C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771308 | |||||||
chr11:77771608 | C | G | 6 | a0001c0001t0007g0151 a0001c0001t0007g0162 a0001c0001t0007g0163 others(3): Show |
6 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-6919G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771608 | |||||||
chr11:77771646 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.188-6957G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771646 | |||||||
chr11:77771728 | A | G | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-7039T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771728 | |||||||
chr11:77771737 | C | T | 1 | a0001c0001t0007g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.188-7048G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771737 | |||||||
chr11:77771876 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-7187A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771876 | |||||||
chr11:77771934 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188-7245A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771934 | |||||||
chr11:77772084 | G | A | 1 | a0001c0001t0001g0339 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.188-7395C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772084 | |||||||
chr11:77772417 | G | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-7728C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772417 | |||||||
chr11:77772831 | A | G | 1 | a0001c0001t0053g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.188-8142T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772831 | |||||||
chr11:77772848 | G | GA | 141 | a0001c0001t0001g0294 a0001c0001t0001g0311 a0001c0001t0001g0318 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.188-8160dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | |||||||
chr11:77772848 | G | GAA | 19 | a0001c0001t0002g0112 a0001c0001t0002g0126 a0001c0001t0002g0131 others(16): Show |
19 | HG00733.hp1 HG01074.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-8161_188-8160d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | |||||||
chr11:77772848 | GA | G | 70 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(67): Show |
70 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.188-8160delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | |||||||
chr11:77773272 | C | T | 2 | a0001c0001t0006g0123 a0001c0001t0006g0127 |
2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.188-8583G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773272 | |||||||
chr11:77773339 | C | T | 9 | a0001c0001t0001g0274 a0001c0001t0001g0334 a0001c0001t0001g0335 others(6): Show |
9 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-8650G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773339 | |||||||
chr11:77773413 | G | A | 7 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0093 others(4): Show |
7 | HG00323.hp1 HG00741.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-8724C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773413 | |||||||
chr11:77773670 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188-8981A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773670 | |||||||
chr11:77773689 | T | C | 261 | a0001c0001t0001g0264 a0001c0001t0002g0003 a0001c0001t0002g0004 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.188-9000A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773689 | |||||||
chr11:77773701 | C | T | 3 | a0001c0001t0022g0140 a0001c0001t0022g0141 a0001c0001t0054g0142 |
3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188-9012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773701 | |||||||
chr11:77773868 | C | T | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-9179G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773868 | |||||||
chr11:77774155 | T | C | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.188-9466A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774155 | |||||||
chr11:77774164 | T | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.188-9475A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774164 | |||||||
chr11:77774231 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.188-9542G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774231 | |||||||
chr11:77774395 | G | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-9706C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774395 | |||||||
chr11:77774573 | A | AAAAT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
19 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-9888_188-9885d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | |||||||
chr11:77774573 | AAAAT | A | 137 | a0001c0001t0001g0309 a0001c0001t0002g0003 a0001c0001t0002g0004 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.188-9888_188-9885d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | |||||||
chr11:77774573 | AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0264 a0001c0001t0004g0180 a0001c0001t0006g0122 others(4): Show |
7 | HG01074.hp1 HG03098.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-9892_188-9885d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | |||||||
chr11:77774573 | AAAATAAA others(5): Show |
A | 3 | a0001c0002t0010g0350 a0001c0002t0010g0351 a0001c0002t0033g0012 |
3 | HG02055.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-9896_188-9885d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | |||||||
chr11:77774573 | AAAATAAA others(9): Show |
A | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-9900_188-9885d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | |||||||
chr11:77774617 | T | A | 3 | a0001c0001t0001g0294 a0001c0001t0004g0157 a0001c0001t0004g0167 |
3 | HG01123.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.188-9928A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774617 | |||||||
chr11:77774677 | A | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-9988T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774677 | |||||||
chr11:77774721 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188-10032C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774721 | |||||||
chr11:77774773 | C | CT | 78 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(75): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.188-10085dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774773 | |||||||
chr11:77774826 | G | T | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10137C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774826 | |||||||
chr11:77774924 | G | C | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10235C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774924 | |||||||
chr11:77774925 | C | G | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10236G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774925 | |||||||
chr11:77775204 | C | T | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.188-10515G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775204 | |||||||
chr11:77775324 | A | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-10635T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775324 | |||||||
chr11:77775434 | G | T | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10745C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775434 | |||||||
chr11:77775679 | A | T | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10990T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775679 | |||||||
chr11:77775811 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-11122A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775811 | |||||||
chr11:77775811 | T | G | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.188-11122A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775811 | |||||||
chr11:77775812 | A | T | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11123T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775812 | |||||||
chr11:77775940 | T | C | 13 | a0001c0002t0003g0033 a0001c0002t0003g0035 a0001c0002t0003g0036 others(10): Show |
13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-11251A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775940 | |||||||
chr11:77776117 | A | G | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-11428T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776117 | |||||||
chr11:77776204 | C | A | 2 | a0001c0001t0004g0101 a0001c0001t0004g0102 |
2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.188-11515G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776204 | |||||||
chr11:77776229 | CA | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-11541delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776229 | |||||||
chr11:77776323 | C | G | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-11634G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776323 | |||||||
chr11:77776371 | C | A | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11682G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776371 | |||||||
chr11:77776372 | A | T | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11683T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776372 | |||||||
chr11:77776375 | T | C | 1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11686A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776375 | |||||||
chr11:77776698 | C | A | 1 | a0001c0002t0014g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188-12009G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776698 | |||||||
chr11:77777011 | T | A | 349 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(346): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.188-12322A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777011 | |||||||
chr11:77777029 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-12340C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777029 | |||||||
chr11:77777033 | G | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.188-12344C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777033 | |||||||
chr11:77777034 | A | T | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.188-12345T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777034 | |||||||
chr11:77777041 | C | A | 1 | a0002c0003t0050g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.188-12352G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777041 | |||||||
chr11:77777056 | A | T | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0290 others(1): Show |
4 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-12367T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777056 | |||||||
chr11:77777132 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-12443T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777132 | |||||||
chr11:77777384 | G | A | 3 | a0002c0003t0002g0216 a0002c0003t0002g0221 a0002c0003t0002g0229 |
3 | HG01070.hp2 HG01168.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.188-12695C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777384 | |||||||
chr11:77777448 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.188-12759G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777448 | |||||||
chr11:77777763 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13074G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777763 | |||||||
chr11:77777779 | G | A | 69 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-13090C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777779 | |||||||
chr11:77777937 | G | C | 1 | a0002c0003t0002g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.188-13248C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777937 | |||||||
chr11:77777950 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188-13261A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777950 | |||||||
chr11:77778095 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-13406A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778095 | |||||||
chr11:77778115 | A | AGGAGGAG others(102): Show |
1 | a0001c0002t0031g0075 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(104): Show |
1 | a0001c0001t0004g0183 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(104): Show |
1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(102): Show |
1 | a0001c0001t0002g0110 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(103): Show |
325 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(322): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.188-13427_188-1342 others(114): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(104): Show |
1 | a0001c0001t0053g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(102): Show |
1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(105): Show |
1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.188-13427_188-1342 others(116): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(104): Show |
15 | a0001c0001t0001g0276 a0001c0001t0001g0318 a0001c0001t0002g0115 others(12): Show |
15 | HG01358.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778115 | A | AGGAGGAG others(105): Show |
1 | a0001c0001t0002g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(116): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | |||||||
chr11:77778118 | A | AGGAGGGG others(104): Show |
1 | a0001c0001t0001g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188-13430_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778118 | |||||||
chr11:77778118 | A | AGGAGGGG others(107): Show |
1 | a0001c0001t0054g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-13430_188-1342 others(118): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778118 | |||||||
chr11:77778144 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13455C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778144 | |||||||
chr11:77778179 | AGGGGAGG others(4): Show |
A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13501_188-1349 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778179 | |||||||
chr11:77778201 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-13512C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778201 | |||||||
chr11:77778219 | G | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-13530C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778219 | |||||||
chr11:77778227 | T | G | 1 | a0001c0002t0003g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.188-13538A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778227 | |||||||
chr11:77778329 | G | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.188-13640C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778329 | |||||||
chr11:77778430 | T | G | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0126 |
3 | NA18963.hp1 NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.188-13741A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778430 | |||||||
chr11:77778470 | G | A | 1 | a0001c0001t0004g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.188-13781C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778470 | |||||||
chr11:77778562 | T | G | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-13873A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778562 | |||||||
chr11:77778679 | C | T | 72 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.188-13990G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778679 | |||||||
chr11:77778704 | T | G | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-14015A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778704 | |||||||
chr11:77778805 | C | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-14116G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778805 | |||||||
chr11:77779185 | C | T | 2 | a0001c0001t0004g0136 a0001c0001t0042g0174 |
2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.188-14496G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779185 | |||||||
chr11:77779349 | A | AGCCG | 6 | a0001c0001t0007g0151 a0001c0001t0007g0162 a0001c0001t0007g0163 others(3): Show |
6 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-14661_188-1466 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779349 | |||||||
chr11:77779384 | A | AT | 20 | a0001c0001t0001g0277 a0001c0001t0001g0287 a0001c0001t0001g0342 others(17): Show |
20 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.188-14696dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | |||||||
chr11:77779384 | A | ATT | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-14697_188-1469 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | |||||||
chr11:77779384 | A | T | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.188-14695T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | |||||||
chr11:77779384 | AT | A | 6 | a0001c0001t0001g0320 a0001c0001t0004g0143 a0001c0001t0004g0167 others(3): Show |
6 | HG01070.hp2 HG01081.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-14696delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | |||||||
chr11:77779385 | T | A | 2 | a0001c0001t0001g0334 a0001c0001t0007g0151 |
2 | HG00544.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.188-14696A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779385 | |||||||
chr11:77779404 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188-14715A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779404 | |||||||
chr11:77779405 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188-14716C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779405 | |||||||
chr11:77779804 | T | C | 265 | a0001c0001t0001g0264 a0001c0001t0001g0276 a0001c0001t0001g0277 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.188-15115A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779804 | |||||||
chr11:77779912 | G | A | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-15223C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779912 | |||||||
chr11:77779957 | C | G | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.188-15268G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779957 | |||||||
chr11:77780035 | G | A | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.188-15346C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780035 | |||||||
chr11:77780210 | T | C | 4 | a0002c0004t0002g0231 a0002c0004t0002g0233 a0002c0004t0002g0234 others(1): Show |
4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15521A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780210 | |||||||
chr11:77780366 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.188-15677T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780366 | |||||||
chr11:77780548 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15859C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780548 | |||||||
chr11:77780599 | G | A | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.188-15910C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780599 | |||||||
chr11:77780682 | G | A | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-15993C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780682 | |||||||
chr11:77780757 | A | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-16068T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780757 | |||||||
chr11:77780818 | C | A | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-16129G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780818 | |||||||
chr11:77780824 | C | CA | 153 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(150): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.188-16136dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | |||||||
chr11:77780824 | C | CAA | 109 | a0001c0001t0001g0097 a0001c0001t0001g0301 a0001c0001t0002g0108 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.188-16137_188-1613 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | |||||||
chr11:77780824 | C | CAAA | 6 | a0001c0001t0002g0117 a0001c0001t0009g0243 a0001c0001t0009g0244 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-16138_188-1613 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | |||||||
chr11:77780824 | CA | C | 7 | a0001c0002t0010g0013 a0001c0002t0016g0005 a0001c0002t0016g0008 others(4): Show |
7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-16136delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | |||||||
chr11:77780854 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188-16165T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780854 | |||||||
chr11:77781100 | T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-16411A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781100 | |||||||
chr11:77781103 | T | C | 1 | a0001c0002t0003g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-16414A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781103 | |||||||
chr11:77781104 | C | CT | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-16416dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781104 | |||||||
chr11:77781113 | T | G | 2 | a0003c0005t0020g0199 a0003c0005t0020g0200 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.188-16424A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781113 | |||||||
chr11:77781114 | T | A | 3 | a0001c0002t0035g0057 a0003c0005t0020g0199 a0003c0005t0020g0200 |
3 | HG02451.hp2 HG03041.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.188-16425A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781114 | |||||||
chr11:77781180 | A | C | 1 | a0001c0002t0003g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.188-16491T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781180 | |||||||
chr11:77781243 | C | T | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-16554G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781243 | |||||||
chr11:77781371 | T | C | 2 | a0001c0001t0002g0113 a0001c0001t0040g0116 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.188-16682A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781371 | |||||||
chr11:77781536 | T | C | 1 | a0001c0001t0038g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.188-16847A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781536 | |||||||
chr11:77781548 | A | G | 43 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.188-16859T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781548 | |||||||
chr11:77781689 | A | T | 1 | a0001c0001t0002g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.188-17000T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781689 | |||||||
chr11:77781789 | T | G | 1 | a0001c0001t0004g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.188-17100A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781789 | |||||||
chr11:77781895 | C | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-17206G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781895 | |||||||
chr11:77781896 | A | G | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.188-17207T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781896 | |||||||
chr11:77782060 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-17371A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782060 | |||||||
chr11:77782171 | TAATTAC | T | 4 | a0002c0004t0002g0231 a0002c0004t0002g0233 a0002c0004t0002g0234 others(1): Show |
4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-17488_188-1748 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782171 | |||||||
chr11:77782208 | T | C | 1 | a0001c0001t0004g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.188-17519A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782208 | |||||||
chr11:77782257 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG01884.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.188-17568C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782257 | |||||||
chr11:77782307 | G | T | 2 | a0001c0002t0010g0013 a0001c0002t0033g0012 |
2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.188-17618C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782307 | |||||||
chr11:77782412 | G | A | 1 | a0002c0003t0002g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.188-17723C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782412 | |||||||
chr11:77782473 | G | A | 1 | a0002c0003t0002g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-17784C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782473 | |||||||
chr11:77782538 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-17849G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782538 | |||||||
chr11:77782540 | C | CA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(5): Show |
8 | HG01070.hp2 HG01168.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-17852dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782540 | |||||||
chr11:77782958 | T | C | 22 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-18269A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782958 | |||||||
chr11:77782960 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18271G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782960 | |||||||
chr11:77783091 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-18402A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783091 | |||||||
chr11:77783287 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18598C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783287 | |||||||
chr11:77783474 | C | T | 1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.188-18785G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783474 | |||||||
chr11:77783493 | T | C | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-18804A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783493 | |||||||
chr11:77783564 | G | A | 1 | a0001c0001t0023g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-18875C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783564 | |||||||
chr11:77783617 | G | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-18928C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783617 | |||||||
chr11:77783663 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18974C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783663 | |||||||
chr11:77783708 | G | A | 39 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0207 others(36): Show |
39 | HG00140.hp1 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.188-19019C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783708 | |||||||
chr11:77783809 | T | A | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188-19120A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783809 | |||||||
chr11:77783811 | C | T | 1 | a0002c0003t0002g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.188-19122G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783811 | |||||||
chr11:77783833 | C | A | 1 | a0002c0003t0002g0214 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.188-19144G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783833 | |||||||
chr11:77783863 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-19174C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783863 | |||||||
chr11:77784022 | T | A | 1 | a0002c0004t0002g0224 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.188-19333A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784022 | |||||||
chr11:77784102 | G | C | 73 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(70): Show |
73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.188-19413C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784102 | |||||||
chr11:77784110 | C | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-19421G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784110 | |||||||
chr11:77784206 | T | A | 1 | a0001c0002t0003g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.188-19517A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784206 | |||||||
chr11:77784427 | T | C | 1 | a0002c0003t0002g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.188-19738A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784427 | |||||||
chr11:77784599 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-19910G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784599 | |||||||
chr11:77784680 | G | A | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.188-19991C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784680 | |||||||
chr11:77784850 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-20161T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784850 | |||||||
chr11:77784978 | C | T | 5 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): Show |
5 | HG01884.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-20289G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784978 | |||||||
chr11:77785059 | TTC | T | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-20372_188-2037 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785059 | |||||||
chr11:77785126 | C | T | 52 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(49): Show |
52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-20437G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785126 | |||||||
chr11:77785480 | C | T | 1 | a0001c0001t0008g0270 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.188-20791G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785480 | |||||||
chr11:77785521 | C | T | 69 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-20832G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785521 | |||||||
chr11:77785645 | A | T | 42 | a0002c0003t0002g0099 a0002c0003t0002g0203 a0002c0003t0002g0204 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.188-20956T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785645 | |||||||
chr11:77785718 | G | A | 5 | a0001c0001t0006g0118 a0001c0001t0006g0123 a0001c0001t0006g0125 others(2): Show |
5 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-21029C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785718 | |||||||
chr11:77785754 | GA | G | 86 | a0001c0001t0001g0287 a0001c0001t0001g0292 a0001c0001t0001g0332 others(83): Show |
86 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-21066delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785754 | |||||||
chr11:77785791 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-21102G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785791 | |||||||
chr11:77785874 | C | T | 1 | a0001c0001t0004g0150 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.188-21185G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785874 | |||||||
chr11:77785894 | C | T | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.188-21205G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785894 | |||||||
chr11:77785904 | C | T | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188-21215G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785904 | |||||||
chr11:77785917 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.188-21228A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785917 | |||||||
chr11:77785925 | C | CA | 62 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0277 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.188-21237dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | C | CAA | 75 | a0001c0001t0001g0285 a0001c0001t0001g0300 a0001c0001t0002g0109 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.188-21238_188-2123 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | C | CAAA | 24 | a0001c0001t0002g0108 a0001c0001t0002g0114 a0001c0001t0002g0120 others(21): Show |
24 | HG00609.hp1 HG01175.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-21239_188-2123 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | C | CAAAA | 17 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0302 others(14): Show |
17 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-21240_188-2123 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | C | CAAAAA | 7 | a0001c0001t0001g0305 a0001c0001t0004g0135 a0001c0001t0005g0304 others(4): Show |
7 | HG00423.hp1 HG02027.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-21241_188-2123 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | CAAAA | C | 8 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0019 others(5): Show |
8 | HG01081.hp1 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-21240_188-2123 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | CAAAAA | C | 70 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0021 others(67): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.188-21241_188-2123 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785925 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.188-21250_188-2123 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | |||||||
chr11:77785957 | A | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-21268T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785957 | |||||||
chr11:77785992 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-21303C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785992 | |||||||
chr11:77786024 | C | T | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-21335G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786024 | |||||||
chr11:77786073 | T | C | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-21384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786073 | |||||||
chr11:77786349 | C | G | 236 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.188-21660G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786349 | |||||||
chr11:77786701 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-22012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786701 | |||||||
chr11:77786828 | A | T | 2 | a0001c0002t0003g0033 a0001c0002t0003g0047 |
2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.188-22139T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786828 | |||||||
chr11:77786841 | C | T | 1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-22152G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786841 | |||||||
chr11:77786887 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-22198C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786887 | |||||||
chr11:77787006 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-22317C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787006 | |||||||
chr11:77787014 | G | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-22325C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787014 | |||||||
chr11:77787118 | G | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-22429C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787118 | |||||||
chr11:77787195 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-22506G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787195 | |||||||
chr11:77787228 | C | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-22539G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787228 | |||||||
chr11:77787440 | T | C | 73 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.188-22751A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787440 | |||||||
chr11:77787489 | G | A | 1 | a0001c0002t0003g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.188-22800C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787489 | |||||||
chr11:77787521 | T | G | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-22832A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787521 | |||||||
chr11:77787562 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-22873G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787562 | |||||||
chr11:77787569 | T | C | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-22880A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787569 | |||||||
chr11:77787628 | A | T | 1 | a0001c0002t0003g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-22939T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787628 | |||||||
chr11:77787722 | T | C | 236 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.188-23033A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787722 | |||||||
chr11:77787833 | T | TA | 8 | a0001c0001t0001g0095 a0001c0001t0001g0344 a0001c0001t0004g0183 others(5): Show |
8 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-23145dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | |||||||
chr11:77787833 | T | TAAAAAAA others(3): Show |
61 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.188-23154_188-2314 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | |||||||
chr11:77787833 | T | TAAAAAAA others(4): Show |
14 | a0001c0002t0003g0020 a0001c0002t0003g0040 a0001c0002t0003g0052 others(11): Show |
14 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-23155_188-2314 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | |||||||
chr11:77787833 | T | TAAAAAAA others(5): Show |
1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-23156_188-2314 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | |||||||
chr11:77787833 | T | TAAAAAAA others(9): Show |
1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-23145_188-2314 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | |||||||
chr11:77787856 | G | A | 10 | a0002c0003t0002g0099 a0002c0003t0002g0216 a0002c0003t0002g0217 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-23167C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787856 | |||||||
chr11:77787881 | G | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-23192C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787881 | |||||||
chr11:77787887 | T | C | 13 | a0001c0002t0003g0033 a0001c0002t0003g0035 a0001c0002t0003g0036 others(10): Show |
13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-23198A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787887 | |||||||
chr11:77787897 | A | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-23208T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787897 | |||||||
chr11:77787932 | G | A | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.188-23243C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787932 | |||||||
chr11:77788035 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-23346C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788035 | |||||||
chr11:77788142 | C | CA | 35 | a0001c0001t0001g0097 a0001c0001t0001g0264 a0001c0001t0001g0276 others(32): Show |
35 | HG00558.hp1 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.188-23454dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAA | 36 | a0001c0001t0001g0088 a0001c0001t0001g0277 a0001c0001t0001g0280 others(33): Show |
36 | HG00544.hp2 HG00639.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.188-23455_188-2345 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAA | 37 | a0001c0001t0001g0285 a0001c0001t0001g0305 a0001c0001t0002g0108 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.188-23456_188-2345 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAAA | 51 | a0001c0001t0001g0299 a0001c0001t0002g0110 a0001c0001t0002g0124 others(48): Show |
51 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.188-23457_188-2345 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAAAA | 24 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0001t0004g0139 others(21): Show |
24 | HG00099.hp1 HG00597.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.188-23458_188-2345 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAAAAA | 9 | a0001c0001t0004g0136 a0001c0001t0004g0186 a0001c0001t0004g0194 others(6): Show |
9 | HG00741.hp1 HG01256.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-23459_188-2345 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0004g0192 a0001c0001t0042g0174 |
2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.188-23463_188-2345 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.188-23469_188-2345 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CA | C | 25 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0313 others(22): Show |
25 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.188-23454delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CAA | C | 49 | a0001c0001t0001g0290 a0001c0002t0003g0018 a0001c0002t0003g0019 others(46): Show |
49 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.188-23455_188-2345 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0004g0246 a0011c0018t0032g0014 |
2 | HG04115.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.188-23465_188-2345 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0004 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.188-23467_188-2345 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0002g0003 a0001c0002t0010g0013 a0001c0002t0014g0011 others(2): Show |
5 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-23468_188-2345 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788142 | CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(2): Show |
5 | HG01884.hp1 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-23469_188-2345 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | |||||||
chr11:77788185 | T | TA | 53 | a0001c0001t0001g0320 a0001c0001t0005g0038 a0001c0002t0003g0018 others(50): Show |
53 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.188-23497dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788185 | |||||||
chr11:77788217 | G | A | 7 | a0002c0003t0002g0203 a0002c0003t0002g0230 a0002c0003t0002g0239 others(4): Show |
7 | HG00673.hp2 HG02015.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-23528C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788217 | |||||||
chr11:77788341 | C | T | 69 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-23652G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788341 | |||||||
chr11:77788488 | A | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-23799T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788488 | |||||||
chr11:77788497 | TA | T | 109 | a0001c0001t0001g0090 a0001c0001t0001g0290 a0001c0001t0002g0108 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.188-23809delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788497 | |||||||
chr11:77788497 | TAA | T | 123 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0004g0175 others(120): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.188-23810_188-2380 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788497 | |||||||
chr11:77788499 | A | T | 1 | a0001c0001t0004g0152 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188-23810T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788499 | |||||||
chr11:77788515 | G | A | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.188-23826C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788515 | |||||||
chr11:77788533 | T | G | 1 | a0001c0002t0017g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-23844A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788533 | |||||||
chr11:77788541 | T | C | 1 | a0001c0001t0004g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-23852A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788541 | |||||||
chr11:77788632 | G | C | 1 | a0001c0002t0017g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-23943C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788632 | |||||||
chr11:77788632 | G | T | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188-23943C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788632 | |||||||
chr11:77788861 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-24172T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788861 | |||||||
chr11:77789183 | A | G | 1 | a0001c0001t0007g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.188-24494T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789183 | |||||||
chr11:77789316 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0342 |
2 | NA18973.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.188-24627A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789316 | |||||||
chr11:77789405 | G | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-24716C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789405 | |||||||
chr11:77789439 | C | T | 1 | a0001c0001t0041g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.188-24750G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789439 | |||||||
chr11:77789457 | G | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-24768C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789457 | |||||||
chr11:77789544 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-24855G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789544 | |||||||
chr11:77789568 | G | T | 1 | a0001c0001t0002g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.188-24879C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789568 | |||||||
chr11:77789586 | C | T | 3 | a0001c0001t0004g0191 a0001c0002t0003g0041 a0001c0002t0003g0042 |
3 | HG02886.hp2 HG03041.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.188-24897G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789586 | |||||||
chr11:77789596 | C | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-24907G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789596 | |||||||
chr11:77789647 | T | C | 2 | a0001c0001t0001g0095 a0001c0017t0001g0094 |
2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.188-24958A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789647 | |||||||
chr11:77789690 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-25001G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789690 | |||||||
chr11:77789719 | A | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188-25030T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789719 | |||||||
chr11:77790057 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-25368T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790057 | |||||||
chr11:77790216 | T | C | 80 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-25527A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790216 | |||||||
chr11:77790230 | G | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-25541C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790230 | |||||||
chr11:77790376 | C | T | 1 | a0001c0001t0004g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-25687G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790376 | |||||||
chr11:77790402 | T | A | 69 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-25713A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790402 | |||||||
chr11:77790502 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-25813A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790502 | |||||||
chr11:77790619 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.188-25930T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790619 | |||||||
chr11:77790937 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-26248T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790937 | |||||||
chr11:77791017 | C | T | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-26328G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791017 | |||||||
chr11:77791086 | C | T | 80 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(77): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-26397G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791086 | |||||||
chr11:77791124 | C | G | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.188-26435G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791124 | |||||||
chr11:77791303 | T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-26614A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791303 | |||||||
chr11:77791424 | C | G | 52 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(49): Show |
52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-26735G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791424 | |||||||
chr11:77791473 | A | C | 78 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(75): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.188-26784T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791473 | |||||||
chr11:77791473 | A | T | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-26784T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791473 | |||||||
chr11:77791498 | A | C | 2 | a0001c0001t0009g0242 a0001c0001t0009g0245 |
2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.188-26809T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791498 | |||||||
chr11:77791586 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-26897A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791586 | |||||||
chr11:77791634 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-26945G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791634 | |||||||
chr11:77791905 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0289 |
2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.188-27216G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791905 | |||||||
chr11:77791971 | C | T | 7 | a0001c0001t0006g0118 a0001c0001t0006g0121 a0001c0001t0006g0122 others(4): Show |
7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-27282G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791971 | |||||||
chr11:77792166 | G | C | 8 | a0001c0001t0001g0285 a0001c0001t0001g0298 a0001c0001t0001g0299 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-27477C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792166 | |||||||
chr11:77792256 | C | G | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-27567G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792256 | |||||||
chr11:77792367 | C | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-27678G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792367 | |||||||
chr11:77792429 | G | A | 19 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(16): Show |
19 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-27740C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792429 | |||||||
chr11:77792547 | C | G | 1 | a0002c0004t0002g0231 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188-27858G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792547 | |||||||
chr11:77792616 | G | T | 1 | a0001c0002t0035g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.187+27912C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792616 | |||||||
chr11:77792672 | A | G | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+27856T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792672 | |||||||
chr11:77792707 | G | A | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+27821C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792707 | |||||||
chr11:77792749 | A | C | 1 | a0003c0005t0020g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.187+27779T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792749 | |||||||
chr11:77792752 | C | A | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0120 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+27776G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792752 | |||||||
chr11:77792753 | T | A | 12 | a0001c0002t0003g0033 a0001c0002t0003g0041 a0001c0002t0003g0042 others(9): Show |
12 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+27775A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792753 | |||||||
chr11:77792840 | C | T | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+27688G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792840 | |||||||
chr11:77792906 | C | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+27622G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792906 | |||||||
chr11:77792914 | C | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+27614G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792914 | |||||||
chr11:77793058 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+27470C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793058 | |||||||
chr11:77793239 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.187+27289T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793239 | |||||||
chr11:77793328 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+27200T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793328 | |||||||
chr11:77793447 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+27081C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793447 | |||||||
chr11:77793491 | A | C | 1 | a0001c0002t0003g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.187+27037T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793491 | |||||||
chr11:77793663 | C | T | 60 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(57): Show |
60 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.187+26865G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793663 | |||||||
chr11:77793685 | C | T | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.187+26843G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793685 | |||||||
chr11:77793816 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+26712C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793816 | |||||||
chr11:77793950 | T | C | 22 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+26578A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793950 | |||||||
chr11:77793995 | A | T | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+26533T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793995 | |||||||
chr11:77794041 | A | G | 1 | a0001c0001t0004g0148 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.187+26487T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794041 | |||||||
chr11:77794052 | T | C | 1 | a0001c0002t0035g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.187+26476A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794052 | |||||||
chr11:77794172 | T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+26356A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794172 | |||||||
chr11:77794310 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.187+26218G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794310 | |||||||
chr11:77794433 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+26095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794433 | |||||||
chr11:77794491 | C | T | 2 | a0001c0001t0001g0097 a0003c0016t0045g0201 |
2 | HG01261.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+26037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794491 | |||||||
chr11:77794553 | A | C | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.187+25975T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794553 | |||||||
chr11:77794897 | AAAG | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+25628_187+2563 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794897 | |||||||
chr11:77794914 | T | G | 1 | a0001c0002t0031g0075 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.187+25614A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794914 | |||||||
chr11:77794926 | C | T | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187+25602G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794926 | |||||||
chr11:77794998 | C | T | 79 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+25530G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794998 | |||||||
chr11:77795423 | A | T | 1 | a0002c0003t0002g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.187+25105T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795423 | |||||||
chr11:77795453 | C | T | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+25075G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795453 | |||||||
chr11:77795489 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+25039G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795489 | |||||||
chr11:77795649 | T | A | 237 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+24879A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795649 | |||||||
chr11:77795662 | A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+24866T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795662 | |||||||
chr11:77795892 | A | C | 14 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0302 others(11): Show |
14 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.187+24636T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795892 | |||||||
chr11:77795943 | G | A | 1 | a0001c0001t0008g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+24585C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795943 | |||||||
chr11:77796152 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+24376C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796152 | |||||||
chr11:77796165 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+24363G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796165 | |||||||
chr11:77796286 | G | C | 124 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(121): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.187+24242C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796286 | |||||||
chr11:77796374 | G | T | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+24154C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796374 | |||||||
chr11:77796399 | A | G | 5 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(2): Show |
5 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+24129T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796399 | |||||||
chr11:77796495 | T | G | 2 | a0002c0003t0002g0219 a0002c0003t0008g0266 |
2 | HG01515.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.187+24033A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796495 | |||||||
chr11:77796504 | A | C | 1 | a0001c0001t0051g0182 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.187+24024T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796504 | |||||||
chr11:77796864 | AACAG | A | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.187+23660_187+2366 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796864 | |||||||
chr11:77796892 | G | GTGAACTC others(16): Show |
1 | a0001c0001t0005g0254 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.187+23613_187+2363 others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796892 | |||||||
chr11:77797083 | C | T | 1 | a0001c0001t0005g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.187+23445G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797083 | |||||||
chr11:77797108 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+23420G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797108 | |||||||
chr11:77797167 | C | T | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+23361G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797167 | |||||||
chr11:77797510 | C | T | 1 | a0001c0002t0017g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.187+23018G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797510 | |||||||
chr11:77797546 | G | A | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+22982C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797546 | |||||||
chr11:77797773 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.187+22755C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797773 | |||||||
chr11:77797800 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+22728A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797800 | |||||||
chr11:77797833 | CAA | C | 68 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.187+22693_187+2269 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797833 | |||||||
chr11:77797853 | T | C | 1 | a0001c0001t0006g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187+22675A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797853 | |||||||
chr11:77797936 | C | T | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+22592G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797936 | |||||||
chr11:77798307 | G | A | 1 | a0001c0001t0040g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.187+22221C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798307 | |||||||
chr11:77798364 | C | G | 1 | a0001c0001t0004g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+22164G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798364 | |||||||
chr11:77798371 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+22157G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798371 | |||||||
chr11:77798440 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.187+22088G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798440 | |||||||
chr11:77798581 | T | TAAAA | 7 | a0001c0001t0001g0098 a0001c0001t0001g0301 a0001c0001t0001g0329 others(4): Show |
7 | HG02132.hp2 HG02965.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+21943_187+2194 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | T | TAAAAAAA others(6): Show |
1 | a0001c0002t0010g0350 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.187+21934_187+2194 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0005g0261 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.187+21933_187+2194 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TA | T | 29 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 others(26): Show |
29 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.187+21946delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAA | T | 45 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(42): Show |
45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.187+21945_187+2194 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAA | T | 28 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0302 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.187+21944_187+2194 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAA | T | 56 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+21943_187+2194 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAA | T | 25 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0124 others(22): Show |
25 | HG00673.hp2 HG01255.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.187+21942_187+2194 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAA | T | 19 | a0001c0001t0002g0113 a0001c0001t0002g0117 a0001c0001t0004g0180 others(16): Show |
19 | HG00639.hp1 HG01168.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+21941_187+2194 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA | T | 10 | a0001c0001t0002g0112 a0001c0001t0002g0119 a0001c0001t0002g0120 others(7): Show |
10 | HG00099.hp2 HG00639.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+21940_187+2194 others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0002g0111 a0001c0001t0002g0129 a0001c0001t0002g0130 others(4): Show |
7 | HG00741.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+21939_187+2194 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(3): Show |
T | 61 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(58): Show |
61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.187+21937_187+2194 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(4): Show |
T | 7 | a0001c0002t0003g0022 a0001c0002t0003g0035 a0001c0002t0003g0061 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+21936_187+2194 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0010g0013 others(1): Show |
4 | HG01074.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+21934_187+2194 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(7): Show |
T | 5 | a0001c0001t0028g0145 a0001c0002t0016g0005 a0001c0002t0016g0008 others(2): Show |
5 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+21933_187+2194 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0003c0016t0045g0201 |
3 | HG03195.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.187+21932_187+2194 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(9): Show |
T | 4 | a0001c0001t0001g0280 a0001c0001t0001g0285 a0003c0005t0020g0199 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+21931_187+2194 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0002g0284 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.187+21930_187+2194 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(12): Show |
T | 5 | a0001c0001t0001g0311 a0001c0001t0004g0135 a0001c0001t0005g0253 others(2): Show |
5 | HG01975.hp2 HG02602.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+21928_187+2194 others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(13): Show |
T | 1 | a0001c0001t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+21927_187+2194 others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798581 | TAAAAAAA others(14): Show |
T | 2 | a0001c0002t0003g0036 a0001c0002t0003g0037 |
2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.187+21926_187+2194 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | |||||||
chr11:77798619 | A | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+21909T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798619 | |||||||
chr11:77798928 | C | T | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187+21600G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798928 | |||||||
chr11:77798964 | TAA | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(75): Show |
78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.187+21562_187+2156 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798964 | |||||||
chr11:77799344 | T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+21184A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799344 | |||||||
chr11:77799501 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+21027G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799501 | |||||||
chr11:77799504 | C | CA | 81 | a0001c0001t0001g0329 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+21023dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799504 | |||||||
chr11:77799561 | A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+20967T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799561 | |||||||
chr11:77799848 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.187+20680A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799848 | |||||||
chr11:77800106 | G | A | 1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187+20422C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800106 | |||||||
chr11:77800198 | A | G | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+20330T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800198 | |||||||
chr11:77800250 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+20278C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800250 | |||||||
chr11:77800337 | C | G | 1 | a0002c0003t0050g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.187+20191G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800337 | |||||||
chr11:77800356 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+20172A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800356 | |||||||
chr11:77800366 | C | T | 1 | a0012c0008t0003g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.187+20162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800366 | |||||||
chr11:77800431 | G | A | 1 | a0003c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+20097C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800431 | |||||||
chr11:77800434 | G | T | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187+20094C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800434 | |||||||
chr11:77800436 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+20092C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800436 | |||||||
chr11:77800742 | C | A | 1 | a0001c0001t0009g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187+19786G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800742 | |||||||
chr11:77800927 | C | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+19601G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800927 | |||||||
chr11:77801012 | CA | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+19515delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801012 | |||||||
chr11:77801139 | T | C | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19389A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801139 | |||||||
chr11:77801321 | G | A | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+19207C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801321 | |||||||
chr11:77801360 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+19168C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801360 | |||||||
chr11:77801377 | G | A | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+19151C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801377 | |||||||
chr11:77801381 | G | A | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19147C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801381 | |||||||
chr11:77801433 | A | G | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19095T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801433 | |||||||
chr11:77801453 | G | A | 1 | a0001c0002t0003g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.187+19075C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801453 | |||||||
chr11:77801573 | G | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.187+18955C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801573 | |||||||
chr11:77801617 | G | A | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.187+18911C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801617 | |||||||
chr11:77801805 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.187+18723G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801805 | |||||||
chr11:77802052 | G | A | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.187+18476C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802052 | |||||||
chr11:77802095 | C | T | 5 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+18433G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802095 | |||||||
chr11:77802179 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.187+18349C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802179 | |||||||
chr11:77802342 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+18186A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802342 | |||||||
chr11:77802427 | G | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+18101C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802427 | |||||||
chr11:77802787 | G | A | 12 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0302 others(9): Show |
12 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+17741C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802787 | |||||||
chr11:77802793 | C | T | 1 | a0001c0001t0055g0144 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.187+17735G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802793 | |||||||
chr11:77802905 | T | C | 1 | a0001c0002t0003g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.187+17623A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802905 | |||||||
chr11:77803170 | G | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+17358C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803170 | |||||||
chr11:77803311 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+17217G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803311 | |||||||
chr11:77803384 | C | T | 3 | a0001c0002t0010g0013 a0001c0002t0033g0012 a0011c0018t0032g0014 |
3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.187+17144G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803384 | |||||||
chr11:77803385 | G | A | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+17143C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803385 | |||||||
chr11:77803388 | T | G | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+17140A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803388 | |||||||
chr11:77803458 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+17070G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803458 | |||||||
chr11:77803460 | A | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+17068T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803460 | |||||||
chr11:77803606 | C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+16922G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803606 | |||||||
chr11:77803713 | G | C | 1 | a0001c0001t0002g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.187+16815C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803713 | |||||||
chr11:77804184 | T | C | 113 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(110): Show |
113 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.187+16344A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804184 | |||||||
chr11:77804286 | G | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+16242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804286 | |||||||
chr11:77804325 | G | A | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.187+16203C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804325 | |||||||
chr11:77804590 | A | T | 3 | a0001c0001t0022g0140 a0001c0001t0022g0141 a0001c0001t0054g0142 |
3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+15938T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804590 | |||||||
chr11:77804683 | A | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+15845T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804683 | |||||||
chr11:77804916 | A | C | 2 | a0001c0002t0016g0005 a0001c0002t0016g0008 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.187+15612T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804916 | |||||||
chr11:77805190 | G | C | 72 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+15338C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805190 | |||||||
chr11:77805217 | C | T | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.187+15311G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805217 | |||||||
chr11:77805442 | A | G | 17 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0110 others(14): Show |
17 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+15086T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805442 | |||||||
chr11:77805625 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.187+14903T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805625 | |||||||
chr11:77805726 | G | A | 2 | a0001c0001t0008g0269 a0001c0001t0008g0270 |
2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.187+14802C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805726 | |||||||
chr11:77805727 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+14801A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805727 | |||||||
chr11:77806341 | G | A | 1 | a0008c0011t0007g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.187+14187C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806341 | |||||||
chr11:77806345 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.187+14183A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806345 | |||||||
chr11:77806372 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+14156C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806372 | |||||||
chr11:77806467 | T | C | 1 | a0001c0001t0004g0191 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.187+14061A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806467 | |||||||
chr11:77806474 | A | T | 22 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+14054T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806474 | |||||||
chr11:77806493 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.187+14035A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806493 | |||||||
chr11:77806699 | G | C | 113 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(110): Show |
113 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.187+13829C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806699 | |||||||
chr11:77806766 | C | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+13762G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806766 | |||||||
chr11:77806798 | A | G | 1 | a0001c0001t0004g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.187+13730T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806798 | |||||||
chr11:77806927 | T | G | 43 | a0001c0002t0003g0018 a0001c0002t0003g0022 a0001c0002t0003g0023 others(40): Show |
43 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.187+13601A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806927 | |||||||
chr11:77806952 | T | C | 3 | a0002c0003t0002g0204 a0002c0003t0002g0205 a0002c0003t0002g0206 |
3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+13576A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806952 | |||||||
chr11:77807209 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+13319A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807209 | |||||||
chr11:77807572 | G | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+12956C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807572 | |||||||
chr11:77807582 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.187+12946A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807582 | |||||||
chr11:77807616 | CATAAAT | C | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+12906_187+1291 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807616 | |||||||
chr11:77807634 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12894T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807634 | |||||||
chr11:77807663 | G | T | 3 | a0001c0001t0022g0140 a0001c0001t0022g0141 a0001c0001t0054g0142 |
3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+12865C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807663 | |||||||
chr11:77807764 | G | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12764C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807764 | |||||||
chr11:77807787 | G | C | 89 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(86): Show |
89 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.187+12741C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807787 | |||||||
chr11:77807823 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+12705C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807823 | |||||||
chr11:77807963 | G | C | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.187+12565C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807963 | |||||||
chr11:77808031 | A | T | 22 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(19): Show |
22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+12497T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808031 | |||||||
chr11:77808353 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12175T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808353 | |||||||
chr11:77808355 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12173T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808355 | |||||||
chr11:77808356 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12172G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808356 | |||||||
chr11:77808413 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+12115G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808413 | |||||||
chr11:77808463 | C | T | 2 | a0002c0003t0021g0209 a0002c0003t0021g0210 |
2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.187+12065G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808463 | |||||||
chr11:77808469 | G | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12059C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808469 | |||||||
chr11:77808513 | TTCAAATA others(312): Show |
T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+11696_187+1201 others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808513 | |||||||
chr11:77808527 | C | CT | 41 | a0001c0001t0004g0136 a0001c0001t0004g0196 a0001c0001t0004g0197 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.187+12000dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | |||||||
chr11:77808527 | C | CTT | 127 | a0001c0001t0001g0264 a0001c0001t0001g0290 a0001c0001t0001g0308 others(124): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.187+11999_187+1200 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | |||||||
chr11:77808527 | C | CTTT | 77 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0088 others(74): Show |
77 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.187+11998_187+1200 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | |||||||
chr11:77808527 | C | CTTTT | 17 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0095 others(14): Show |
17 | HG00408.hp1 HG00609.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+11997_187+1200 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | |||||||
chr11:77808565 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187+11963C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808565 | |||||||
chr11:77808626 | C | T | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+11902G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808626 | |||||||
chr11:77808908 | G | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.187+11620C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808908 | |||||||
chr11:77809020 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 |
3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+11508G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809020 | |||||||
chr11:77809086 | A | G | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+11442T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809086 | |||||||
chr11:77809165 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+11363A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809165 | |||||||
chr11:77809327 | T | C | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+11201A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809327 | |||||||
chr11:77809410 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+11118C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809410 | |||||||
chr11:77809827 | T | A | 1 | a0011c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.187+10701A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809827 | |||||||
chr11:77810344 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+10184T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810344 | |||||||
chr11:77810358 | A | G | 4 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+10170T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810358 | |||||||
chr11:77810400 | C | T | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.187+10128G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810400 | |||||||
chr11:77810494 | C | A | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.187+10034G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810494 | |||||||
chr11:77810495 | C | G | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.187+10033G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810495 | |||||||
chr11:77810570 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.187+9958C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810570 | |||||||
chr11:77810682 | T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+9846A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810682 | |||||||
chr11:77811079 | T | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+9449A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811079 | |||||||
chr11:77811142 | A | T | 237 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0108 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+9386T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811142 | |||||||
chr11:77811144 | T | C | 1 | a0001c0001t0007g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.187+9384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811144 | |||||||
chr11:77811173 | G | A | 1 | a0002c0003t0002g0348 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.187+9355C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811173 | |||||||
chr11:77811188 | C | T | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+9340G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811188 | |||||||
chr11:77811338 | A | G | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0051g0182 |
3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.187+9190T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811338 | |||||||
chr11:77811587 | G | A | 113 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(110): Show |
113 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.187+8941C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811587 | |||||||
chr11:77811631 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8897G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811631 | |||||||
chr11:77811750 | A | G | 4 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0312 others(1): Show |
4 | HG00558.hp1 NA18982.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+8778T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811750 | |||||||
chr11:77811790 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.187+8738C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811790 | |||||||
chr11:77811931 | G | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8597C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811931 | |||||||
chr11:77812038 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8490A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812038 | |||||||
chr11:77812039 | G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+8489C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812039 | |||||||
chr11:77812149 | A | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+8379T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812149 | |||||||
chr11:77812187 | A | G | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+8341T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812187 | |||||||
chr11:77812270 | T | C | 1 | a0001c0002t0037g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.187+8258A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812270 | |||||||
chr11:77812381 | A | G | 6 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 others(3): Show |
6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+8147T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812381 | |||||||
chr11:77812419 | T | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8109A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812419 | |||||||
chr11:77812438 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8090G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812438 | |||||||
chr11:77812690 | C | A | 2 | a0002c0003t0002g0208 a0002c0003t0002g0227 |
2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.187+7838G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812690 | |||||||
chr11:77812751 | G | A | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+7777C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812751 | |||||||
chr11:77812884 | C | CA | 23 | a0001c0002t0003g0018 a0001c0002t0003g0061 a0001c0002t0003g0062 others(20): Show |
23 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.187+7643dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | |||||||
chr11:77812884 | CA | C | 88 | a0001c0001t0001g0276 a0001c0001t0001g0342 a0001c0001t0002g0004 others(85): Show |
88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+7643delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | |||||||
chr11:77812884 | CAA | C | 107 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(104): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.187+7642_187+7643d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | |||||||
chr11:77812988 | A | G | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.187+7540T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812988 | |||||||
chr11:77812997 | A | G | 1 | a0001c0001t0004g0137 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.187+7531T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812997 | |||||||
chr11:77813305 | T | C | 6 | a0001c0002t0010g0013 a0001c0002t0014g0009 a0001c0002t0014g0011 others(3): Show |
6 | HG01074.hp1 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+7223A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813305 | |||||||
chr11:77813469 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.187+7059G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813469 | |||||||
chr11:77813622 | G | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.187+6906C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813622 | |||||||
chr11:77813676 | T | G | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+6852A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813676 | |||||||
chr11:77813714 | C | T | 6 | a0001c0002t0010g0013 a0001c0002t0014g0009 a0001c0002t0014g0011 others(3): Show |
6 | HG01074.hp1 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+6814G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813714 | |||||||
chr11:77813752 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.187+6776C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813752 | |||||||
chr11:77813808 | A | T | 10 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(7): Show |
10 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+6720T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813808 | |||||||
chr11:77813820 | G | GAC | 78 | a0001c0001t0001g0087 a0001c0001t0001g0279 a0001c0001t0001g0334 others(75): Show |
78 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.187+6706_187+6707d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | G | GACAC | 61 | a0001c0001t0001g0274 a0001c0001t0001g0280 a0001c0001t0001g0282 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.187+6704_187+6707d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | G | GACACAC | 57 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0088 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.187+6702_187+6707d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | G | GACACACA others(1): Show |
7 | a0001c0001t0001g0264 a0001c0001t0001g0276 a0001c0001t0001g0332 others(4): Show |
7 | HG01109.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+6700_187+6707d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | G | GACACACA others(3): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.187+6698_187+6707d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | GAC | G | 6 | a0001c0001t0002g0108 a0001c0001t0004g0135 a0001c0001t0009g0242 others(3): Show |
6 | HG01928.hp2 HG02602.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+6706_187+6707d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | GACACAC | G | 9 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0002t0003g0019 others(6): Show |
9 | HG02523.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+6702_187+6707d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | GACACACA others(1): Show |
G | 72 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0022 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+6700_187+6707d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77813820 | GACACACA others(9): Show |
G | 1 | a0001c0001t0004g0134 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.187+6692_187+6707d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | |||||||
chr11:77814157 | G | A | 114 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(111): Show |
114 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+6371C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814157 | |||||||
chr11:77814208 | A | AAAG | 304 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(301): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.187+6317_187+6319d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814208 | |||||||
chr11:77814263 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+6265G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814263 | |||||||
chr11:77814264 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+6264C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814264 | |||||||
chr11:77814280 | C | T | 1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.187+6248G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814280 | |||||||
chr11:77814356 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6172T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814356 | |||||||
chr11:77814358 | C | G | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+6170G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814358 | |||||||
chr11:77814364 | A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6164T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814364 | |||||||
chr11:77814373 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6155A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814373 | |||||||
chr11:77814375 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6153A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814375 | |||||||
chr11:77814379 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6149A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814379 | |||||||
chr11:77814381 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6147A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814381 | |||||||
chr11:77814382 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6146T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814382 | |||||||
chr11:77814384 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6144A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814384 | |||||||
chr11:77814385 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6143A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814385 | |||||||
chr11:77814386 | C | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6142G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814386 | |||||||
chr11:77814389 | A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6139T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814389 | |||||||
chr11:77814390 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6138G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814390 | |||||||
chr11:77814391 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6137A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814391 | |||||||
chr11:77814395 | C | CGGGGGGG others(3): Show |
1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6132_187+6133i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814395 | |||||||
chr11:77814399 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6129T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814399 | |||||||
chr11:77814402 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6126A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814402 | |||||||
chr11:77814403 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6125A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814403 | |||||||
chr11:77814412 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6116T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814412 | |||||||
chr11:77814419 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6109G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814419 | |||||||
chr11:77814420 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6108A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814420 | |||||||
chr11:77814421 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6107A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814421 | |||||||
chr11:77814423 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6105T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814423 | |||||||
chr11:77814425 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6103G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814425 | |||||||
chr11:77814426 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6102G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814426 | |||||||
chr11:77814427 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6101G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814427 | |||||||
chr11:77814428 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6100T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814428 | |||||||
chr11:77814431 | A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6097T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814431 | |||||||
chr11:77814432 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6096T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814432 | |||||||
chr11:77814433 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6095A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814433 | |||||||
chr11:77814434 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6094A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814434 | |||||||
chr11:77814435 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6093G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814435 | |||||||
chr11:77814436 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6092T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814436 | |||||||
chr11:77814437 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6091T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814437 | |||||||
chr11:77814440 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6088G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814440 | |||||||
chr11:77814441 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6087G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814441 | |||||||
chr11:77814442 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6086G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814442 | |||||||
chr11:77814443 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6085A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814443 | |||||||
chr11:77814444 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6084T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814444 | |||||||
chr11:77814445 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6083T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814445 | |||||||
chr11:77814446 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6082G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814446 | |||||||
chr11:77814447 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6081A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814447 | |||||||
chr11:77814448 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6080G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814448 | |||||||
chr11:77814449 | T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6079A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814449 | |||||||
chr11:77814457 | A | G | 3 | a0003c0005t0020g0199 a0003c0005t0020g0200 a0003c0016t0045g0201 |
3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+6071T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814457 | |||||||
chr11:77814471 | AGTCTCGC others(4): Show |
A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6046_187+6056d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814471 | |||||||
chr11:77814476 | C | A | 1 | a0001c0001t0004g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.187+6052G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814476 | |||||||
chr11:77814510 | A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6018T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814510 | |||||||
chr11:77814515 | G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6013C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814515 | |||||||
chr11:77814516 | G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6012C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814516 | |||||||
chr11:77814525 | A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6003T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814525 | |||||||
chr11:77814538 | C | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5990G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814538 | |||||||
chr11:77814539 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5989T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814539 | |||||||
chr11:77814542 | T | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5986A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814542 | |||||||
chr11:77814549 | G | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5979C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814549 | |||||||
chr11:77814563 | G | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5965C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814563 | |||||||
chr11:77814579 | G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5949C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814579 | |||||||
chr11:77814583 | T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5945A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814583 | |||||||
chr11:77814595 | G | A | 9 | a0001c0001t0001g0274 a0001c0001t0001g0334 a0001c0001t0001g0335 others(6): Show |
9 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+5933C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814595 | |||||||
chr11:77814602 | G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5926C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814602 | |||||||
chr11:77814604 | T | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5924A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814604 | |||||||
chr11:77814606 | T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5922A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814606 | |||||||
chr11:77814608 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0005g0038 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+5920T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814608 | |||||||
chr11:77814609 | C | A | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+5919G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814609 | |||||||
chr11:77814618 | G | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5910C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814618 | |||||||
chr11:77814619 | T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5909A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814619 | |||||||
chr11:77814626 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5902T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814626 | |||||||
chr11:77814644 | C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5884G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814644 | |||||||
chr11:77814646 | A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5882T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814646 | |||||||
chr11:77814661 | G | C | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+5867C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814661 | |||||||
chr11:77814666 | A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5862T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814666 | |||||||
chr11:77814689 | G | A | 1 | a0001c0002t0003g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.187+5839C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814689 | |||||||
chr11:77814692 | G | A | 72 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0130 others(69): Show |
72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+5836C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814692 | |||||||
chr11:77814699 | C | A | 1 | a0003c0016t0045g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.187+5829G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814699 | |||||||
chr11:77814881 | C | A | 1 | a0001c0001t0001g0342 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.187+5647G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814881 | |||||||
chr11:77814890 | G | GT | 70 | a0001c0001t0001g0276 a0001c0001t0005g0038 a0001c0001t0023g0275 others(67): Show |
70 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.187+5637dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814890 | |||||||
chr11:77814890 | G | T | 17 | a0001c0001t0005g0252 a0001c0001t0005g0253 a0001c0001t0005g0254 others(14): Show |
17 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+5638C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814890 | |||||||
chr11:77815016 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.187+5512T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815016 | |||||||
chr11:77815121 | T | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+5407A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815121 | |||||||
chr11:77815158 | T | A | 6 | a0001c0002t0003g0019 a0001c0002t0003g0020 a0001c0002t0003g0021 others(3): Show |
6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+5370A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815158 | |||||||
chr11:77815179 | C | T | 1 | a0001c0001t0052g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.187+5349G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815179 | |||||||
chr11:77815389 | C | A | 1 | a0001c0002t0030g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.187+5139G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815389 | |||||||
chr11:77815428 | C | A | 89 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(86): Show |
89 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.187+5100G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815428 | |||||||
chr11:77815490 | A | C | 1 | a0001c0001t0004g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.187+5038T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815490 | |||||||
chr11:77815538 | T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+4990A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815538 | |||||||
chr11:77815616 | T | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.187+4912A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815616 | |||||||
chr11:77815748 | A | T | 78 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.187+4780T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815748 | |||||||
chr11:77815760 | CCCA | C | 81 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+4765_187+4767d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815760 | |||||||
chr11:77815769 | T | G | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4759A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815769 | |||||||
chr11:77815857 | C | T | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.187+4671G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815857 | |||||||
chr11:77815993 | C | T | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4535G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815993 | |||||||
chr11:77816687 | C | T | 13 | a0001c0001t0001g0264 a0001c0001t0005g0252 a0001c0001t0005g0253 others(10): Show |
13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+3841G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816687 | |||||||
chr11:77816909 | A | C | 6 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(3): Show |
6 | HG01243.hp2 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3619T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816909 | |||||||
chr11:77816986 | T | C | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.187+3542A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816986 | |||||||
chr11:77817077 | A | G | 3 | a0001c0002t0014g0009 a0001c0002t0014g0011 a0001c0002t0034g0010 |
3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.187+3451T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817077 | |||||||
chr11:77817115 | C | G | 280 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(277): Show |
280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.187+3413G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817115 | |||||||
chr11:77817293 | T | C | 82 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+3235A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817293 | |||||||
chr11:77817741 | A | G | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+2787T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817741 | |||||||
chr11:77817804 | A | T | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.187+2724T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817804 | |||||||
chr11:77817882 | T | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+2646A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817882 | |||||||
chr11:77818062 | C | T | 2 | a0001c0001t0004g0105 a0001c0001t0004g0106 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.187+2466G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818062 | |||||||
chr11:77818071 | G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+2457C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818071 | |||||||
chr11:77818180 | G | C | 2 | a0002c0003t0002g0240 a0002c0003t0002g0241 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.187+2348C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818180 | |||||||
chr11:77818393 | A | G | 4 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0103 others(1): Show |
4 | HG02083.hp2 NA18612.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+2135T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818393 | |||||||
chr11:77818482 | C | T | 307 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(304): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.187+2046G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818482 | |||||||
chr11:77818631 | T | C | 1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.187+1897A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818631 | |||||||
chr11:77818650 | A | G | 1 | a0001c0001t0023g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.187+1878T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818650 | |||||||
chr11:77818919 | A | C | 4 | a0001c0002t0016g0005 a0001c0002t0016g0008 a0001c0002t0017g0006 others(1): Show |
4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1609T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818919 | |||||||
chr11:77819001 | T | G | 4 | a0001c0001t0009g0242 a0001c0001t0009g0243 a0001c0001t0009g0244 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1527A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819001 | |||||||
chr11:77819092 | G | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.187+1436C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819092 | |||||||
chr11:77819249 | C | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+1279G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819249 | |||||||
chr11:77819256 | G | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.187+1272C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819256 | |||||||
chr11:77819409 | G | C | 1 | a0005c0007t0001g0349 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.187+1119C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819409 | |||||||
chr11:77819524 | A | C | 4 | a0001c0002t0003g0018 a0001c0002t0003g0019 a0001c0002t0003g0020 others(1): Show |
4 | HG02132.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1004T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819524 | |||||||
chr11:77819814 | T | C | 1 | a0001c0001t0041g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.187+714A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819814 | |||||||
chr11:77819820 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.187+708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819820 | |||||||
chr11:77819825 | C | A | 83 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+703G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819825 | |||||||
chr11:77819907 | T | C | 83 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+621A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819907 | |||||||
chr11:77819953 | A | C | 1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.187+575T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819953 | |||||||
chr11:77819997 | G | C | 68 | a0001c0001t0005g0038 a0001c0002t0003g0018 a0001c0002t0003g0019 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+531C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819997 | |||||||
chr11:77820008 | C | G | 1 | a0002c0003t0002g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.187+520G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820008 | |||||||
chr11:77820010 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.187+518C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820010 | |||||||
chr11:77820112 | G | A | 2 | a0001c0002t0010g0350 a0001c0002t0010g0351 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+416C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820112 | |||||||
chr11:77820235 | G | C | 116 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(113): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.187+293C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820235 | |||||||
chr11:77820269 | T | G | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.187+259A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820269 | |||||||
chr11:77820297 | C | T | 12 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+231G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820297 | |||||||
chr11:77820480 | C | G | 83 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+48G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820480 |