Item | Value |
---|---|
geneid | 96459 |
ensemblid | ENSG00000217128.13 |
hgncid | 29418 |
symbol | FNIP1 |
name | folliculin interacting protein 1 |
refseq_nuc | NM_133372.3 |
refseq_prot | NP_588613.3 |
ensembl_nuc | ENST00000510461.6 |
ensembl_prot | ENSP00000421985.1 |
mane_status | MANE Select |
chr | chr5 |
start | 131641714 |
end | 131797017 |
strand | - |
ver | v1.2 |
region | chr5:131641714-131797017 |
region5000 | chr5:131636714-131802017 |
regionname0 | FNIP1_chr5_131641714_131797017 |
regionname5000 | FNIP1_chr5_131636714_131802017 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1166 | 253 | 67 | 53 | 116 | 3 | 14 | 101 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0002 | 1/0 | 1166 | 54 | 6 | 11 | 27 | 1 | 8 | 21 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0003 | 0/0 | 1166 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0004 | 0/0 | 1166 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0005 | 0/0 | 1166 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0006 | 0/0 | 1166 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0007 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0008 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0009 | 0/0 | 1166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
a0010 | 0/1 | 1166 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | MAPTL others(1161): Show |
chr5 | 131636714 | 131802017 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3498 | 235 | 58 | 53 | 109 | 3 | 12 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0004 | 0/0 | 3498 | 6 | 0 | 0 | 5 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0005 | 0/0 | 3498 | 6 | 6 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0008 | 0/0 | 3498 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0012 | 0/0 | 3498 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0013 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0014 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0001c0016 | 0/0 | 3498 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0002c0002 | 1/0 | 3498 | 51 | 6 | 8 | 27 | 1 | 8 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0002c0006 | 0/0 | 3498 | 3 | 0 | 3 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0003c0003 | 0/0 | 3498 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0004c0007 | 0/0 | 3498 | 3 | 3 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0005c0009 | 0/0 | 3498 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0006c0010 | 0/0 | 3498 | 2 | 0 | 0 | 0 | 0 | 2 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0007c0017 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0008c0011 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0009c0015 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 | ||
a0010c0018 | 0/1 | 3498 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATGGC others(3493): Show |
chr5 | 131636714 | 131802017 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6567 | 108 | 18 | 28 | 53 | 2 | 7 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0002 | 0/0 | 6568 | 50 | 2 | 10 | 33 | 1 | 4 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0003 | 0/0 | 6567 | 28 | 20 | 8 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0005 | 0/0 | 6569 | 18 | 4 | 5 | 9 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0006 | 0/0 | 6568 | 6 | 0 | 0 | 6 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0007 | 0/0 | 6567 | 7 | 7 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0008 | 0/0 | 6566 | 5 | 4 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6561): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0009 | 0/0 | 6566 | 5 | 0 | 0 | 5 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6561): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0011 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0012 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0013 | 0/0 | 6569 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0016 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0020 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0021 | 0/0 | 6569 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0022 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0001t0023 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0004t0001 | 0/0 | 6567 | 6 | 0 | 0 | 5 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0005t0001 | 0/0 | 6567 | 4 | 4 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0005t0006 | 0/0 | 6568 | 2 | 2 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0008t0002 | 0/0 | 6568 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0001c0012t0001 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0013t0003 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0014t0001 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0001c0016t0001 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0002 | 1/0 | 6568 | 24 | 4 | 8 | 4 | 1 | 6 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0004 | 0/0 | 6568 | 22 | 0 | 0 | 21 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0005 | 0/0 | 6569 | 2 | 1 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0010 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0017 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0002c0002t0018 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6561): Show |
chr5 | 131636714 | 131802017 |
a0002c0006t0004 | 0/0 | 6568 | 2 | 0 | 2 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0002c0006t0010 | 0/0 | 6569 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0003c0003t0002 | 0/0 | 6568 | 10 | 10 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0004c0007t0001 | 0/0 | 6567 | 3 | 3 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0005c0009t0014 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6561): Show |
chr5 | 131636714 | 131802017 |
a0005c0009t0015 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0006c0010t0001 | 0/0 | 6567 | 2 | 0 | 0 | 0 | 0 | 2 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0007c0017t0006 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6563): Show |
chr5 | 131636714 | 131802017 |
a0008c0011t0005 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6564): Show |
chr5 | 131636714 | 131802017 |
a0009c0015t0001 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
a0010c0018t0019 | 0/1 | 6567 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | ATATG others(6562): Show |
chr5 | 131636714 | 131802017 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0013g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0016g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0001t0023g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0005t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0008t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0008t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0012t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0013t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0014t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0001c0016t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0017g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0002t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0006t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0006t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0002c0006t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0003c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0004c0007t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0004c0007t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0004c0007t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0005c0009t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0005c0009t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0006c0010t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0006c0010t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0007c0017t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0008c0011t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0009c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
a0010c0018t0019g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01099 | hp1 | a0001 | c0001 | t0005 | g0277 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0161 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0325 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0283 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0046 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0160 | EUR | IBS | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01884 | hp1 | a0003 | c0003 | t0002 | g0312 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0127 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0146 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01978 | hp1 | a0002 | c0006 | t0010 | g0139 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01981 | hp2 | a0002 | c0006 | t0004 | g0142 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0156 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02056 | hp1 | a0002 | c0002 | t0004 | g0284 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0297 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02071 | hp1 | a0007 | c0017 | t0006 | g0018 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02071 | hp2 | a0002 | c0002 | t0017 | g0285 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0233 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0311 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02280 | hp1 | a0003 | c0003 | t0002 | g0316 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02293 | hp1 | a0002 | c0006 | t0004 | g0126 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PEL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02572 | hp1 | a0001 | c0005 | t0006 | g0066 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0273 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02615 | hp1 | a0005 | c0009 | t0015 | g0052 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02615 | hp2 | a0001 | c0013 | t0003 | g0027 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0324 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02717 | hp1 | a0001 | c0014 | t0001 | g0326 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02723 | hp1 | a0003 | c0003 | t0002 | g0318 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02738 | hp1 | a0001 | c0001 | t0021 | g0012 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0282 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02809 | hp1 | a0001 | c0005 | t0001 | g0067 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0078 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02965 | hp2 | a0003 | c0003 | t0002 | g0320 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0073 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02976 | hp1 | a0004 | c0007 | t0001 | g0183 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03041 | hp1 | a0005 | c0009 | t0014 | g0051 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03098 | hp1 | a0004 | c0007 | t0001 | g0176 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03130 | hp1 | a0004 | c0007 | t0001 | g0184 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03130 | hp2 | a0003 | c0003 | t0002 | g0319 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0068 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0308 | AFR | ESN | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0141 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03225 | hp1 | a0003 | c0003 | t0002 | g0313 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03453 | hp2 | a0003 | c0003 | t0002 | g0317 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0289 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03688 | hp1 | a0006 | c0010 | t0001 | g0292 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03927 | hp1 | a0001 | c0004 | t0001 | g0298 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03927 | hp2 | a0002 | c0002 | t0004 | g0135 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0149 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04199 | hp1 | a0001 | c0012 | t0001 | g0173 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG04199 | hp2 | a0002 | c0002 | t0005 | g0145 | SAS | STU | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18522 | hp2 | a0003 | c0003 | t0002 | g0315 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18939 | hp2 | a0008 | c0011 | t0005 | g0121 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18940 | hp1 | a0001 | c0004 | t0001 | g0062 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18940 | hp2 | a0001 | c0008 | t0002 | g0286 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18941 | hp2 | a0001 | c0001 | t0009 | g0181 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18944 | hp1 | a0002 | c0002 | t0004 | g0138 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18949 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18954 | hp2 | a0002 | c0002 | t0004 | g0137 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18957 | hp2 | a0002 | c0002 | t0004 | g0147 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18959 | hp2 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18962 | hp2 | a0002 | c0002 | t0004 | g0164 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18966 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18970 | hp1 | a0001 | c0001 | t0023 | g0229 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18977 | hp1 | a0009 | c0015 | t0001 | g0192 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18977 | hp2 | a0002 | c0002 | t0010 | g0136 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18978 | hp1 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18978 | hp2 | a0002 | c0002 | t0004 | g0288 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18980 | hp1 | a0002 | c0002 | t0004 | g0132 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18980 | hp2 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18981 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0157 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18991 | hp2 | a0001 | c0004 | t0001 | g0259 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18995 | hp1 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18995 | hp2 | a0001 | c0001 | t0009 | g0217 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19001 | hp2 | a0001 | c0001 | t0006 | g0241 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19005 | hp1 | a0002 | c0002 | t0004 | g0007 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19007 | hp2 | a0001 | c0004 | t0001 | g0250 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19010 | hp2 | a0002 | c0002 | t0004 | g0144 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19012 | hp1 | a0002 | c0002 | t0004 | g0140 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0069 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19058 | hp1 | a0001 | c0001 | t0022 | g0208 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19058 | hp2 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19064 | hp2 | a0001 | c0001 | t0016 | g0103 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19065 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19074 | hp2 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19076 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19077 | hp2 | a0001 | c0008 | t0002 | g0111 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19080 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19240 | hp1 | a0001 | c0005 | t0006 | g0071 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | ASW | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0323 | AFR | ASW | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | TSI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20905 | hp1 | a0006 | c0010 | t0001 | g0205 | SAS | GIH | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | GIH | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01123 | hp1 | a0001 | c0001 | t0013 | g0321 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02486 | hp2 | a0002 | c0002 | t0018 | g0059 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02559 | hp1 | a0003 | c0003 | t0002 | g0314 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG02559 | hp2 | a0001 | c0016 | t0001 | g0063 | AFR | ACB | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0232 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0302 | AFR | USA | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | LWK | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
homoSapiens | chm13v2 | a0010 | c0018 | t0019 | g0014 | REF | REF | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0109 | REF | REF | FNIP1_chr5_131636714_131802017 | FNIP1 | chr5 | 131636714 | 131802017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:131671665 | C | T | 1 | a0009 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2779G>A | p.Val927Ile | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2875/6568 | 2779/3501 | 927/1166 | chr5 | 131671665 | |||
chr5:131671794 | A | G | 1 | a0005 | 2 | HG02615.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.2650T>C | p.Phe884Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2746/6568 | 2650/3501 | 884/1166 | chr5 | 131671794 | |||
chr5:131671914 | T | C | 1 | a0004 | 3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.2530A>G | p.Ile844Val | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2626/6568 | 2530/3501 | 844/1166 | chr5 | 131671914 | |||
chr5:131672232 | C | A | 1 | a0003 | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
missense_variant | MODERATE | c.2212G>T | p.Val738Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2308/6568 | 2212/3501 | 738/1166 | chr5 | 131672232 | |||
chr5:131672501 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
273 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(270): Show |
missense_variant | MODERATE | c.1943A>G | p.Gln648Arg | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2039/6568 | 1943/3501 | 648/1166 | chr5 | 131672501 | |||
chr5:131677804 | T | C | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1418A>G | p.Asn473Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/18 | 1514/6568 | 1418/3501 | 473/1166 | chr5 | 131677804 | |||
chr5:131704262 | T | C | 1 | a0006 | 2 | HG03688.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.919A>G | p.Ile307Val | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/18 | 1015/6568 | 919/3501 | 307/1166 | chr5 | 131704262 | |||
chr5:131730936 | A | C | 1 | a0008 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.322T>G | p.Ser108Ala | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/18 | 418/6568 | 322/3501 | 108/1166 | chr5 | 131730936 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:131670580 | C | T | 1 | a0001c0016 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2991G>A | p.Gly997Gly | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/18 | 3087/6568 | 2991/3501 | 997/1166 | chr5 | 131670580 | |||
chr5:131672017 | A | G | 1 | a0003c0003 | 10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.2427T>C | p.Asp809Asp | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2523/6568 | 2427/3501 | 809/1166 | chr5 | 131672017 | |||
chr5:131672053 | A | G | 1 | a0001c0008 | 2 | NA18940.hp2 NA19077.hp2 |
synonymous_variant | LOW | c.2391T>C | p.Thr797Thr | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2487/6568 | 2391/3501 | 797/1166 | chr5 | 131672053 | |||
chr5:131672094 | A | G | 1 | a0001c0004 | 6 | HG02155.hp2 HG03927.hp1 NA18940.hp1 others(3): Show |
synonymous_variant | LOW | c.2350T>C | p.Leu784Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 2446/6568 | 2350/3501 | 784/1166 | chr5 | 131672094 | |||
chr5:131672791 | C | T | 1 | a0002c0006 | 3 | HG01978.hp1 HG01981.hp2 HG02293.hp1 |
synonymous_variant | LOW | c.1653G>A | p.Thr551Thr | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/18 | 1749/6568 | 1653/3501 | 551/1166 | chr5 | 131672791 | |||
chr5:131706425 | C | T | 1 | a0001c0014 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.900G>A | p.Gly300Gly | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/18 | 996/6568 | 900/3501 | 300/1166 | chr5 | 131706425 | |||
chr5:131710588 | A | C | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.696T>G | p.Ser232Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/18 | 792/6568 | 696/3501 | 232/1166 | chr5 | 131710588 | |||
chr5:131719057 | G | A | 1 | a0001c0005 | 6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.459C>T | p.Ser153Ser | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/18 | 555/6568 | 459/3501 | 153/1166 | chr5 | 131719057 | |||
chr5:131719385 | A | G | 1 | a0001c0012 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.387T>C | p.Leu129Leu | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 4/18 | 483/6568 | 387/3501 | 129/1166 | chr5 | 131719385 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:131642181 | C | T | 1 | a0002c0002t0018 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2504G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2504 | chr5 | 131642181 | ||||||
chr5:131642256 | G | A | 1 | a0001c0001t0013 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2429C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2429 | chr5 | 131642256 | ||||||
chr5:131642310 | T | G | 4 | a0002c0002t0004 a0002c0002t0010 a0002c0006t0004 others(1): Show |
26 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2375A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2375 | chr5 | 131642310 | ||||||
chr5:131642439 | C | G | 3 | a0001c0001t0003 a0001c0001t0012 a0001c0013t0003 |
30 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2246G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 2246 | chr5 | 131642439 | ||||||
chr5:131642867 | C | CA | 7 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0021 others(4): Show |
25 | HG01099.hp1 HG01123.hp1 HG01261.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1817dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1817 | chr5 | 131642867 | ||||||
chr5:131642867 | CA | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(15): Show |
173 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1817delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1817 | chr5 | 131642867 | ||||||
chr5:131642867 | CAA | C | 3 | a0001c0001t0009 a0002c0002t0018 a0005c0009t0014 |
7 | HG02486.hp2 HG03041.hp1 NA18941.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1816_*1817delTT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1816 | chr5 | 131642867 | ||||||
chr5:131642966 | A | G | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1719T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1719 | chr5 | 131642966 | ||||||
chr5:131643485 | T | C | 2 | a0005c0009t0014 a0005c0009t0015 |
2 | HG02615.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1200A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1200 | chr5 | 131643485 | ||||||
chr5:131643638 | GA | G | 1 | a0001c0001t0008 | 5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1046delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1046 | chr5 | 131643638 | ||||||
chr5:131643639 | A | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
198 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1046T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1046 | chr5 | 131643639 | ||||||
chr5:131643674 | T | C | 1 | a0001c0001t0016 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1011 | chr5 | 131643674 | ||||||
chr5:131643680 | G | A | 1 | a0002c0002t0017 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 1005 | chr5 | 131643680 | ||||||
chr5:131643725 | T | C | 1 | a0001c0001t0022 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 960 | chr5 | 131643725 | ||||||
chr5:131644223 | C | T | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(1): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*462G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 462 | chr5 | 131644223 | ||||||
chr5:131644228 | T | C | 1 | a0002c0002t0018 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 457 | chr5 | 131644228 | ||||||
chr5:131644334 | G | A | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(14): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 351 | chr5 | 131644334 | ||||||
chr5:131644663 | T | C | 1 | a0001c0001t0023 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 18/18 | 22 | chr5 | 131644663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:131644843 | G | A | 2 | a0002c0002t0004g0053 a0002c0002t0004g0135 |
2 | HG03927.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3423-80C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644843 | |||||||
chr5:131644877 | G | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3423-114C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644877 | |||||||
chr5:131644890 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3423-127C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644890 | |||||||
chr5:131644953 | G | A | 1 | a0001c0001t0005g0280 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3423-190C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131644953 | |||||||
chr5:131645056 | G | A | 10 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 others(7): Show |
10 | HG00438.hp1 HG01261.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.3423-293C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645056 | |||||||
chr5:131645309 | C | CA | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.3423-547dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645309 | |||||||
chr5:131645336 | A | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3423-573T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645336 | |||||||
chr5:131645459 | A | G | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3423-696T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645459 | |||||||
chr5:131645561 | C | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3423-798G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645561 | |||||||
chr5:131645763 | C | A | 1 | a0002c0002t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3423-1000G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645763 | |||||||
chr5:131645765 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3423-1002T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645765 | |||||||
chr5:131645901 | A | C | 2 | a0002c0002t0004g0143 a0002c0002t0004g0284 |
2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3423-1138T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131645901 | |||||||
chr5:131646138 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3422+952A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646138 | |||||||
chr5:131646242 | T | C | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3422+848A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646242 | |||||||
chr5:131646425 | T | C | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3422+665A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646425 | |||||||
chr5:131646468 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3422+622G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646468 | |||||||
chr5:131646501 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.3422+589T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646501 | |||||||
chr5:131646688 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3422+402A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646688 | |||||||
chr5:131646720 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3422+370A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646720 | |||||||
chr5:131646741 | T | A | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3422+349A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646741 | |||||||
chr5:131646985 | T | C | 3 | a0001c0001t0001g0295 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01175.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3422+105A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646985 | |||||||
chr5:131646987 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3422+103T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131646987 | |||||||
chr5:131647075 | A | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.3422+15T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131647075 | |||||||
chr5:131647079 | C | T | 1 | a0006c0010t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3422+11G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 17/17 | chr5 | 131647079 | |||||||
chr5:131647356 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0007g0302 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3307-151A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647356 | |||||||
chr5:131647416 | C | CTT | 192 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(189): Show |
192 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.3307-213_3307-212d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647416 | |||||||
chr5:131647416 | C | CTTT | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-214_3307-212d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647416 | |||||||
chr5:131647559 | C | T | 4 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0060 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3307-354G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647559 | |||||||
chr5:131647631 | C | A | 2 | a0002c0002t0004g0007 a0002c0002t0004g0162 |
2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3307-426G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647631 | |||||||
chr5:131647677 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0290 |
3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3307-472G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647677 | |||||||
chr5:131647679 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3307-474A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647679 | |||||||
chr5:131647728 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3307-523T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647728 | |||||||
chr5:131647796 | T | C | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3307-591A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131647796 | |||||||
chr5:131648077 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3307-872G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648077 | |||||||
chr5:131648092 | G | A | 1 | a0003c0003t0002g0320 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3307-887C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648092 | |||||||
chr5:131648173 | T | TA | 156 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(153): Show |
156 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.3307-969dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648173 | |||||||
chr5:131648173 | TA | T | 13 | a0001c0001t0002g0055 a0001c0001t0002g0086 a0001c0001t0002g0099 others(10): Show |
13 | HG00639.hp1 HG01081.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.3307-969delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648173 | |||||||
chr5:131648310 | C | CA | 7 | a0001c0001t0003g0028 a0001c0001t0008g0019 a0001c0001t0008g0045 others(4): Show |
7 | HG01496.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3307-1106dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648310 | |||||||
chr5:131648428 | G | C | 1 | a0002c0002t0002g0005 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3307-1223C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648428 | |||||||
chr5:131648470 | T | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3307-1265A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648470 | |||||||
chr5:131648602 | A | T | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3307-1397T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648602 | |||||||
chr5:131648714 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3307-1509A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648714 | |||||||
chr5:131648824 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3307-1619G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648824 | |||||||
chr5:131648894 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0156 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3307-1689C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131648894 | |||||||
chr5:131649033 | T | C | 2 | a0002c0002t0002g0160 a0002c0002t0002g0161 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3307-1828A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649033 | |||||||
chr5:131649600 | G | A | 2 | a0002c0002t0004g0053 a0002c0002t0004g0135 |
2 | HG03927.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3306+2202C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649600 | |||||||
chr5:131649634 | A | C | 1 | a0001c0001t0002g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3306+2168T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649634 | |||||||
chr5:131649757 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3306+2045G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649757 | |||||||
chr5:131649758 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3306+2044A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649758 | |||||||
chr5:131649833 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3306+1969A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649833 | |||||||
chr5:131649952 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3306+1850C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131649952 | |||||||
chr5:131650004 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3306+1798T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650004 | |||||||
chr5:131650013 | A | G | 2 | a0001c0001t0003g0306 a0001c0001t0003g0309 |
2 | HG00639.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3306+1789T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650013 | |||||||
chr5:131650095 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3306+1707G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650095 | |||||||
chr5:131650619 | G | A | 1 | a0001c0012t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3306+1183C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650619 | |||||||
chr5:131650733 | T | G | 1 | a0002c0002t0002g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3306+1069A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650733 | |||||||
chr5:131650859 | T | C | 1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3306+943A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131650859 | |||||||
chr5:131651056 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3306+746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651056 | |||||||
chr5:131651086 | TA | T | 39 | a0001c0001t0001g0221 a0001c0001t0001g0303 a0001c0001t0003g0020 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3306+715delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651086 | |||||||
chr5:131651391 | C | G | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3306+411G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651391 | |||||||
chr5:131651481 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3306+321C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651481 | |||||||
chr5:131651538 | T | G | 1 | a0001c0001t0005g0280 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3306+264A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 16/17 | chr5 | 131651538 | |||||||
chr5:131652307 | G | C | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-308C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652307 | |||||||
chr5:131652308 | C | G | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-309G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652308 | |||||||
chr5:131652336 | A | G | 189 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(186): Show |
189 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(186): Show |
intron_variant | MODIFIER | c.3109-337T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652336 | |||||||
chr5:131652342 | A | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0228 a0001c0001t0001g0234 others(1): Show |
4 | HG00609.hp2 NA18957.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-343T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652342 | |||||||
chr5:131652450 | G | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-451C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652450 | |||||||
chr5:131652511 | C | G | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-512G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652511 | |||||||
chr5:131652512 | G | C | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3109-513C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652512 | |||||||
chr5:131652563 | G | A | 13 | a0001c0001t0003g0020 a0001c0001t0003g0031 a0001c0001t0003g0033 others(10): Show |
13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3109-564C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652563 | |||||||
chr5:131652620 | C | A | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-621G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652620 | |||||||
chr5:131652696 | A | T | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-697T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652696 | |||||||
chr5:131652759 | T | C | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-760A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652759 | |||||||
chr5:131652887 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-888G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652887 | |||||||
chr5:131652965 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-966T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131652965 | |||||||
chr5:131653002 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3109-1003T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653002 | |||||||
chr5:131653088 | G | A | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-1089C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653088 | |||||||
chr5:131653197 | TCAAAATA others(16): Show |
T | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3109-1221_3109-119 others(27): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653197 | |||||||
chr5:131653207 | C | G | 1 | a0002c0002t0004g0143 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3109-1208G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653207 | |||||||
chr5:131653262 | G | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.3109-1263C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653262 | |||||||
chr5:131653309 | G | A | 24 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(21): Show |
24 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3109-1310C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653309 | |||||||
chr5:131653526 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-1527G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653526 | |||||||
chr5:131653609 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-1610C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653609 | |||||||
chr5:131653653 | T | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3109-1654A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653653 | |||||||
chr5:131653733 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.3109-1734G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653733 | |||||||
chr5:131653766 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-1767G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653766 | |||||||
chr5:131653975 | C | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-1976G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653975 | |||||||
chr5:131653976 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-1977C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131653976 | |||||||
chr5:131654381 | T | C | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3109-2382A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654381 | |||||||
chr5:131654394 | C | T | 1 | a0001c0001t0007g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3109-2395G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654394 | |||||||
chr5:131654601 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-2602C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654601 | |||||||
chr5:131654651 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-2652A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654651 | |||||||
chr5:131654691 | T | C | 147 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
147 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.3109-2692A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654691 | |||||||
chr5:131654844 | G | A | 1 | a0002c0002t0002g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3109-2845C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654844 | |||||||
chr5:131654890 | G | T | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3109-2891C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654890 | |||||||
chr5:131654940 | A | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-2941T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654940 | |||||||
chr5:131654962 | C | T | 5 | a0001c0001t0002g0124 a0001c0001t0005g0077 a0001c0001t0005g0115 others(2): Show |
5 | NA18939.hp2 NA18998.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-2963G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654962 | |||||||
chr5:131654972 | C | T | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-2973G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131654972 | |||||||
chr5:131655084 | C | T | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3109-3085G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655084 | |||||||
chr5:131655202 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0290 |
3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3109-3203A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655202 | |||||||
chr5:131655277 | C | T | 5 | a0001c0001t0002g0124 a0001c0001t0005g0077 a0001c0001t0005g0115 others(2): Show |
5 | NA18939.hp2 NA18998.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-3278G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655277 | |||||||
chr5:131655659 | G | A | 4 | a0001c0001t0007g0060 a0001c0001t0007g0302 a0001c0001t0007g0323 others(1): Show |
4 | HG02630.hp1 HG03195.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-3660C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655659 | |||||||
chr5:131655752 | C | CA | 186 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(183): Show |
186 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.3109-3754dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655752 | |||||||
chr5:131655784 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-3785C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655784 | |||||||
chr5:131655937 | C | CA | 4 | a0001c0001t0001g0215 a0001c0001t0001g0296 a0001c0001t0001g0301 others(1): Show |
4 | HG02738.hp1 HG03704.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-3939dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655937 | |||||||
chr5:131655940 | A | C | 3 | a0001c0001t0001g0200 a0006c0010t0001g0205 a0006c0010t0001g0292 |
3 | HG03239.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3109-3941T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655940 | |||||||
chr5:131655941 | A | C | 7 | a0001c0001t0001g0177 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG00408.hp2 HG02040.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3109-3942T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655941 | |||||||
chr5:131655942 | C | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(115): Show |
118 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.3109-3943G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131655942 | |||||||
chr5:131656295 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-4296C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656295 | |||||||
chr5:131656336 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3109-4337G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656336 | |||||||
chr5:131656412 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3109-4413A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656412 | |||||||
chr5:131656427 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3109-4428A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656427 | |||||||
chr5:131656440 | G | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-4441C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656440 | |||||||
chr5:131656562 | T | G | 4 | a0001c0001t0007g0060 a0001c0001t0007g0302 a0001c0001t0007g0323 others(1): Show |
4 | HG02630.hp1 HG03195.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-4563A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656562 | |||||||
chr5:131656566 | G | A | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3109-4567C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656566 | |||||||
chr5:131656591 | T | G | 204 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3109-4592A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656591 | |||||||
chr5:131656600 | A | G | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-4601T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656600 | |||||||
chr5:131656603 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3109-4604T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656603 | |||||||
chr5:131656644 | GCTTTTGC others(24): Show |
G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-4676_3109-464 others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656644 | |||||||
chr5:131656739 | T | C | 204 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3109-4740A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656739 | |||||||
chr5:131656883 | T | C | 1 | a0001c0004t0001g0259 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3109-4884A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131656883 | |||||||
chr5:131657019 | C | CT | 57 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0172 others(54): Show |
57 | HG00544.hp1 HG00639.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.3109-5021dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657019 | |||||||
chr5:131657019 | CT | C | 111 | a0001c0001t0001g0257 a0001c0001t0002g0002 a0001c0001t0002g0004 others(108): Show |
113 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3109-5021delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657019 | |||||||
chr5:131657056 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.3109-5057G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657056 | |||||||
chr5:131657250 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-5251G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657250 | |||||||
chr5:131657369 | A | T | 2 | a0001c0001t0003g0028 a0001c0013t0003g0027 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3109-5370T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657369 | |||||||
chr5:131657431 | A | G | 204 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.3109-5432T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657431 | |||||||
chr5:131657736 | C | CA | 35 | a0001c0001t0001g0072 a0001c0001t0001g0171 a0001c0001t0002g0002 others(32): Show |
36 | HG01081.hp1 HG01175.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.3109-5738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657736 | C | CAA | 65 | a0001c0001t0001g0011 a0001c0001t0001g0057 a0001c0001t0001g0058 others(62): Show |
65 | HG00408.hp2 HG00639.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.3109-5739_3109-573 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657736 | C | CAAA | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
77 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.3109-5740_3109-573 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657736 | C | CAAAA | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0185 others(27): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.3109-5741_3109-573 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657736 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3109-5747_3109-573 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657736 | CAAAAAA | C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-5743_3109-573 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657736 | |||||||
chr5:131657783 | CGGATCTT others(8): Show |
C | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3109-5799_3109-578 others(19): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131657783 | |||||||
chr5:131658040 | C | CA | 21 | a0001c0001t0001g0010 a0001c0001t0001g0172 a0001c0001t0001g0193 others(18): Show |
21 | HG01081.hp1 HG01981.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3109-6042dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | |||||||
chr5:131658040 | C | CAA | 6 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(3): Show |
6 | HG01496.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-6043_3109-604 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | |||||||
chr5:131658040 | CA | C | 8 | a0001c0001t0001g0178 a0001c0001t0002g0106 a0001c0001t0003g0026 others(5): Show |
8 | HG00639.hp1 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-6042delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658040 | |||||||
chr5:131658122 | C | G | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3109-6123G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658122 | |||||||
chr5:131658217 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-6218T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658217 | |||||||
chr5:131658423 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3109-6424G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658423 | |||||||
chr5:131658634 | G | T | 6 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-6635C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658634 | |||||||
chr5:131658716 | G | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-6717C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658716 | |||||||
chr5:131658736 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.3109-6737C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658736 | |||||||
chr5:131658785 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-6786A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658785 | |||||||
chr5:131658907 | C | CA | 23 | a0001c0001t0002g0083 a0001c0001t0002g0094 a0001c0001t0002g0099 others(20): Show |
23 | HG00544.hp2 HG02040.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3109-6909dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAA | 20 | a0001c0001t0001g0206 a0001c0001t0002g0097 a0001c0001t0002g0123 others(17): Show |
20 | HG01069.hp2 HG01071.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.3109-6910_3109-690 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAA | 18 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0026 others(15): Show |
18 | HG00639.hp1 HG00642.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.3109-6911_3109-690 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAA | 61 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0001g0165 others(58): Show |
61 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.3109-6912_3109-690 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAAA | 54 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0056 others(51): Show |
54 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.3109-6913_3109-690 others(9): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAAAA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0221 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3109-6914_3109-690 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0180 a0001c0001t0007g0023 a0001c0001t0007g0024 |
3 | HG02109.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-6919_3109-690 others(15): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0007g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3109-6920_3109-690 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3109-6922_3109-690 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(14): Show |
17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.3109-6917_3109-690 others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131658907 | CAAAAAAA others(3): Show |
C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-6918_3109-690 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131658907 | |||||||
chr5:131659170 | G | A | 17 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(14): Show |
17 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3109-7171C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659170 | |||||||
chr5:131659172 | T | C | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-7173A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659172 | |||||||
chr5:131659191 | A | G | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3109-7192T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659191 | |||||||
chr5:131659600 | C | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3109-7601G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659600 | |||||||
chr5:131659619 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3109-7620G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659619 | |||||||
chr5:131659633 | G | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3109-7634C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659633 | |||||||
chr5:131659649 | C | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0041 a0001c0001t0003g0042 others(1): Show |
4 | HG00642.hp1 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-7650G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659649 | |||||||
chr5:131659688 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3109-7689A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659688 | |||||||
chr5:131659780 | T | C | 1 | a0001c0001t0005g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3109-7781A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131659780 | |||||||
chr5:131660451 | C | G | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-8452G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660451 | |||||||
chr5:131660467 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3109-8468T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660467 | |||||||
chr5:131660511 | T | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-8512A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660511 | |||||||
chr5:131660598 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0199 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3109-8599G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660598 | |||||||
chr5:131660755 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3109-8756G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660755 | |||||||
chr5:131660758 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.3109-8759T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660758 | |||||||
chr5:131660809 | G | A | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3109-8810C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660809 | |||||||
chr5:131660814 | T | C | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-8815A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660814 | |||||||
chr5:131660854 | G | A | 1 | a0001c0001t0022g0208 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3109-8855C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660854 | |||||||
chr5:131660869 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0020g0232 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3109-8870C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660869 | |||||||
chr5:131660939 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3109-8940C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131660939 | |||||||
chr5:131661062 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3109-9063T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661062 | |||||||
chr5:131661217 | GTT | G | 3 | a0001c0001t0001g0165 a0001c0001t0002g0098 a0001c0001t0007g0060 |
3 | HG03195.hp1 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661217 | |||||||
chr5:131661218 | T | TTG | 106 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(103): Show |
106 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTG | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(24): Show |
27 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTG | 6 | a0001c0001t0001g0169 a0001c0001t0001g0203 a0001c0001t0001g0303 others(3): Show |
6 | HG00741.hp2 HG01516.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(1): Show |
20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(3): Show |
16 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0022 others(13): Show |
16 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(5): Show |
3 | a0001c0001t0003g0021 a0001c0001t0003g0049 a0001c0014t0001g0326 |
3 | HG00642.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3109-9220_3109-921 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0003g0036 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0003g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(22): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(24): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(21): Show |
1 | a0005c0009t0015g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(32): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661218 | T | TTGTGTGT others(23): Show |
1 | a0005c0009t0014g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3109-9220_3109-921 others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661218 | |||||||
chr5:131661220 | T | G | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(197): Show |
200 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.3109-9221A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | |||||||
chr5:131661220 | T | TTG | 13 | a0001c0001t0002g0002 a0001c0001t0002g0081 a0001c0001t0002g0096 others(10): Show |
14 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3109-9223_3109-922 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | |||||||
chr5:131661220 | T | TTGTG | 3 | a0002c0002t0002g0082 a0002c0002t0002g0161 a0002c0002t0005g0127 |
3 | HG01255.hp1 HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3109-9225_3109-922 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661220 | |||||||
chr5:131661472 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.3108+8991C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661472 | |||||||
chr5:131661525 | G | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3108+8938C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661525 | |||||||
chr5:131661712 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0290 |
3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3108+8751G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661712 | |||||||
chr5:131661764 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3108+8699G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661764 | |||||||
chr5:131661768 | C | T | 1 | a0001c0001t0006g0258 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3108+8695G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661768 | |||||||
chr5:131661982 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0266 |
2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3108+8481G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131661982 | |||||||
chr5:131662060 | G | C | 10 | a0001c0001t0001g0064 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+8403C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662060 | |||||||
chr5:131662309 | G | GA | 12 | a0001c0001t0001g0185 a0001c0001t0002g0004 a0001c0001t0002g0054 others(9): Show |
12 | HG02135.hp2 HG02155.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.3108+8153dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662309 | |||||||
chr5:131662453 | C | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+8010G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662453 | |||||||
chr5:131662550 | A | G | 2 | a0001c0001t0002g0101 a0001c0001t0002g0159 |
2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3108+7913T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662550 | |||||||
chr5:131662574 | G | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3108+7889C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662574 | |||||||
chr5:131662733 | A | AT | 42 | a0001c0001t0001g0064 a0001c0001t0002g0081 a0001c0001t0002g0093 others(39): Show |
42 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.3108+7729dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | |||||||
chr5:131662733 | AT | A | 31 | a0001c0001t0001g0074 a0001c0001t0001g0165 a0001c0001t0001g0179 others(28): Show |
31 | HG00408.hp2 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.3108+7729delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | |||||||
chr5:131662733 | ATT | A | 127 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(124): Show |
127 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.3108+7728_3108+772 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662733 | |||||||
chr5:131662742 | T | A | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3108+7721A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662742 | |||||||
chr5:131662931 | C | T | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3108+7532G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662931 | |||||||
chr5:131662932 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3108+7531C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131662932 | |||||||
chr5:131663145 | T | A | 1 | a0001c0001t0001g0251 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3108+7318A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663145 | |||||||
chr5:131663198 | A | G | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3108+7265T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663198 | |||||||
chr5:131663270 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+7193A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663270 | |||||||
chr5:131663389 | A | G | 201 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.3108+7074T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663389 | |||||||
chr5:131663444 | C | T | 14 | a0001c0001t0003g0020 a0001c0001t0003g0031 a0001c0001t0003g0033 others(11): Show |
14 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3108+7019G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663444 | |||||||
chr5:131663526 | AAAG | A | 24 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(21): Show |
24 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.3108+6934_3108+693 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663526 | |||||||
chr5:131663569 | T | G | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+6894A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663569 | |||||||
chr5:131663684 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+6779A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663684 | |||||||
chr5:131663714 | G | C | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+6749C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663714 | |||||||
chr5:131663879 | G | C | 1 | a0001c0001t0009g0170 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3108+6584C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131663879 | |||||||
chr5:131664561 | G | C | 1 | a0002c0002t0004g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3108+5902C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664561 | |||||||
chr5:131664589 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+5874G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664589 | |||||||
chr5:131664634 | C | CA | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0064 others(44): Show |
47 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.3108+5828dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | |||||||
chr5:131664634 | C | CAA | 123 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(120): Show |
123 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.3108+5827_3108+582 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | |||||||
chr5:131664634 | C | CAAA | 28 | a0001c0001t0001g0058 a0001c0001t0001g0182 a0001c0001t0001g0188 others(25): Show |
28 | HG00438.hp2 HG01256.hp1 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.3108+5826_3108+582 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664634 | |||||||
chr5:131664826 | T | C | 10 | a0001c0001t0001g0064 a0001c0001t0007g0023 a0001c0001t0007g0024 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+5637A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664826 | |||||||
chr5:131664888 | A | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3108+5575T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664888 | |||||||
chr5:131664955 | GAT | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+5506_3108+550 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664955 | |||||||
chr5:131664961 | C | A | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.3108+5502G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664961 | |||||||
chr5:131664987 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3108+5476C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131664987 | |||||||
chr5:131665003 | A | G | 126 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
126 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.3108+5460T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665003 | |||||||
chr5:131665018 | A | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.3108+5445T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665018 | |||||||
chr5:131665131 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3108+5332C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665131 | |||||||
chr5:131665179 | A | T | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3108+5284T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665179 | |||||||
chr5:131665317 | T | C | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3108+5146A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665317 | |||||||
chr5:131665449 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3108+5014C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665449 | |||||||
chr5:131665511 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3108+4952A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665511 | |||||||
chr5:131665585 | T | G | 2 | a0001c0001t0003g0036 a0001c0001t0007g0302 |
2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3108+4878A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665585 | |||||||
chr5:131665594 | G | GT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0074 a0001c0001t0001g0260 others(6): Show |
9 | HG02615.hp1 HG03041.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+4868dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665594 | |||||||
chr5:131665682 | C | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3108+4781G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665682 | |||||||
chr5:131665683 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3108+4780T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665683 | |||||||
chr5:131665692 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3108+4771G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665692 | |||||||
chr5:131665695 | T | C | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3108+4768A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665695 | |||||||
chr5:131665714 | C | T | 2 | a0001c0001t0001g0202 a0002c0002t0002g0283 |
2 | HG01433.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3108+4749G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665714 | |||||||
chr5:131665898 | A | AT | 41 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0182 others(38): Show |
41 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3108+4564_3108+456 others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | |||||||
chr5:131665898 | AC | A | 55 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0171 others(52): Show |
55 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.3108+4564delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | |||||||
chr5:131665898 | ACT | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3108+4563_3108+456 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665898 | |||||||
chr5:131665899 | C | CT | 7 | a0001c0001t0002g0085 a0001c0001t0002g0124 a0001c0001t0005g0287 others(4): Show |
7 | HG02273.hp2 HG03927.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.3108+4563dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665899 | |||||||
chr5:131665899 | C | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3108+4564G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665899 | |||||||
chr5:131665941 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.3108+4522C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665941 | |||||||
chr5:131665963 | G | A | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+4500C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131665963 | |||||||
chr5:131666057 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3108+4406A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666057 | |||||||
chr5:131666138 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+4325G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666138 | |||||||
chr5:131666139 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3108+4324C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666139 | |||||||
chr5:131666218 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3108+4245A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666218 | |||||||
chr5:131666504 | A | G | 1 | a0001c0001t0002g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3108+3959T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666504 | |||||||
chr5:131666818 | A | C | 3 | a0001c0001t0001g0064 a0001c0014t0001g0326 a0001c0016t0001g0063 |
3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3108+3645T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666818 | |||||||
chr5:131666834 | G | A | 1 | a0003c0003t0002g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3108+3629C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666834 | |||||||
chr5:131666850 | G | A | 1 | a0001c0001t0009g0013 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3108+3613C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666850 | |||||||
chr5:131666905 | C | T | 6 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0060 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+3558G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131666905 | |||||||
chr5:131667099 | A | G | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(300): Show |
305 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(302): Show |
intron_variant | MODIFIER | c.3108+3364T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667099 | |||||||
chr5:131667294 | A | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3108+3169T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667294 | |||||||
chr5:131667336 | G | C | 1 | a0001c0005t0001g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3108+3127C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667336 | |||||||
chr5:131667510 | G | A | 1 | a0001c0012t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3108+2953C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667510 | |||||||
chr5:131667573 | T | G | 1 | a0001c0001t0003g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3108+2890A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | |||||||
chr5:131667573 | TTTTG | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.3108+2886_3108+288 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | |||||||
chr5:131667573 | TTTTGTTT others(5): Show |
T | 4 | a0002c0002t0004g0130 a0002c0002t0004g0131 a0002c0002t0004g0132 others(1): Show |
4 | NA18966.hp2 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+2878_3108+288 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667573 | |||||||
chr5:131667649 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+2814G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667649 | |||||||
chr5:131667672 | T | TCTA | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+2788_3108+279 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667672 | |||||||
chr5:131667747 | C | A | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3108+2716G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131667747 | |||||||
chr5:131668118 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3108+2345G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668118 | |||||||
chr5:131668195 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+2268T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668195 | |||||||
chr5:131668292 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3108+2171A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668292 | |||||||
chr5:131668345 | T | C | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3108+2118A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668345 | |||||||
chr5:131668434 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3108+2029G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668434 | |||||||
chr5:131668465 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3108+1998G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668465 | |||||||
chr5:131668556 | G | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3108+1907C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668556 | |||||||
chr5:131668602 | T | C | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+1861A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668602 | |||||||
chr5:131668608 | C | T | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3108+1855G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668608 | |||||||
chr5:131668820 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3108+1643C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668820 | |||||||
chr5:131668883 | T | G | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3108+1580A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668883 | |||||||
chr5:131668953 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.3108+1510C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131668953 | |||||||
chr5:131669241 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0155 |
2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.3108+1222C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669241 | |||||||
chr5:131669268 | C | A | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+1195G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669268 | |||||||
chr5:131669273 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3108+1190C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669273 | |||||||
chr5:131669488 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.3108+975T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669488 | |||||||
chr5:131669580 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3108+883G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669580 | |||||||
chr5:131669581 | G | A | 4 | a0002c0002t0004g0130 a0002c0002t0004g0131 a0002c0002t0004g0132 others(1): Show |
4 | NA18966.hp2 NA18978.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+882C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669581 | |||||||
chr5:131669590 | A | G | 1 | a0002c0002t0002g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3108+873T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669590 | |||||||
chr5:131669618 | T | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3108+845A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669618 | |||||||
chr5:131669645 | T | A | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3108+818A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669645 | |||||||
chr5:131669666 | C | A | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+797G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669666 | |||||||
chr5:131669680 | A | C | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0224 others(2): Show |
5 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.3108+783T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669680 | |||||||
chr5:131669827 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+636A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669827 | |||||||
chr5:131669830 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3108+633G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669830 | |||||||
chr5:131669907 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3108+556A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669907 | |||||||
chr5:131669917 | C | CA | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3108+545dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669917 | |||||||
chr5:131669945 | C | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.3108+518G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669945 | |||||||
chr5:131669990 | C | A | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+473G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669990 | |||||||
chr5:131669991 | T | C | 2 | a0002c0002t0004g0007 a0002c0002t0004g0162 |
2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3108+472A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131669991 | |||||||
chr5:131670389 | A | G | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.3108+74T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 15/17 | chr5 | 131670389 | |||||||
chr5:131670651 | A | C | 1 | a0001c0001t0005g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2940-20T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670651 | |||||||
chr5:131670663 | T | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.2940-32A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670663 | |||||||
chr5:131670688 | T | TA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0185 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940-58dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670688 | |||||||
chr5:131670703 | G | C | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2940-72C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670703 | |||||||
chr5:131670854 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2940-223G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670854 | |||||||
chr5:131670872 | A | T | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2940-241T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670872 | |||||||
chr5:131670919 | A | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2940-288T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670919 | |||||||
chr5:131670938 | A | G | 2 | a0002c0002t0004g0120 a0002c0002t0004g0144 |
2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2940-307T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 14/17 | chr5 | 131670938 | |||||||
chr5:131673051 | G | GT | 17 | a0001c0001t0001g0206 a0001c0001t0001g0212 a0001c0001t0001g0246 others(14): Show |
17 | HG00738.hp2 HG01884.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.1520-128dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673051 | |||||||
chr5:131673051 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1520-127C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673051 | |||||||
chr5:131673058 | T | G | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1520-134A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673058 | |||||||
chr5:131673192 | C | T | 201 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.1520-268G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673192 | |||||||
chr5:131673657 | G | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1520-733C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673657 | |||||||
chr5:131673689 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1520-765T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673689 | |||||||
chr5:131673708 | G | A | 1 | a0001c0001t0007g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520-784C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673708 | |||||||
chr5:131673773 | C | T | 1 | a0001c0001t0005g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1520-849G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673773 | |||||||
chr5:131673886 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520-962T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673886 | |||||||
chr5:131673972 | G | A | 6 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520-1048C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673972 | |||||||
chr5:131673985 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1520-1061C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131673985 | |||||||
chr5:131674220 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1520-1296T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674220 | |||||||
chr5:131674535 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1520-1611G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674535 | |||||||
chr5:131674562 | C | T | 2 | a0002c0002t0004g0143 a0002c0002t0004g0284 |
2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1520-1638G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674562 | |||||||
chr5:131674791 | A | G | 5 | a0001c0001t0002g0004 a0001c0001t0002g0054 a0001c0001t0002g0104 others(2): Show |
5 | NA18941.hp1 NA18946.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520-1867T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674791 | |||||||
chr5:131674818 | C | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0182 others(32): Show |
35 | HG00544.hp1 HG00609.hp2 HG01978.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520-1894G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674818 | |||||||
chr5:131674819 | TTTACAAA others(2): Show |
T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0182 others(32): Show |
35 | HG00544.hp1 HG00609.hp2 HG01978.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520-1904_1520-189 others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674819 | |||||||
chr5:131674953 | A | G | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1520-2029T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131674953 | |||||||
chr5:131675292 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1520-2368G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675292 | |||||||
chr5:131675642 | A | G | 1 | a0001c0001t0001g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1519+2061T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675642 | |||||||
chr5:131675688 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1519+2015C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675688 | |||||||
chr5:131675890 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1519+1813G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131675890 | |||||||
chr5:131676198 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1519+1505C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676198 | |||||||
chr5:131676212 | C | T | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1519+1491G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676212 | |||||||
chr5:131676305 | A | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1519+1398T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676305 | |||||||
chr5:131676311 | C | A | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1519+1392G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676311 | |||||||
chr5:131676314 | T | C | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1519+1389A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676314 | |||||||
chr5:131676330 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1519+1373C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676330 | |||||||
chr5:131676476 | G | C | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1519+1227C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676476 | |||||||
chr5:131676538 | G | A | 4 | a0001c0001t0001g0303 a0004c0007t0001g0176 a0004c0007t0001g0183 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1519+1165C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676538 | |||||||
chr5:131676565 | C | T | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1519+1138G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676565 | |||||||
chr5:131676678 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1519+1025C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676678 | |||||||
chr5:131676726 | C | G | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1519+977G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131676726 | |||||||
chr5:131677170 | C | T | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1519+533G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677170 | |||||||
chr5:131677341 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1519+362A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677341 | |||||||
chr5:131677597 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1519+106A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 13/17 | chr5 | 131677597 | |||||||
chr5:131677914 | A | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1350-42T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131677914 | |||||||
chr5:131677924 | A | AG | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1350-53dupC | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131677924 | |||||||
chr5:131678057 | G | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1350-185C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678057 | |||||||
chr5:131678122 | G | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1350-250C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678122 | |||||||
chr5:131678690 | A | G | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(300): Show |
305 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(302): Show |
intron_variant | MODIFIER | c.1349+339T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678690 | |||||||
chr5:131678722 | T | C | 1 | a0001c0001t0003g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1349+307A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131678722 | |||||||
chr5:131679002 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1349+27T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 12/17 | chr5 | 131679002 | |||||||
chr5:131679214 | A | T | 1 | a0001c0001t0006g0241 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1203-39T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679214 | |||||||
chr5:131679296 | A | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-121T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679296 | |||||||
chr5:131679297 | A | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-122T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679297 | |||||||
chr5:131679482 | A | G | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1203-307T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679482 | |||||||
chr5:131679510 | G | A | 5 | a0001c0001t0007g0060 a0001c0001t0007g0302 a0001c0001t0007g0323 others(2): Show |
5 | HG02630.hp1 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203-335C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679510 | |||||||
chr5:131679631 | T | C | 3 | a0001c0005t0001g0073 a0001c0005t0006g0066 a0001c0005t0006g0071 |
3 | HG02572.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1203-456A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679631 | |||||||
chr5:131679653 | A | G | 129 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
129 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1203-478T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679653 | |||||||
chr5:131679870 | A | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1203-695T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679870 | |||||||
chr5:131679921 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0005g0080 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1203-746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131679921 | |||||||
chr5:131680082 | T | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1203-907A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680082 | |||||||
chr5:131680246 | A | G | 4 | a0002c0002t0002g0082 a0002c0002t0002g0141 a0002c0002t0002g0289 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-1071T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680246 | |||||||
chr5:131680486 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-1311A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131680486 | |||||||
chr5:131681019 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0266 |
2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1203-1844G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681019 | |||||||
chr5:131681245 | C | T | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1203-2070G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681245 | |||||||
chr5:131681663 | G | GA | 201 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.1203-2489dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681663 | |||||||
chr5:131681762 | T | TA | 94 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(91): Show |
94 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1203-2588dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | |||||||
chr5:131681762 | T | TAA | 68 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
68 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1203-2589_1203-258 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | |||||||
chr5:131681762 | T | TAAA | 15 | a0001c0001t0001g0165 a0001c0001t0001g0199 a0001c0001t0001g0211 others(12): Show |
15 | HG01081.hp1 HG01978.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203-2590_1203-258 others(7): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681762 | |||||||
chr5:131681796 | A | G | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1203-2621T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131681796 | |||||||
chr5:131682138 | TATAA | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-2967_1203-296 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682138 | |||||||
chr5:131682211 | A | C | 12 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0074 others(9): Show |
12 | HG01081.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1203-3036T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682211 | |||||||
chr5:131682233 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1203-3058T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682233 | |||||||
chr5:131682258 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1203-3083A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682258 | |||||||
chr5:131682321 | T | C | 4 | a0002c0002t0002g0125 a0002c0002t0002g0163 a0002c0002t0002g0273 others(1): Show |
4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-3146A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682321 | |||||||
chr5:131682522 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0264 |
3 | HG02165.hp2 HG04184.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1203-3347G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682522 | |||||||
chr5:131682548 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1203-3373C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682548 | |||||||
chr5:131682711 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1203-3536G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682711 | |||||||
chr5:131682716 | C | CA | 15 | a0001c0001t0001g0185 a0001c0001t0003g0043 a0001c0001t0006g0241 others(12): Show |
15 | HG01884.hp1 HG02056.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1203-3542dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682716 | |||||||
chr5:131682876 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1203-3701G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682876 | |||||||
chr5:131682954 | TA | T | 15 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(12): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203-3780delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682954 | |||||||
chr5:131682996 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1203-3821G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131682996 | |||||||
chr5:131683085 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1203-3910T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683085 | |||||||
chr5:131683414 | G | A | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1203-4239C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683414 | |||||||
chr5:131683504 | A | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1203-4329T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683504 | |||||||
chr5:131683552 | C | CA | 48 | a0001c0001t0001g0064 a0001c0001t0001g0165 a0001c0001t0001g0193 others(45): Show |
48 | HG00544.hp2 HG01070.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1203-4378dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | |||||||
chr5:131683552 | C | CAA | 6 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0001g0074 others(3): Show |
6 | HG02280.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-4379_1203-437 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | |||||||
chr5:131683552 | CA | C | 11 | a0001c0001t0007g0302 a0001c0014t0001g0326 a0003c0003t0002g0311 others(8): Show |
11 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1203-4378delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683552 | |||||||
chr5:131683633 | A | G | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1203-4458T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683633 | |||||||
chr5:131683668 | G | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-4493C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683668 | |||||||
chr5:131683809 | A | G | 6 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-4634T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131683809 | |||||||
chr5:131684126 | C | A | 1 | a0001c0001t0003g0307 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203-4951G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684126 | |||||||
chr5:131684150 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1203-4975T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684150 | |||||||
chr5:131684151 | T | C | 2 | a0001c0004t0001g0061 a0001c0004t0001g0062 |
2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1203-4976A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684151 | |||||||
chr5:131684178 | A | G | 2 | a0002c0002t0002g0003 a0002c0002t0002g0005 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1203-5003T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684178 | |||||||
chr5:131684218 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1203-5043C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684218 | |||||||
chr5:131684396 | A | C | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1203-5221T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684396 | |||||||
chr5:131684402 | A | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0054 others(45): Show |
49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-5227T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684402 | |||||||
chr5:131684409 | A | G | 19 | a0001c0001t0002g0113 a0001c0001t0002g0124 a0001c0001t0002g0154 others(16): Show |
19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1203-5234T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684409 | |||||||
chr5:131684575 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1203-5400G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684575 | |||||||
chr5:131684589 | C | A | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1203-5414G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684589 | |||||||
chr5:131684643 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1203-5468C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684643 | |||||||
chr5:131684653 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1203-5478A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131684653 | |||||||
chr5:131685120 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1203-5945G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685120 | |||||||
chr5:131685360 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1203-6185T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685360 | |||||||
chr5:131685448 | C | CT | 198 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(195): Show |
199 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(196): Show |
intron_variant | MODIFIER | c.1203-6274dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685448 | |||||||
chr5:131685563 | T | C | 1 | a0001c0001t0003g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1203-6388A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685563 | |||||||
chr5:131685672 | T | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1203-6497A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685672 | |||||||
chr5:131685803 | T | TA | 259 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(256): Show |
260 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(257): Show |
intron_variant | MODIFIER | c.1203-6629dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685803 | |||||||
chr5:131685803 | T | TAA | 12 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0003c0003t0002g0311 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1203-6630_1203-662 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685803 | |||||||
chr5:131685940 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1203-6765A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131685940 | |||||||
chr5:131686358 | T | A | 11 | a0001c0001t0002g0004 a0001c0001t0002g0054 a0001c0001t0002g0076 others(8): Show |
11 | HG02135.hp2 HG02155.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1203-7183A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686358 | |||||||
chr5:131686492 | G | A | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203-7317C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686492 | |||||||
chr5:131686897 | A | G | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203-7722T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686897 | |||||||
chr5:131686923 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0190 a0001c0001t0001g0218 others(1): Show |
4 | HG00733.hp1 HG01070.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-7748G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686923 | |||||||
chr5:131686938 | C | A | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1203-7763G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131686938 | |||||||
chr5:131687056 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0007g0302 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1203-7881A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687056 | |||||||
chr5:131687348 | C | T | 1 | a0002c0002t0004g0130 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1203-8173G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687348 | |||||||
chr5:131687465 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0054 others(45): Show |
49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-8290G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687465 | |||||||
chr5:131687615 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1203-8440G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687615 | |||||||
chr5:131687806 | G | C | 2 | a0001c0001t0003g0028 a0001c0013t0003g0027 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1203-8631C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131687806 | |||||||
chr5:131688101 | T | TA | 48 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0054 others(45): Show |
49 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1203-8927dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688101 | |||||||
chr5:131688101 | TA | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203-8927delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688101 | |||||||
chr5:131688289 | T | TA | 43 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0002g0055 others(40): Show |
43 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.1203-9115dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688289 | |||||||
chr5:131688289 | TA | T | 13 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0074 others(10): Show |
13 | HG02280.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1203-9115delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688289 | |||||||
chr5:131688375 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-9200G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688375 | |||||||
chr5:131688662 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1203-9487A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688662 | |||||||
chr5:131688702 | T | TA | 139 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(136): Show |
139 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.1203-9528dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688702 | |||||||
chr5:131688937 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1203-9762G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131688937 | |||||||
chr5:131689081 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1202+9836C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689081 | |||||||
chr5:131689152 | C | CA | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1202+9764dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689152 | |||||||
chr5:131689778 | A | G | 320 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(317): Show |
322 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(319): Show |
intron_variant | MODIFIER | c.1202+9139T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689778 | |||||||
chr5:131689849 | A | T | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1202+9068T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131689849 | |||||||
chr5:131690011 | G | A | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1202+8906C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690011 | |||||||
chr5:131690080 | G | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+8837C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690080 | |||||||
chr5:131690119 | A | T | 2 | a0002c0002t0004g0007 a0002c0002t0004g0162 |
2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1202+8798T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690119 | |||||||
chr5:131690127 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1202+8790C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690127 | |||||||
chr5:131690131 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+8786C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690131 | |||||||
chr5:131690146 | C | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1202+8771G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690146 | |||||||
chr5:131690397 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1202+8520A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690397 | |||||||
chr5:131690483 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1202+8434T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690483 | |||||||
chr5:131690525 | G | A | 17 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0187 others(14): Show |
17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1202+8392C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690525 | |||||||
chr5:131690598 | G | A | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+8319C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690598 | |||||||
chr5:131690625 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01993.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1202+8292G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690625 | |||||||
chr5:131690697 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1202+8220C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690697 | |||||||
chr5:131690897 | C | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1202+8020G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690897 | |||||||
chr5:131690933 | A | G | 1 | a0001c0001t0007g0323 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1202+7984T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131690933 | |||||||
chr5:131691293 | G | C | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1202+7624C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691293 | |||||||
chr5:131691469 | A | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+7448T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691469 | |||||||
chr5:131691498 | A | T | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1202+7419T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691498 | |||||||
chr5:131691541 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1202+7376C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691541 | |||||||
chr5:131691786 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1202+7131C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691786 | |||||||
chr5:131691994 | A | G | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1202+6923T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131691994 | |||||||
chr5:131692040 | A | G | 7 | a0001c0001t0002g0094 a0001c0001t0002g0098 a0001c0001t0002g0101 others(4): Show |
7 | NA18940.hp2 NA18953.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+6877T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692040 | |||||||
chr5:131692149 | A | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1202+6768T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692149 | |||||||
chr5:131692156 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+6761C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692156 | |||||||
chr5:131692188 | T | C | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202+6729A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692188 | |||||||
chr5:131692311 | C | T | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1202+6606G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692311 | |||||||
chr5:131692324 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1202+6593T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692324 | |||||||
chr5:131692333 | G | A | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1202+6584C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692333 | |||||||
chr5:131692465 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+6452T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692465 | |||||||
chr5:131692503 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1202+6414T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692503 | |||||||
chr5:131692787 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1202+6130G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131692787 | |||||||
chr5:131693021 | T | A | 7 | a0001c0001t0001g0322 a0001c0001t0005g0078 a0001c0001t0005g0114 others(4): Show |
7 | HG01261.hp1 HG02486.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5896A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693021 | |||||||
chr5:131693230 | T | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1202+5687A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693230 | |||||||
chr5:131693260 | TA | T | 11 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0003g0304 others(8): Show |
11 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1202+5656delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693260 | |||||||
chr5:131693277 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1202+5640A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693277 | |||||||
chr5:131693289 | AATATATA others(29): Show |
A | 2 | a0001c0004t0001g0233 a0001c0004t0001g0259 |
2 | HG02155.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1202+5592_1202+562 others(40): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693289 | |||||||
chr5:131693297 | C | CAT | 3 | a0001c0001t0002g0086 a0002c0002t0002g0005 a0002c0002t0002g0141 |
3 | HG00438.hp1 HG03209.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1202+5618_1202+561 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | |||||||
chr5:131693297 | C | CATATATA others(35): Show |
1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1202+5619_1202+562 others(46): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | |||||||
chr5:131693297 | CATAT | C | 8 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0225 others(5): Show |
8 | HG01516.hp1 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202+5616_1202+561 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693297 | |||||||
chr5:131693301 | T | TATATATA others(19): Show |
2 | a0001c0001t0001g0264 a0001c0001t0006g0258 |
2 | NA18962.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1202+5615_1202+561 others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693301 | |||||||
chr5:131693303 | T | TATATATA others(1): Show |
10 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0002g0055 others(7): Show |
10 | HG01081.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693303 | T | TATATATA others(15): Show |
1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(26): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693303 | T | TATATATA others(3): Show |
4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0223 others(1): Show |
4 | HG00408.hp2 HG01433.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693303 | T | TATATATA others(17): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0239 |
2 | HG00438.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1202+5613_1202+561 others(28): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693303 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693303 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0212 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1202+5613_1202+561 others(23): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693303 | |||||||
chr5:131693305 | T | TATATATA others(1): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+5611_1202+561 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693305 | |||||||
chr5:131693307 | T | TATATAC | 4 | a0001c0001t0001g0236 a0001c0001t0001g0295 a0001c0001t0003g0033 others(1): Show |
4 | HG01175.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+5609_1202+561 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693307 | |||||||
chr5:131693307 | T | TATATACA others(29): Show |
3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1202+5609_1202+561 others(40): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693307 | |||||||
chr5:131693309 | T | TATAC | 7 | a0001c0001t0001g0222 a0001c0001t0001g0303 a0001c0001t0008g0019 others(4): Show |
7 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5607_1202+560 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | |||||||
chr5:131693309 | TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0193 a0001c0016t0001g0063 |
3 | HG02559.hp2 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | |||||||
chr5:131693309 | TATATATA others(17): Show |
T | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202+5584_1202+560 others(28): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693309 | |||||||
chr5:131693311 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+5606A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | |||||||
chr5:131693311 | T | TAC | 22 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0187 others(19): Show |
22 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+5605_1202+560 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | |||||||
chr5:131693311 | T | TACATATA others(9): Show |
1 | a0001c0001t0001g0224 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1202+5605_1202+560 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | |||||||
chr5:131693311 | TATATAC | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(26): Show |
29 | HG00609.hp1 HG00639.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | |||||||
chr5:131693311 | TATATACA others(15): Show |
T | 9 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+5584_1202+560 others(26): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693311 | |||||||
chr5:131693313 | T | C | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(79): Show |
82 | HG00544.hp1 HG00609.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1202+5604A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693313 | |||||||
chr5:131693315 | TAC | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0171 others(59): Show |
62 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1202+5600_1202+560 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693315 | |||||||
chr5:131693317 | C | T | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(130): Show |
134 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.1202+5600G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693317 | |||||||
chr5:131693319 | C | T | 147 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(144): Show |
147 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1202+5598G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693319 | |||||||
chr5:131693321 | T | C | 5 | a0001c0001t0001g0236 a0001c0001t0001g0295 a0001c0001t0003g0033 others(2): Show |
5 | HG00733.hp2 HG01175.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+5596A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693321 | |||||||
chr5:131693323 | T | C | 6 | a0001c0001t0001g0222 a0001c0001t0008g0019 a0001c0001t0008g0045 others(3): Show |
6 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+5594A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693323 | |||||||
chr5:131693325 | T | C | 22 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0187 others(19): Show |
22 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+5592A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693325 | |||||||
chr5:131693327 | T | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0174 others(19): Show |
22 | HG00544.hp1 HG01099.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1202+5590A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693327 | |||||||
chr5:131693329 | T | C | 66 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0171 others(63): Show |
66 | HG00609.hp2 HG00642.hp1 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.1202+5588A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693329 | |||||||
chr5:131693331 | T | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0225 others(4): Show |
7 | HG01516.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202+5586A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693331 | |||||||
chr5:131693333 | C | CACATATA others(3): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00738.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1202+5583_1202+558 others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CACATATA others(7): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1202+5583_1202+558 others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CAT | 27 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0269 others(24): Show |
28 | HG00642.hp2 HG01257.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1202+5582_1202+558 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CATAT | 30 | a0001c0001t0001g0212 a0001c0001t0002g0083 a0001c0001t0002g0085 others(27): Show |
31 | HG00408.hp1 HG00738.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1202+5580_1202+558 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CATATAT | 14 | a0001c0001t0002g0084 a0001c0001t0002g0086 a0001c0001t0002g0090 others(11): Show |
14 | HG01123.hp1 HG01261.hp1 HG02735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1202+5578_1202+558 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CATATATA others(1): Show |
7 | a0001c0001t0002g0055 a0001c0001t0002g0070 a0001c0001t0002g0151 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5576_1202+558 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | CATATATA others(49): Show |
1 | a0001c0001t0005g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1202+5583_1202+558 others(60): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | C | T | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(136): Show |
139 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1202+5584G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | CAT | C | 14 | a0001c0001t0001g0064 a0001c0001t0001g0264 a0001c0001t0007g0302 others(11): Show |
14 | HG01261.hp2 HG01433.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202+5582_1202+558 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693333 | CATATAT | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0002c0002t0002g0158 others(1): Show |
4 | HG00544.hp2 HG02165.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+5578_1202+558 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693333 | |||||||
chr5:131693335 | T | C | 8 | a0002c0002t0002g0148 a0003c0003t0002g0311 a0003c0003t0002g0313 others(5): Show |
8 | HG00733.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+5582A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | |||||||
chr5:131693335 | T | TATATATA others(5): Show |
1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+5581_1202+558 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | |||||||
chr5:131693335 | T | TATATATA others(53): Show |
1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1202+5581_1202+558 others(64): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693335 | |||||||
chr5:131693337 | T | C | 3 | a0003c0003t0002g0312 a0003c0003t0002g0317 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1202+5580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693337 | |||||||
chr5:131693340 | A | ATATG | 7 | a0001c0001t0002g0094 a0001c0001t0002g0098 a0001c0001t0002g0101 others(4): Show |
7 | NA18940.hp2 NA18953.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+5576_1202+557 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693340 | |||||||
chr5:131693344 | A | G | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+5573T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693344 | |||||||
chr5:131693346 | A | G | 3 | a0001c0001t0001g0064 a0001c0014t0001g0326 a0001c0016t0001g0063 |
3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+5571T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693346 | |||||||
chr5:131693348 | A | ATATATG | 3 | a0001c0001t0002g0099 a0001c0001t0002g0167 a0001c0001t0002g0276 |
3 | NA18949.hp1 NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1202+5568_1202+556 others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693348 | |||||||
chr5:131693348 | A | G | 3 | a0001c0001t0002g0097 a0001c0001t0002g0107 a0002c0002t0018g0059 |
3 | HG02486.hp2 NA18960.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1202+5569T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693348 | |||||||
chr5:131693349 | T | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1202+5568A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693349 | |||||||
chr5:131693372 | A | T | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+5545T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693372 | |||||||
chr5:131693475 | T | C | 9 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+5442A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693475 | |||||||
chr5:131693513 | C | T | 37 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(34): Show |
37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1202+5404G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693513 | |||||||
chr5:131693770 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1202+5147T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693770 | |||||||
chr5:131693866 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+5051C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693866 | |||||||
chr5:131693990 | T | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1202+4927A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131693990 | |||||||
chr5:131694364 | T | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+4553A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694364 | |||||||
chr5:131694392 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1202+4525C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694392 | |||||||
chr5:131694459 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1202+4458C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694459 | |||||||
chr5:131694602 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1202+4315C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694602 | |||||||
chr5:131694635 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0224 others(1): Show |
4 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+4282G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694635 | |||||||
chr5:131694669 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1202+4248A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694669 | |||||||
chr5:131694702 | A | G | 1 | a0001c0001t0007g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1202+4215T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694702 | |||||||
chr5:131694879 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1202+4038G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131694879 | |||||||
chr5:131695060 | G | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0030 a0001c0001t0023g0229 |
3 | HG01167.hp2 HG01169.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1202+3857C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695060 | |||||||
chr5:131695104 | C | CAAAT | 5 | a0001c0001t0002g0081 a0002c0002t0002g0003 a0002c0002t0002g0289 others(2): Show |
5 | HG02615.hp1 HG02976.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202+3809_1202+381 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695104 | C | CAAATAAA others(9): Show |
1 | a0002c0002t0005g0127 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1202+3797_1202+381 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695104 | CAAAT | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(174): Show |
178 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1202+3809_1202+381 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695104 | CAAATAAA others(1): Show |
C | 93 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0223 others(90): Show |
94 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.1202+3805_1202+381 others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695104 | CAAATAAA others(5): Show |
C | 9 | a0001c0001t0001g0212 a0001c0001t0001g0322 a0001c0001t0002g0107 others(6): Show |
9 | HG01496.hp1 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+3801_1202+381 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695104 | CAAATAAA others(9): Show |
C | 1 | a0002c0002t0002g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+3797_1202+381 others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695104 | |||||||
chr5:131695152 | T | G | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+3765A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695152 | |||||||
chr5:131695153 | A | AAAGC | 4 | a0001c0001t0001g0064 a0001c0001t0007g0302 a0001c0001t0007g0323 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+3760_1202+376 others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | |||||||
chr5:131695153 | A | AAATAAAT others(5): Show |
1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1202+3763_1202+376 others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | |||||||
chr5:131695153 | A | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1202+3764T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695153 | |||||||
chr5:131695268 | T | C | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(197): Show |
200 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.1202+3649A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695268 | |||||||
chr5:131695499 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+3418C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695499 | |||||||
chr5:131695809 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+3108C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695809 | |||||||
chr5:131695952 | G | A | 1 | a0002c0002t0004g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1202+2965C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131695952 | |||||||
chr5:131696140 | A | G | 3 | a0001c0001t0001g0064 a0001c0014t0001g0326 a0001c0016t0001g0063 |
3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1202+2777T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696140 | |||||||
chr5:131696419 | TAA | T | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202+2496_1202+249 others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696419 | |||||||
chr5:131696489 | C | T | 8 | a0001c0001t0002g0055 a0001c0001t0002g0070 a0001c0005t0001g0067 others(5): Show |
8 | HG01081.hp1 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+2428G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696489 | |||||||
chr5:131696717 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0155 |
2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1202+2200C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696717 | |||||||
chr5:131696875 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0007g0060 a0001c0001t0007g0302 others(4): Show |
7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+2042T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696875 | |||||||
chr5:131696879 | T | G | 1 | a0004c0007t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1202+2038A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696879 | |||||||
chr5:131696940 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1202+1977C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696940 | |||||||
chr5:131696952 | A | G | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1202+1965T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131696952 | |||||||
chr5:131697096 | T | G | 1 | a0001c0004t0001g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1202+1821A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697096 | |||||||
chr5:131697122 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+1795C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697122 | |||||||
chr5:131697191 | A | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0225 a0001c0001t0006g0300 others(1): Show |
4 | NA18965.hp2 NA18971.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+1726T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697191 | |||||||
chr5:131697261 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1202+1656G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697261 | |||||||
chr5:131697278 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1202+1639C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697278 | |||||||
chr5:131697390 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1202+1527T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697390 | |||||||
chr5:131697527 | G | A | 1 | a0002c0002t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1202+1390C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697527 | |||||||
chr5:131697605 | A | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202+1312T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697605 | |||||||
chr5:131697704 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1202+1213C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697704 | |||||||
chr5:131697801 | A | C | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1202+1116T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697801 | |||||||
chr5:131697910 | A | G | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1202+1007T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697910 | |||||||
chr5:131697932 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202+985C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697932 | |||||||
chr5:131697968 | C | CA | 19 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(16): Show |
19 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1202+948dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697968 | |||||||
chr5:131697968 | CA | C | 57 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0074 others(54): Show |
57 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1202+948delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697968 | |||||||
chr5:131697985 | A | G | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1202+932T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697985 | |||||||
chr5:131697989 | A | G | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1202+928T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131697989 | |||||||
chr5:131698140 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1202+777T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698140 | |||||||
chr5:131698207 | G | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1202+710C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698207 | |||||||
chr5:131698257 | A | C | 2 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+660T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698257 | |||||||
chr5:131698509 | G | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0049 |
3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1202+408C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 11/17 | chr5 | 131698509 | |||||||
chr5:131699052 | A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1117-50T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699052 | |||||||
chr5:131699395 | C | CT | 55 | a0001c0001t0001g0244 a0001c0001t0001g0290 a0001c0001t0003g0020 others(52): Show |
56 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1117-394dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699395 | |||||||
chr5:131699443 | G | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1117-441C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699443 | |||||||
chr5:131699522 | T | C | 1 | a0001c0001t0006g0297 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1117-520A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699522 | |||||||
chr5:131699721 | G | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1117-719C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699721 | |||||||
chr5:131699909 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1117-907T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699909 | |||||||
chr5:131699916 | C | CA | 7 | a0001c0001t0001g0174 a0001c0001t0002g0278 a0001c0001t0007g0302 others(4): Show |
7 | HG02451.hp1 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117-915dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699916 | C | CAA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0175 a0001c0001t0001g0178 others(6): Show |
9 | HG01993.hp1 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-916_1117-915d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699916 | C | CAAA | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(118): Show |
121 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1117-917_1117-915d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699916 | C | CAAAA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0001g0224 others(13): Show |
16 | HG00642.hp2 HG01175.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1117-918_1117-915d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699916 | CAAAAAAA others(3): Show |
C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-924_1117-915d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699916 | CAAAAAAA others(6): Show |
C | 37 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(34): Show |
37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1117-927_1117-915d others(15): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699916 | |||||||
chr5:131699983 | T | C | 3 | a0001c0001t0005g0115 a0002c0002t0002g0006 a0008c0011t0005g0121 |
3 | HG04115.hp2 NA18939.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1117-981A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699983 | |||||||
chr5:131699999 | T | C | 1 | a0006c0010t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1117-997A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131699999 | |||||||
chr5:131700280 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1117-1278G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700280 | |||||||
chr5:131700330 | T | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-1328A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700330 | |||||||
chr5:131700444 | G | A | 44 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(41): Show |
44 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1117-1442C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700444 | |||||||
chr5:131700458 | T | TA | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.1117-1457dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700458 | |||||||
chr5:131700506 | C | T | 1 | a0002c0002t0017g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1117-1504G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700506 | |||||||
chr5:131700545 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1117-1543G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700545 | |||||||
chr5:131700739 | T | TA | 13 | a0001c0001t0001g0175 a0002c0002t0018g0059 a0003c0003t0002g0311 others(10): Show |
13 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-1738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700739 | |||||||
chr5:131700823 | T | C | 10 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
10 | HG00408.hp2 HG02015.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-1821A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131700823 | |||||||
chr5:131701135 | T | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1117-2133A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701135 | |||||||
chr5:131701272 | T | G | 3 | a0001c0001t0008g0045 a0001c0001t0008g0046 a0001c0001t0008g0048 |
3 | HG01496.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1117-2270A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701272 | |||||||
chr5:131701544 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1116+2521C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701544 | |||||||
chr5:131701723 | C | T | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1116+2342G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701723 | |||||||
chr5:131701957 | C | CA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0002g0055 others(7): Show |
10 | HG01081.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1116+2107dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131701957 | |||||||
chr5:131702030 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+2035T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702030 | |||||||
chr5:131702066 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1116+1999A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702066 | |||||||
chr5:131702221 | T | C | 1 | a0002c0002t0002g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1116+1844A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702221 | |||||||
chr5:131702222 | G | A | 1 | a0002c0002t0002g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1116+1843C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702222 | |||||||
chr5:131702739 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1116+1326C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702739 | |||||||
chr5:131702824 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1116+1241G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702824 | |||||||
chr5:131702938 | T | C | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1116+1127A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131702938 | |||||||
chr5:131703058 | T | G | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1116+1007A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703058 | |||||||
chr5:131703231 | C | T | 1 | a0001c0001t0011g0308 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1116+834G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703231 | |||||||
chr5:131703247 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1116+818T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703247 | |||||||
chr5:131703399 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1116+666G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703399 | |||||||
chr5:131703418 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1116+647A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703418 | |||||||
chr5:131703498 | A | G | 5 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0002t0002g0146 others(2): Show |
5 | HG01261.hp2 HG01433.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+567T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703498 | |||||||
chr5:131703673 | T | C | 13 | a0002c0002t0004g0001 a0002c0002t0004g0053 a0002c0002t0004g0128 others(10): Show |
14 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116+392A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703673 | |||||||
chr5:131703707 | C | T | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+358G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703707 | |||||||
chr5:131703714 | C | T | 3 | a0002c0002t0002g0160 a0002c0002t0002g0161 a0002c0002t0002g0282 |
3 | HG01255.hp1 HG01516.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1116+351G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703714 | |||||||
chr5:131703715 | G | A | 2 | a0006c0010t0001g0205 a0006c0010t0001g0292 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1116+350C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703715 | |||||||
chr5:131703893 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1116+172A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703893 | |||||||
chr5:131703935 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1116+130T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703935 | |||||||
chr5:131703940 | C | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1116+125G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 10/17 | chr5 | 131703940 | |||||||
chr5:131704612 | T | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0054 a0001c0001t0002g0076 others(6): Show |
9 | HG02135.hp2 HG02165.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.915-346A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704612 | |||||||
chr5:131704812 | C | T | 1 | a0004c0007t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.915-546G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704812 | |||||||
chr5:131704859 | C | T | 99 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(96): Show |
99 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.915-593G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131704859 | |||||||
chr5:131705177 | A | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.915-911T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705177 | |||||||
chr5:131705184 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.915-918C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705184 | |||||||
chr5:131705196 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.915-930A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705196 | |||||||
chr5:131705294 | C | T | 2 | a0004c0007t0001g0183 a0004c0007t0001g0184 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.915-1028G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705294 | |||||||
chr5:131705380 | G | A | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.914+1031C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705380 | |||||||
chr5:131705383 | G | C | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.914+1028C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705383 | |||||||
chr5:131705502 | C | G | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.914+909G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705502 | |||||||
chr5:131705553 | C | T | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+858G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705553 | |||||||
chr5:131705681 | C | T | 1 | a0001c0001t0005g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.914+730G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705681 | |||||||
chr5:131705782 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.914+629C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705782 | |||||||
chr5:131705897 | C | T | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(197): Show |
200 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.914+514G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705897 | |||||||
chr5:131705970 | T | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.914+441A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131705970 | |||||||
chr5:131706031 | G | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.914+380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 9/17 | chr5 | 131706031 | |||||||
chr5:131706618 | A | C | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.779-72T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706618 | |||||||
chr5:131706725 | A | G | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.779-179T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706725 | |||||||
chr5:131706760 | A | G | 1 | a0002c0002t0002g0006 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.779-214T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131706760 | |||||||
chr5:131707174 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.779-628C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707174 | |||||||
chr5:131707278 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.779-732G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707278 | |||||||
chr5:131707296 | A | G | 2 | a0002c0002t0002g0163 a0002c0002t0002g0273 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.779-750T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707296 | |||||||
chr5:131707513 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-967A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707513 | |||||||
chr5:131707784 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.779-1238T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707784 | |||||||
chr5:131707966 | T | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.778+1235A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707966 | |||||||
chr5:131707967 | T | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.778+1234A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131707967 | |||||||
chr5:131708186 | G | C | 6 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.778+1015C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708186 | |||||||
chr5:131708210 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.778+991A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708210 | |||||||
chr5:131708395 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0211 others(8): Show |
11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.778+806G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708395 | |||||||
chr5:131708441 | A | G | 4 | a0001c0001t0001g0303 a0004c0007t0001g0176 a0004c0007t0001g0183 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+760T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708441 | |||||||
chr5:131708789 | G | GA | 6 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0002g0083 others(3): Show |
6 | HG01081.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+411dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708789 | |||||||
chr5:131708858 | T | C | 17 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(14): Show |
17 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.778+343A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708858 | |||||||
chr5:131708898 | G | GT | 41 | a0001c0001t0001g0064 a0001c0001t0001g0165 a0001c0001t0003g0020 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.778+302dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708898 | |||||||
chr5:131708899 | T | G | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.778+302A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131708899 | |||||||
chr5:131709048 | T | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.778+153A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131709048 | |||||||
chr5:131709150 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.778+51G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 8/17 | chr5 | 131709150 | |||||||
chr5:131709390 | C | A | 2 | a0001c0001t0001g0255 a0001c0001t0006g0297 |
2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.707-118G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709390 | |||||||
chr5:131709575 | A | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-303T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709575 | |||||||
chr5:131709699 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01099.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.707-427T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709699 | |||||||
chr5:131709825 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.707-553T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709825 | |||||||
chr5:131709849 | G | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-577C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131709849 | |||||||
chr5:131710078 | T | G | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.706+500A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710078 | |||||||
chr5:131710142 | T | C | 204 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(201): Show |
204 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.706+436A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710142 | |||||||
chr5:131710337 | C | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+241G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710337 | |||||||
chr5:131710496 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.706+82T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710496 | |||||||
chr5:131710535 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.706+43A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 7/17 | chr5 | 131710535 | |||||||
chr5:131710696 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.623-35C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710696 | |||||||
chr5:131710720 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0156 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.623-59C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710720 | |||||||
chr5:131710994 | A | G | 2 | a0002c0002t0004g0143 a0002c0002t0004g0284 |
2 | HG02056.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.623-333T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131710994 | |||||||
chr5:131711015 | T | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.623-354A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711015 | |||||||
chr5:131711052 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.623-391C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711052 | |||||||
chr5:131711107 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.623-446T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711107 | |||||||
chr5:131711185 | A | G | 2 | a0002c0002t0002g0289 a0002c0002t0005g0127 |
2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.623-524T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711185 | |||||||
chr5:131711264 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.623-603C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711264 | |||||||
chr5:131711370 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0155 |
2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.623-709G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711370 | |||||||
chr5:131711404 | T | C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.623-743A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711404 | |||||||
chr5:131711890 | T | C | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.623-1229A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711890 | |||||||
chr5:131711928 | G | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.623-1267C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711928 | |||||||
chr5:131711943 | A | G | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.623-1282T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131711943 | |||||||
chr5:131712359 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0007g0302 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.623-1698A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712359 | |||||||
chr5:131712408 | G | A | 3 | a0002c0002t0002g0160 a0002c0002t0002g0161 a0002c0002t0002g0282 |
3 | HG01255.hp1 HG01516.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.623-1747C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712408 | |||||||
chr5:131712429 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.623-1768C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712429 | |||||||
chr5:131712557 | C | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.623-1896G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712557 | |||||||
chr5:131712596 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-1935A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712596 | |||||||
chr5:131712631 | A | G | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.623-1970T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131712631 | |||||||
chr5:131713050 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0178 a0001c0001t0001g0182 others(1): Show |
4 | NA18955.hp2 NA18956.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.623-2389G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713050 | |||||||
chr5:131713200 | C | G | 1 | a0001c0001t0005g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.623-2539G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713200 | |||||||
chr5:131713341 | C | T | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.623-2680G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713341 | |||||||
chr5:131713538 | A | C | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.623-2877T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713538 | |||||||
chr5:131713589 | TAAC | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.623-2931_623-2929d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713589 | |||||||
chr5:131713644 | T | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622+2921A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713644 | |||||||
chr5:131713703 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.622+2862T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713703 | |||||||
chr5:131713720 | C | T | 1 | a0002c0002t0002g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.622+2845G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713720 | |||||||
chr5:131713785 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.622+2780G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713785 | |||||||
chr5:131713876 | G | C | 14 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0085 others(11): Show |
14 | NA18945.hp1 NA18947.hp2 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.622+2689C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713876 | |||||||
chr5:131713884 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.622+2681A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713884 | |||||||
chr5:131713890 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0006g0297 |
2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.622+2675A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713890 | |||||||
chr5:131713892 | T | G | 184 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(181): Show |
184 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.622+2673A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131713892 | |||||||
chr5:131714009 | C | T | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.622+2556G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714009 | |||||||
chr5:131714244 | T | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.622+2321A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714244 | |||||||
chr5:131714264 | A | G | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.622+2301T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714264 | |||||||
chr5:131714292 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.622+2273A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714292 | |||||||
chr5:131714417 | A | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.622+2148T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714417 | |||||||
chr5:131714517 | A | C | 1 | a0001c0004t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.622+2048T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714517 | |||||||
chr5:131714572 | C | T | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.622+1993G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714572 | |||||||
chr5:131714652 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622+1913G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714652 | |||||||
chr5:131714658 | A | C | 1 | a0001c0001t0005g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.622+1907T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714658 | |||||||
chr5:131714663 | T | C | 1 | a0002c0002t0004g0144 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.622+1902A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131714663 | |||||||
chr5:131715087 | T | G | 43 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0074 others(40): Show |
43 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.622+1478A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715087 | |||||||
chr5:131715221 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622+1344G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715221 | |||||||
chr5:131715322 | T | C | 200 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(197): Show |
200 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.622+1243A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715322 | |||||||
chr5:131715343 | G | A | 4 | a0001c0001t0003g0031 a0001c0001t0003g0036 a0001c0001t0003g0040 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.622+1222C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715343 | |||||||
chr5:131715511 | C | A | 2 | a0002c0002t0004g0007 a0002c0002t0004g0162 |
2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.622+1054G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715511 | |||||||
chr5:131715635 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.622+930T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715635 | |||||||
chr5:131715714 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.622+851G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715714 | |||||||
chr5:131715965 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.622+600C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715965 | |||||||
chr5:131715985 | T | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.622+580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131715985 | |||||||
chr5:131716018 | A | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0122 |
2 | NA19080.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.622+547T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716018 | |||||||
chr5:131716223 | T | G | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.622+342A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716223 | |||||||
chr5:131716286 | A | C | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.622+279T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716286 | |||||||
chr5:131716386 | G | A | 1 | a0001c0004t0001g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.622+179C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716386 | |||||||
chr5:131716399 | T | A | 1 | a0001c0001t0008g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622+166A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 6/17 | chr5 | 131716399 | |||||||
chr5:131716749 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.531-93G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716749 | |||||||
chr5:131716868 | T | C | 1 | a0001c0001t0009g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.531-212A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716868 | |||||||
chr5:131716977 | A | T | 1 | a0001c0001t0005g0050 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.531-321T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716977 | |||||||
chr5:131716979 | T | A | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-323A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716979 | |||||||
chr5:131716990 | T | A | 206 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(203): Show |
206 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.531-334A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716990 | |||||||
chr5:131716992 | T | A | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.531-336A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131716992 | |||||||
chr5:131717036 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717036 | |||||||
chr5:131717151 | C | T | 4 | a0002c0002t0002g0082 a0002c0002t0002g0141 a0002c0002t0002g0289 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-495G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717151 | |||||||
chr5:131717294 | A | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.531-638T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717294 | |||||||
chr5:131717359 | C | T | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.531-703G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717359 | |||||||
chr5:131717530 | A | G | 1 | a0001c0001t0007g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.531-874T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717530 | |||||||
chr5:131717720 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.531-1064C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131717720 | |||||||
chr5:131718027 | C | CA | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.530+958dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718027 | |||||||
chr5:131718027 | CA | C | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.530+958delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718027 | |||||||
chr5:131718047 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.530+939G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718047 | |||||||
chr5:131718048 | C | T | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.530+938G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718048 | |||||||
chr5:131718064 | C | T | 1 | a0002c0002t0004g0144 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.530+922G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718064 | |||||||
chr5:131718065 | G | A | 1 | a0001c0001t0006g0258 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.530+921C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718065 | |||||||
chr5:131718077 | A | G | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.530+909T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718077 | |||||||
chr5:131718106 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.530+880G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718106 | |||||||
chr5:131718107 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.530+879C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718107 | |||||||
chr5:131718163 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.530+823C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718163 | |||||||
chr5:131718187 | T | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.530+799A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718187 | |||||||
chr5:131718641 | G | A | 2 | a0001c0001t0003g0028 a0001c0013t0003g0027 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.530+345C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718641 | |||||||
chr5:131718691 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.530+295G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 5/17 | chr5 | 131718691 | |||||||
chr5:131719150 | G | A | 1 | a0001c0004t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.456-90C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 4/17 | chr5 | 131719150 | |||||||
chr5:131719429 | C | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.355-12G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719429 | |||||||
chr5:131719545 | C | T | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.355-128G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719545 | |||||||
chr5:131719853 | T | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.355-436A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719853 | |||||||
chr5:131719918 | T | C | 1 | a0002c0002t0002g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.355-501A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131719918 | |||||||
chr5:131720018 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.355-601G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720018 | |||||||
chr5:131720293 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.355-876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720293 | |||||||
chr5:131720527 | A | G | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.355-1110T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720527 | |||||||
chr5:131720740 | T | C | 1 | a0001c0001t0006g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.355-1323A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720740 | |||||||
chr5:131720975 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.355-1558A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131720975 | |||||||
chr5:131721004 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.355-1587C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721004 | |||||||
chr5:131721116 | T | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.355-1699A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721116 | |||||||
chr5:131721175 | C | T | 1 | a0002c0002t0004g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.355-1758G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721175 | |||||||
chr5:131721271 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0271 |
2 | NA18959.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.355-1854A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721271 | |||||||
chr5:131721274 | G | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-1857C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721274 | |||||||
chr5:131721333 | G | A | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.355-1916C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721333 | |||||||
chr5:131721337 | T | G | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.355-1920A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721337 | |||||||
chr5:131721416 | T | A | 1 | a0006c0010t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-1999A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721416 | |||||||
chr5:131721525 | G | A | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.355-2108C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721525 | |||||||
chr5:131721569 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.355-2152G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721569 | |||||||
chr5:131721689 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.355-2272C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721689 | |||||||
chr5:131721690 | C | T | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.355-2273G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721690 | |||||||
chr5:131721697 | C | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(14): Show |
17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-2280G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131721697 | |||||||
chr5:131722006 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.355-2589C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722006 | |||||||
chr5:131722206 | A | T | 1 | a0002c0002t0002g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-2789T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722206 | |||||||
chr5:131722243 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355-2826T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722243 | |||||||
chr5:131722337 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0155 |
2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.355-2920G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722337 | |||||||
chr5:131722338 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.355-2921C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722338 | |||||||
chr5:131722384 | C | G | 1 | a0006c0010t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.355-2967G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722384 | |||||||
chr5:131722645 | C | T | 46 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(43): Show |
46 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.355-3228G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722645 | |||||||
chr5:131722674 | C | T | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.355-3257G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722674 | |||||||
chr5:131722883 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.355-3466T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131722883 | |||||||
chr5:131723053 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.355-3636A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723053 | |||||||
chr5:131723073 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.355-3656T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723073 | |||||||
chr5:131723093 | A | C | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.355-3676T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723093 | |||||||
chr5:131723379 | A | T | 1 | a0001c0001t0006g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.355-3962T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723379 | |||||||
chr5:131723429 | G | A | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.355-4012C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723429 | |||||||
chr5:131723483 | A | G | 2 | a0001c0001t0002g0081 a0001c0001t0005g0080 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.355-4066T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723483 | |||||||
chr5:131723619 | T | G | 37 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(34): Show |
37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.355-4202A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723619 | |||||||
chr5:131723709 | A | T | 1 | a0001c0001t0005g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.355-4292T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131723709 | |||||||
chr5:131724099 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.355-4682G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724099 | |||||||
chr5:131724215 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-4798C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724215 | |||||||
chr5:131724419 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.355-5002G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724419 | |||||||
chr5:131724629 | CAA | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0322 |
3 | HG00738.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.355-5214_355-5213d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724629 | |||||||
chr5:131724769 | TTTGCCTA others(20): Show |
T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0290 |
3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.355-5379_355-5353d others(29): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724769 | |||||||
chr5:131724799 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.355-5382C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724799 | |||||||
chr5:131724841 | G | A | 1 | a0002c0002t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.355-5424C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131724841 | |||||||
chr5:131725063 | T | G | 37 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(34): Show |
37 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.355-5646A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725063 | |||||||
chr5:131725140 | C | A | 1 | a0001c0004t0001g0062 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.355-5723G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725140 | |||||||
chr5:131725418 | A | C | 277 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(274): Show |
278 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(275): Show |
intron_variant | MODIFIER | c.354+5486T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725418 | |||||||
chr5:131725746 | G | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.354+5158C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725746 | |||||||
chr5:131725800 | G | A | 1 | a0001c0013t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.354+5104C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725800 | |||||||
chr5:131725811 | C | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.354+5093G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725811 | |||||||
chr5:131725914 | T | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.354+4990A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725914 | |||||||
chr5:131725987 | G | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+4917C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131725987 | |||||||
chr5:131726133 | A | G | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+4771T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726133 | |||||||
chr5:131726343 | C | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.354+4561G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726343 | |||||||
chr5:131726714 | T | C | 17 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0187 others(14): Show |
17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+4190A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726714 | |||||||
chr5:131726889 | C | T | 2 | a0001c0008t0002g0111 a0001c0008t0002g0286 |
2 | NA18940.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.354+4015G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726889 | |||||||
chr5:131726949 | T | C | 4 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+3955A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131726949 | |||||||
chr5:131727356 | C | A | 1 | a0001c0001t0006g0258 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.354+3548G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727356 | |||||||
chr5:131727380 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.354+3524G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727380 | |||||||
chr5:131727386 | C | A | 2 | a0002c0002t0004g0132 a0002c0002t0004g0288 |
2 | NA18978.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.354+3518G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727386 | |||||||
chr5:131727660 | G | A | 11 | a0001c0001t0001g0056 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.354+3244C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727660 | |||||||
chr5:131727676 | T | C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+3228A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131727676 | |||||||
chr5:131728000 | T | C | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.354+2904A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728000 | |||||||
chr5:131728041 | G | A | 5 | a0001c0001t0007g0060 a0001c0001t0007g0302 a0001c0001t0007g0323 others(2): Show |
5 | HG02630.hp1 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+2863C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728041 | |||||||
chr5:131728143 | C | T | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.354+2761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728143 | |||||||
chr5:131728289 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.354+2615A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728289 | |||||||
chr5:131728725 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+2179G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728725 | |||||||
chr5:131728882 | T | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0190 a0001c0001t0001g0218 others(2): Show |
5 | HG00733.hp1 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+2022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728882 | |||||||
chr5:131728943 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.354+1961G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131728943 | |||||||
chr5:131729092 | G | A | 1 | a0002c0002t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.354+1812C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729092 | |||||||
chr5:131729144 | G | T | 5 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0107 others(2): Show |
5 | NA18949.hp1 NA18951.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+1760C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729144 | |||||||
chr5:131729157 | G | C | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.354+1747C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729157 | |||||||
chr5:131729194 | T | A | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.354+1710A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729194 | |||||||
chr5:131729249 | G | A | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.354+1655C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729249 | |||||||
chr5:131729291 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.354+1613G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729291 | |||||||
chr5:131729862 | C | T | 2 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+1042G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131729862 | |||||||
chr5:131730229 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.354+675G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730229 | |||||||
chr5:131730411 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.354+493C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730411 | |||||||
chr5:131730640 | AAG | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.354+262_354+263del others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730640 | |||||||
chr5:131730884 | A | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.354+20T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 3/17 | chr5 | 131730884 | |||||||
chr5:131731160 | T | A | 7 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-122A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731160 | |||||||
chr5:131731206 | C | A | 6 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-168G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731206 | |||||||
chr5:131731300 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.220-262C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731300 | |||||||
chr5:131731641 | C | CA | 41 | a0001c0001t0002g0098 a0001c0001t0002g0124 a0001c0001t0003g0020 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.220-604dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731641 | |||||||
chr5:131731653 | C | A | 1 | a0001c0005t0006g0071 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.220-615G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731653 | |||||||
chr5:131731851 | T | TA | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-814dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731851 | |||||||
chr5:131731970 | T | G | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-932A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131731970 | |||||||
chr5:131732166 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-1128A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732166 | |||||||
chr5:131732245 | C | A | 1 | a0001c0012t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-1207G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732245 | |||||||
chr5:131732402 | C | G | 99 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(96): Show |
99 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.220-1364G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732402 | |||||||
chr5:131732553 | G | C | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(31): Show |
34 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.220-1515C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732553 | |||||||
chr5:131732554 | C | T | 4 | a0002c0002t0004g0129 a0002c0002t0004g0140 a0002c0002t0004g0157 others(1): Show |
4 | NA18962.hp2 NA18984.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-1516G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732554 | |||||||
chr5:131732669 | T | G | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1631A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732669 | |||||||
chr5:131732670 | T | C | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1632A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732670 | |||||||
chr5:131732671 | A | T | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1633T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732671 | |||||||
chr5:131732716 | G | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-1678C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732716 | |||||||
chr5:131732807 | T | G | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-1769A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131732807 | |||||||
chr5:131733102 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-2064C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733102 | |||||||
chr5:131733150 | G | A | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-2112C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733150 | |||||||
chr5:131733168 | C | T | 1 | a0001c0001t0005g0116 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.220-2130G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733168 | |||||||
chr5:131733277 | G | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-2239C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733277 | |||||||
chr5:131733349 | C | G | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-2311G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733349 | |||||||
chr5:131733371 | T | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.220-2333A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733371 | |||||||
chr5:131733500 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2462G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733500 | |||||||
chr5:131733502 | C | T | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220-2464G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733502 | |||||||
chr5:131733506 | G | A | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.220-2468C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733506 | |||||||
chr5:131733645 | A | G | 1 | a0001c0001t0009g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.220-2607T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733645 | |||||||
chr5:131733759 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2721T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733759 | |||||||
chr5:131733771 | G | A | 1 | a0001c0001t0008g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.220-2733C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733771 | |||||||
chr5:131733786 | T | C | 1 | a0002c0002t0002g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.220-2748A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733786 | |||||||
chr5:131733850 | A | T | 1 | a0001c0001t0002g0124 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.220-2812T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131733850 | |||||||
chr5:131734115 | G | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-3077C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734115 | |||||||
chr5:131734159 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.220-3121G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734159 | |||||||
chr5:131734320 | T | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-3282A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734320 | |||||||
chr5:131734337 | CTGA | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-3302_220-3300d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734337 | |||||||
chr5:131734409 | TC | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-3372delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734409 | |||||||
chr5:131734484 | T | C | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.220-3446A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734484 | |||||||
chr5:131734544 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.220-3506A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734544 | |||||||
chr5:131734593 | A | T | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3555T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734593 | |||||||
chr5:131734627 | C | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.220-3589G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734627 | |||||||
chr5:131734630 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-3592G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734630 | |||||||
chr5:131734657 | G | A | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3619C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734657 | |||||||
chr5:131734786 | G | A | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220-3748C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131734786 | |||||||
chr5:131735009 | C | T | 10 | a0001c0001t0007g0060 a0001c0001t0007g0302 a0001c0001t0007g0323 others(7): Show |
10 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-3971G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735009 | |||||||
chr5:131735165 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.220-4127G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735165 | |||||||
chr5:131735210 | C | CA | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-4173dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735210 | |||||||
chr5:131735259 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.220-4221A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735259 | |||||||
chr5:131735284 | G | A | 2 | a0002c0002t0004g0157 a0002c0002t0004g0164 |
2 | NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.220-4246C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735284 | |||||||
chr5:131735324 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-4286C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735324 | |||||||
chr5:131735404 | G | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.220-4366C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735404 | |||||||
chr5:131735454 | A | ATTTTATA others(7): Show |
1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-4417_220-4416i others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735454 | |||||||
chr5:131735474 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-4436A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735474 | |||||||
chr5:131735494 | C | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-4456G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735494 | |||||||
chr5:131735502 | A | G | 1 | a0006c0010t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-4464T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735502 | |||||||
chr5:131735553 | C | G | 150 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.220-4515G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735553 | |||||||
chr5:131735588 | G | A | 1 | a0001c0005t0006g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.220-4550C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735588 | |||||||
chr5:131735612 | A | T | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.220-4574T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735612 | |||||||
chr5:131735625 | TGTATACG others(7): Show |
T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-4601_220-4588d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735625 | |||||||
chr5:131735640 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-4602C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735640 | |||||||
chr5:131735747 | A | T | 99 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0056 others(96): Show |
99 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.220-4709T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735747 | |||||||
chr5:131735787 | A | C | 4 | a0002c0002t0004g0129 a0002c0002t0004g0140 a0002c0002t0004g0157 others(1): Show |
4 | NA18962.hp2 NA18984.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-4749T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735787 | |||||||
chr5:131735807 | A | ATG | 7 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0001t0003g0038 others(4): Show |
7 | HG00642.hp1 HG01496.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-4771_220-4770d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735807 | |||||||
chr5:131735807 | ATG | A | 14 | a0001c0001t0002g0055 a0001c0001t0003g0020 a0001c0001t0007g0302 others(11): Show |
14 | HG01081.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-4771_220-4770d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735807 | |||||||
chr5:131735825 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.220-4787C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735825 | |||||||
chr5:131735929 | C | G | 4 | a0002c0002t0002g0125 a0002c0002t0002g0163 a0002c0002t0002g0273 others(1): Show |
4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4891G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131735929 | |||||||
chr5:131736474 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.220-5436C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736474 | |||||||
chr5:131736717 | C | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.220-5679G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736717 | |||||||
chr5:131736804 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0185 |
2 | NA18956.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.220-5766G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736804 | |||||||
chr5:131736846 | T | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.220-5808A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736846 | |||||||
chr5:131736869 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.220-5831G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736869 | |||||||
chr5:131736916 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.220-5878C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736916 | |||||||
chr5:131736929 | A | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.220-5891T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736929 | |||||||
chr5:131736988 | A | C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-5950T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131736988 | |||||||
chr5:131737056 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-6018C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737056 | |||||||
chr5:131737220 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-6182G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737220 | |||||||
chr5:131737258 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0279 |
3 | HG01109.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.220-6220G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737258 | |||||||
chr5:131737345 | T | A | 1 | a0001c0001t0005g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.220-6307A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737345 | |||||||
chr5:131737672 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-6634G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737672 | |||||||
chr5:131737712 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-6674G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737712 | |||||||
chr5:131737786 | T | TA | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-6749_220-6748i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131737786 | |||||||
chr5:131738309 | G | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0122 |
2 | NA19080.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.219+6255C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738309 | |||||||
chr5:131738483 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+6081A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738483 | |||||||
chr5:131738504 | C | A | 21 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0006 others(18): Show |
21 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+6060G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738504 | |||||||
chr5:131738610 | G | A | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.219+5954C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738610 | |||||||
chr5:131738658 | C | G | 1 | a0001c0001t0001g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+5906G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738658 | |||||||
chr5:131738660 | C | T | 1 | a0003c0003t0002g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+5904G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738660 | |||||||
chr5:131738812 | CT | C | 59 | a0001c0001t0002g0055 a0001c0001t0002g0093 a0001c0001t0003g0020 others(56): Show |
59 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.219+5751delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131738812 | |||||||
chr5:131739008 | G | T | 1 | a0001c0001t0002g0084 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.219+5556C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739008 | |||||||
chr5:131739289 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.219+5275G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739289 | |||||||
chr5:131739326 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+5238G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739326 | |||||||
chr5:131739327 | G | A | 1 | a0002c0006t0004g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.219+5237C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739327 | |||||||
chr5:131739356 | T | C | 1 | a0001c0001t0022g0208 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.219+5208A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739356 | |||||||
chr5:131739477 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+5087G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739477 | |||||||
chr5:131739579 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4985G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739579 | |||||||
chr5:131739760 | C | G | 3 | a0001c0001t0007g0060 a0001c0001t0007g0323 a0001c0001t0007g0324 |
3 | HG02630.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.219+4804G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739760 | |||||||
chr5:131739769 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4795G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739769 | |||||||
chr5:131739773 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219+4791C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739773 | |||||||
chr5:131739812 | C | CA | 41 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0179 others(38): Show |
41 | HG00438.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.219+4751dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | |||||||
chr5:131739812 | CA | C | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0055 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.219+4751delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | |||||||
chr5:131739812 | CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+4741_219+4751d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739812 | |||||||
chr5:131739824 | A | C | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219+4740T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739824 | |||||||
chr5:131739832 | A | AC | 4 | a0001c0001t0003g0035 a0001c0001t0003g0039 a0001c0001t0003g0049 others(1): Show |
4 | HG00642.hp1 HG01071.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+4731_219+4732i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739832 | |||||||
chr5:131739832 | A | C | 26 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(23): Show |
26 | HG00639.hp1 HG01069.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.219+4732T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739832 | |||||||
chr5:131739833 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0202 |
2 | NA18979.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.219+4731T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739833 | |||||||
chr5:131739835 | A | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0220 a0001c0001t0001g0261 others(2): Show |
5 | HG01934.hp1 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+4729T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739835 | |||||||
chr5:131739837 | A | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+4727T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739837 | |||||||
chr5:131739934 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.219+4630A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131739934 | |||||||
chr5:131740165 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.219+4399G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740165 | |||||||
chr5:131740228 | C | T | 276 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(273): Show |
277 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.219+4336G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740228 | |||||||
chr5:131740374 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+4190T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740374 | |||||||
chr5:131740496 | G | C | 1 | a0001c0001t0002g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219+4068C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740496 | |||||||
chr5:131740531 | T | A | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.219+4033A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740531 | |||||||
chr5:131740577 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219+3987C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740577 | |||||||
chr5:131740983 | T | TA | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+3580dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131740983 | |||||||
chr5:131741173 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+3391T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741173 | |||||||
chr5:131741498 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.219+3066A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741498 | |||||||
chr5:131741635 | T | C | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+2929A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741635 | |||||||
chr5:131741827 | C | T | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219+2737G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741827 | |||||||
chr5:131741869 | C | T | 7 | a0001c0001t0003g0304 a0001c0001t0003g0305 a0001c0001t0003g0306 others(4): Show |
7 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+2695G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131741869 | |||||||
chr5:131742016 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.219+2548G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742016 | |||||||
chr5:131742212 | C | A | 19 | a0001c0001t0002g0113 a0001c0001t0002g0124 a0001c0001t0002g0154 others(16): Show |
19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+2352G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742212 | |||||||
chr5:131742273 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.219+2291C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742273 | |||||||
chr5:131742335 | A | G | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.219+2229T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742335 | |||||||
chr5:131742340 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.219+2224A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742340 | |||||||
chr5:131742441 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.219+2123G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742441 | |||||||
chr5:131742637 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+1927G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742637 | |||||||
chr5:131742645 | T | C | 3 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0319 |
3 | HG01884.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.219+1919A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742645 | |||||||
chr5:131742805 | C | G | 150 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
150 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.219+1759G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742805 | |||||||
chr5:131742993 | G | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0049 |
3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219+1571C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131742993 | |||||||
chr5:131743046 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+1518C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743046 | |||||||
chr5:131743062 | T | C | 2 | a0001c0001t0002g0151 a0001c0001t0002g0153 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.219+1502A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743062 | |||||||
chr5:131743328 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+1236G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743328 | |||||||
chr5:131743595 | T | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.219+969A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743595 | |||||||
chr5:131743614 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+950G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743614 | |||||||
chr5:131743863 | G | T | 2 | a0006c0010t0001g0205 a0006c0010t0001g0292 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.219+701C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743863 | |||||||
chr5:131743888 | C | G | 1 | a0001c0001t0006g0241 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.219+676G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131743888 | |||||||
chr5:131744036 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.219+528C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131744036 | |||||||
chr5:131744115 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.219+449G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 2/17 | chr5 | 131744115 | |||||||
chr5:131744808 | A | AAT | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-120_93-119dupAT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744808 | |||||||
chr5:131744913 | C | G | 1 | a0002c0002t0002g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.93-223G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744913 | |||||||
chr5:131744993 | T | C | 1 | a0002c0002t0004g0135 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.93-303A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131744993 | |||||||
chr5:131745074 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.93-384G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745074 | |||||||
chr5:131745267 | C | T | 17 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0187 others(14): Show |
17 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.93-577G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745267 | |||||||
chr5:131745288 | G | A | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93-598C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745288 | |||||||
chr5:131745436 | C | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-746G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745436 | |||||||
chr5:131745460 | T | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-770A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745460 | |||||||
chr5:131745577 | T | A | 1 | a0006c0010t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.93-887A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745577 | |||||||
chr5:131745591 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.93-901A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745591 | |||||||
chr5:131745620 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-930A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745620 | |||||||
chr5:131745673 | G | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0049 |
3 | HG00642.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.93-983C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745673 | |||||||
chr5:131745695 | A | C | 1 | a0004c0007t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.93-1005T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745695 | |||||||
chr5:131745761 | T | A | 1 | a0001c0001t0003g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.93-1071A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745761 | |||||||
chr5:131745833 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93-1143G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745833 | |||||||
chr5:131745961 | T | G | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-1271A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131745961 | |||||||
chr5:131746203 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-1513C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746203 | |||||||
chr5:131746384 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.93-1694T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746384 | |||||||
chr5:131746419 | C | T | 1 | a0001c0001t0005g0115 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.93-1729G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746419 | |||||||
chr5:131746520 | T | C | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-1830A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746520 | |||||||
chr5:131746962 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-2272A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746962 | |||||||
chr5:131746994 | A | G | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.93-2304T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131746994 | |||||||
chr5:131747393 | A | G | 1 | a0001c0001t0005g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.93-2703T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747393 | |||||||
chr5:131747585 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-2895G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747585 | |||||||
chr5:131747886 | A | G | 1 | a0002c0002t0002g0150 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.93-3196T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747886 | |||||||
chr5:131747889 | G | A | 1 | a0002c0002t0002g0150 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.93-3199C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131747889 | |||||||
chr5:131748136 | T | C | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.93-3446A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748136 | |||||||
chr5:131748173 | T | C | 9 | a0002c0002t0004g0001 a0002c0002t0004g0128 a0002c0002t0004g0137 others(6): Show |
10 | HG00408.hp1 HG01978.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-3483A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748173 | |||||||
chr5:131748453 | G | C | 1 | a0001c0005t0006g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93-3763C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748453 | |||||||
chr5:131748479 | G | A | 1 | a0002c0002t0002g0289 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.93-3789C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748479 | |||||||
chr5:131748549 | T | C | 1 | a0001c0001t0009g0170 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.93-3859A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748549 | |||||||
chr5:131748566 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.93-3876T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748566 | |||||||
chr5:131748630 | G | C | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-3940C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748630 | |||||||
chr5:131748691 | T | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-4001A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748691 | |||||||
chr5:131748696 | C | CA | 181 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(178): Show |
181 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.93-4007dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748696 | |||||||
chr5:131748709 | G | A | 10 | a0001c0001t0001g0165 a0001c0001t0003g0020 a0001c0001t0003g0038 others(7): Show |
10 | HG00642.hp1 HG02258.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-4019C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748709 | |||||||
chr5:131748709 | GA | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-4020delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748709 | |||||||
chr5:131748710 | A | G | 8 | a0001c0001t0003g0020 a0001c0001t0003g0038 a0001c0001t0003g0041 others(5): Show |
8 | HG00642.hp1 HG02258.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-4020T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748710 | |||||||
chr5:131748752 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-4062A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748752 | |||||||
chr5:131748786 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-4096G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748786 | |||||||
chr5:131748935 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-4245A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131748935 | |||||||
chr5:131749065 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.93-4375A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749065 | |||||||
chr5:131749233 | C | G | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-4543G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749233 | |||||||
chr5:131749293 | T | G | 1 | a0001c0001t0002g0278 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.93-4603A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749293 | |||||||
chr5:131749309 | G | A | 1 | a0001c0001t0003g0305 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.93-4619C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749309 | |||||||
chr5:131749621 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.93-4931T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131749621 | |||||||
chr5:131750051 | T | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-5361A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750051 | |||||||
chr5:131750057 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.93-5367C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750057 | |||||||
chr5:131750286 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.93-5596T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750286 | |||||||
chr5:131750288 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93-5598C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750288 | |||||||
chr5:131750492 | T | C | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.93-5802A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750492 | |||||||
chr5:131750616 | C | CT | 24 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0085 others(21): Show |
24 | HG01496.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.93-5927dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | |||||||
chr5:131750616 | C | CTT | 31 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.93-5928_93-5927dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | |||||||
chr5:131750616 | CT | C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0294 others(3): Show |
6 | HG01069.hp1 HG01168.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-5927delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750616 | |||||||
chr5:131750638 | A | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-5948T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750638 | |||||||
chr5:131750882 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6192G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750882 | |||||||
chr5:131750924 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(14): Show |
17 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.93-6234T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750924 | |||||||
chr5:131750955 | T | C | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.93-6265A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131750955 | |||||||
chr5:131751078 | G | C | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.93-6388C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751078 | |||||||
chr5:131751129 | C | A | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-6439G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751129 | |||||||
chr5:131751187 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-6497T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751187 | |||||||
chr5:131751244 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-6554G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751244 | |||||||
chr5:131751251 | A | C | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-6561T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751251 | |||||||
chr5:131751341 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-6651G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751341 | |||||||
chr5:131751487 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-6797C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751487 | |||||||
chr5:131751571 | G | GA | 7 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
8 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6882dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751571 | |||||||
chr5:131751571 | GA | G | 8 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0007g0302 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-6882delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751571 | |||||||
chr5:131751703 | T | C | 1 | a0001c0001t0007g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.93-7013A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751703 | |||||||
chr5:131751762 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.93-7072C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751762 | |||||||
chr5:131751921 | C | G | 1 | a0001c0001t0003g0031 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.93-7231G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751921 | |||||||
chr5:131751953 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-7263A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751953 | |||||||
chr5:131751963 | T | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.93-7273A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131751963 | |||||||
chr5:131752037 | G | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-7347C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752037 | |||||||
chr5:131752101 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0020g0232 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.93-7411A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752101 | |||||||
chr5:131752174 | G | T | 1 | a0001c0001t0002g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.93-7484C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752174 | |||||||
chr5:131752538 | T | TA | 153 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
153 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.93-7849dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752538 | |||||||
chr5:131752538 | T | TAA | 35 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0225 others(32): Show |
35 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.93-7850_93-7849dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752538 | |||||||
chr5:131752779 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.93-8089A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752779 | |||||||
chr5:131752793 | C | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.93-8103G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752793 | |||||||
chr5:131752807 | C | A | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-8117G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752807 | |||||||
chr5:131752884 | A | G | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-8194T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131752884 | |||||||
chr5:131753138 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.93-8448C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753138 | |||||||
chr5:131753142 | C | T | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-8452G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753142 | |||||||
chr5:131753306 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0199 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.93-8616C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753306 | |||||||
chr5:131753341 | T | G | 38 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(35): Show |
38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.93-8651A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753341 | |||||||
chr5:131753351 | A | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-8661T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753351 | |||||||
chr5:131753386 | G | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-8696C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753386 | |||||||
chr5:131753409 | T | C | 2 | a0002c0002t0002g0163 a0002c0002t0002g0273 |
2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.93-8719A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753409 | |||||||
chr5:131753540 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.93-8850T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753540 | |||||||
chr5:131753574 | G | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(15): Show |
18 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.93-8884C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753574 | |||||||
chr5:131753612 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0005g0080 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.93-8922A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753612 | |||||||
chr5:131753664 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.93-8974A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753664 | |||||||
chr5:131753817 | A | AT | 6 | a0001c0001t0001g0234 a0001c0001t0002g0004 a0001c0001t0002g0098 others(3): Show |
6 | NA18956.hp2 NA18978.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-9128dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753817 | |||||||
chr5:131753848 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-9158A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753848 | |||||||
chr5:131753971 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-9281C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131753971 | |||||||
chr5:131754176 | C | CT | 277 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(274): Show |
278 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.93-9487dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754176 | |||||||
chr5:131754393 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0002g0107 |
2 | HG02896.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.93-9703G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754393 | |||||||
chr5:131754518 | G | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-9828C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754518 | |||||||
chr5:131754626 | G | C | 1 | a0001c0001t0021g0012 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.93-9936C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754626 | |||||||
chr5:131754749 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10059T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754749 | |||||||
chr5:131754787 | T | C | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.93-10097A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754787 | |||||||
chr5:131754833 | G | A | 1 | a0002c0002t0002g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.93-10143C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131754833 | |||||||
chr5:131755143 | G | A | 2 | a0001c0001t0005g0078 a0001c0001t0005g0114 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.93-10453C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755143 | |||||||
chr5:131755301 | A | C | 10 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
10 | HG00408.hp2 HG02015.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.93-10611T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755301 | |||||||
chr5:131755378 | G | A | 143 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(140): Show |
143 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.93-10688C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755378 | |||||||
chr5:131755396 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-10706T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755396 | |||||||
chr5:131755420 | T | TA | 44 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0074 others(41): Show |
44 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.93-10731dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755420 | |||||||
chr5:131755435 | C | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10745G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755435 | |||||||
chr5:131755452 | A | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-10762T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755452 | |||||||
chr5:131755646 | A | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-10956T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131755646 | |||||||
chr5:131756038 | A | G | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-11348T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756038 | |||||||
chr5:131756696 | G | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-12006C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756696 | |||||||
chr5:131756780 | T | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-12090A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131756780 | |||||||
chr5:131757002 | G | A | 2 | a0002c0002t0004g0007 a0002c0002t0004g0162 |
2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.93-12312C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757002 | |||||||
chr5:131757176 | T | C | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-12486A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757176 | |||||||
chr5:131757290 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.93-12600C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757290 | |||||||
chr5:131757346 | A | T | 4 | a0002c0002t0002g0082 a0002c0002t0002g0141 a0002c0002t0002g0289 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-12656T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131757346 | |||||||
chr5:131758082 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-13392C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758082 | |||||||
chr5:131758276 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.93-13586C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758276 | |||||||
chr5:131758286 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.93-13596G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758286 | |||||||
chr5:131758324 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-13634G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758324 | |||||||
chr5:131758479 | A | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-13789T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758479 | |||||||
chr5:131758709 | A | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-14019T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758709 | |||||||
chr5:131758756 | G | A | 19 | a0001c0001t0002g0113 a0001c0001t0002g0124 a0001c0001t0002g0154 others(16): Show |
19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-14066C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758756 | |||||||
chr5:131758883 | G | A | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-14193C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758883 | |||||||
chr5:131758926 | C | G | 3 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0030 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.93-14236G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131758926 | |||||||
chr5:131759020 | T | A | 1 | a0002c0002t0004g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.93-14330A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759020 | |||||||
chr5:131759299 | ACAGAGAA others(21): Show |
A | 1 | a0001c0001t0009g0170 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.93-14637_93-14610d others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759299 | |||||||
chr5:131759447 | T | C | 41 | a0001c0001t0001g0064 a0001c0001t0003g0020 a0001c0001t0003g0021 others(38): Show |
41 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.93-14757A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759447 | |||||||
chr5:131759614 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-14924C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759614 | |||||||
chr5:131759616 | G | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-14926C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759616 | |||||||
chr5:131759827 | G | C | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-15137C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759827 | |||||||
chr5:131759836 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.93-15146G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759836 | |||||||
chr5:131759900 | T | C | 1 | a0004c0007t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.93-15210A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759900 | |||||||
chr5:131759944 | G | T | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.93-15254C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131759944 | |||||||
chr5:131760272 | T | C | 1 | a0001c0001t0005g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.93-15582A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760272 | |||||||
chr5:131760456 | T | G | 1 | a0001c0001t0012g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93-15766A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760456 | |||||||
chr5:131760590 | T | G | 1 | a0001c0001t0005g0092 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.93-15900A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760590 | |||||||
chr5:131760775 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-16085G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760775 | |||||||
chr5:131760955 | C | G | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-16265G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760955 | |||||||
chr5:131760984 | C | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-16294G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131760984 | |||||||
chr5:131761088 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-16398G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761088 | |||||||
chr5:131761157 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-16467T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761157 | |||||||
chr5:131761640 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-16950C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131761640 | |||||||
chr5:131762527 | G | A | 51 | a0001c0001t0002g0275 a0001c0001t0005g0050 a0002c0002t0002g0003 others(48): Show |
52 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.93-17837C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762527 | |||||||
chr5:131762604 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-17914C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762604 | |||||||
chr5:131762853 | A | G | 19 | a0001c0001t0002g0113 a0001c0001t0002g0124 a0001c0001t0002g0154 others(16): Show |
19 | HG00738.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-18163T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131762853 | |||||||
chr5:131763113 | G | T | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-18423C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763113 | |||||||
chr5:131763288 | T | TAC | 52 | a0001c0001t0002g0076 a0001c0001t0002g0081 a0001c0001t0002g0101 others(49): Show |
53 | HG00408.hp1 HG00642.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.93-18600_93-18599d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | T | TACAC | 54 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0054 others(51): Show |
55 | HG00544.hp2 HG00738.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.93-18602_93-18599d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | T | TACACAC | 11 | a0001c0001t0002g0089 a0001c0001t0002g0097 a0001c0001t0002g0099 others(8): Show |
11 | HG02015.hp1 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-18604_93-18599d others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | T | TACACACA others(1): Show |
15 | a0001c0001t0001g0303 a0001c0001t0002g0155 a0001c0001t0003g0025 others(12): Show |
15 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.93-18606_93-18599d others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | T | TACACACA others(3): Show |
3 | a0001c0001t0003g0029 a0001c0001t0003g0309 a0001c0001t0012g0044 |
3 | HG00639.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.93-18608_93-18599d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.93-18610_93-18599d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | TAC | T | 5 | a0001c0001t0001g0064 a0001c0001t0002g0108 a0001c0016t0001g0063 others(2): Show |
5 | HG00438.hp1 HG02135.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-18600_93-18599d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | TACAC | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-18602_93-18599d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | TACACACA others(5): Show |
T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-18610_93-18599d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | TACACACA others(7): Show |
T | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.93-18612_93-18599d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763288 | TACACACA others(9): Show |
T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-18614_93-18599d others(18): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763288 | |||||||
chr5:131763349 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0007g0023 a0001c0001t0007g0024 others(1): Show |
4 | HG01123.hp2 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-18659A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763349 | |||||||
chr5:131763413 | T | C | 48 | a0001c0001t0001g0064 a0001c0001t0001g0303 a0001c0001t0003g0020 others(45): Show |
48 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.93-18723A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763413 | |||||||
chr5:131763453 | T | C | 39 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(36): Show |
39 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.93-18763A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763453 | |||||||
chr5:131763534 | C | T | 141 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(138): Show |
141 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.93-18844G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131763534 | |||||||
chr5:131764100 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0006g0297 |
2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.93-19410G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764100 | |||||||
chr5:131764181 | A | C | 1 | a0003c0003t0002g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.93-19491T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764181 | |||||||
chr5:131764307 | C | CT | 11 | a0001c0001t0001g0186 a0001c0001t0001g0201 a0001c0001t0002g0098 others(8): Show |
11 | HG01496.hp1 HG02015.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-19618dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | |||||||
chr5:131764307 | C | CTT | 9 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0224 others(6): Show |
9 | HG00408.hp2 HG02040.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.93-19619_93-19618d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | |||||||
chr5:131764307 | CT | C | 17 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0236 others(14): Show |
17 | HG00639.hp1 HG02572.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.93-19618delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764307 | |||||||
chr5:131764432 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-19742C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764432 | |||||||
chr5:131764447 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0211 others(8): Show |
11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.93-19757C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764447 | |||||||
chr5:131764553 | T | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.93-19863A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764553 | |||||||
chr5:131764732 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.93-20042G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131764732 | |||||||
chr5:131765496 | T | C | 38 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(35): Show |
38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.93-20806A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131765496 | |||||||
chr5:131766132 | C | T | 1 | a0002c0002t0004g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.93-21442G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766132 | |||||||
chr5:131766215 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-21525T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766215 | |||||||
chr5:131766252 | G | A | 8 | a0001c0001t0001g0303 a0001c0001t0003g0304 a0001c0001t0003g0305 others(5): Show |
8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-21562C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766252 | |||||||
chr5:131766255 | T | G | 8 | a0001c0001t0001g0303 a0001c0001t0003g0304 a0001c0001t0003g0305 others(5): Show |
8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.93-21565A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766255 | |||||||
chr5:131766291 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.93-21601G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766291 | |||||||
chr5:131766361 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.93-21671G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766361 | |||||||
chr5:131766417 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.93-21727G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766417 | |||||||
chr5:131766444 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.93-21754C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766444 | |||||||
chr5:131766501 | T | C | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.93-21811A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766501 | |||||||
chr5:131766505 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-21815G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766505 | |||||||
chr5:131766577 | G | C | 1 | a0002c0002t0004g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.93-21887C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766577 | |||||||
chr5:131766869 | T | G | 3 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0264 |
3 | HG02165.hp2 HG04184.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.93-22179A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766869 | |||||||
chr5:131766899 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.93-22209G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766899 | |||||||
chr5:131766901 | C | T | 1 | a0003c0003t0002g0312 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.93-22211G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766901 | |||||||
chr5:131766952 | T | C | 1 | a0001c0001t0005g0280 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.93-22262A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131766952 | |||||||
chr5:131767121 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22431A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767121 | |||||||
chr5:131767129 | T | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-22439A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767129 | |||||||
chr5:131767209 | A | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22519T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767209 | |||||||
chr5:131767238 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-22548G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767238 | |||||||
chr5:131767277 | C | T | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-22587G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767277 | |||||||
chr5:131767361 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.93-22671C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767361 | |||||||
chr5:131767427 | C | CA | 9 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0260 others(6): Show |
9 | HG01884.hp2 HG01981.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.93-22738dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0007g0023 a0001c0001t0007g0024 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.93-22747_93-22738d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0007g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93-22748_93-22738d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CA | C | 182 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(179): Show |
184 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.93-22738delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAA | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0187 a0001c0001t0001g0212 others(5): Show |
8 | HG01069.hp1 HG01256.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-22739_93-22738d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAAA | C | 11 | a0001c0001t0002g0055 a0003c0003t0002g0311 a0003c0003t0002g0312 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-22740_93-22738d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAAAAAAA others(3): Show |
C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-22747_93-22738d others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.93-22748_93-22738d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAAAAAAA others(7): Show |
C | 32 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.93-22751_93-22738d others(16): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131767427 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0202 a0001c0001t0001g0239 |
3 | HG00438.hp2 NA18979.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.93-22752_93-22738d others(17): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131767427 | |||||||
chr5:131768033 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-23343C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768033 | |||||||
chr5:131768465 | GT | G | 70 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0172 others(67): Show |
70 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.93-23776delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768465 | |||||||
chr5:131768465 | GTT | G | 138 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(135): Show |
138 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.93-23777_93-23776d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768465 | |||||||
chr5:131768480 | T | A | 1 | a0001c0012t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.93-23790A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768480 | |||||||
chr5:131768493 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.93-23803T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768493 | |||||||
chr5:131768566 | T | G | 16 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(13): Show |
16 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.93-23876A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768566 | |||||||
chr5:131768581 | G | A | 1 | a0002c0002t0017g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.93-23891C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768581 | |||||||
chr5:131768707 | G | A | 2 | a0001c0001t0008g0019 a0001c0001t0008g0047 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.93-24017C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768707 | |||||||
chr5:131768712 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-24022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768712 | |||||||
chr5:131768723 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.93-24033G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768723 | |||||||
chr5:131768800 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0211 others(8): Show |
11 | NA18939.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.93-24110T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131768800 | |||||||
chr5:131769155 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.93-24465C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769155 | |||||||
chr5:131769489 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.93-24799G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769489 | |||||||
chr5:131769536 | G | T | 1 | a0006c0010t0001g0292 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.93-24846C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769536 | |||||||
chr5:131769655 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.93-24965C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769655 | |||||||
chr5:131769778 | TGAA | T | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-25091_93-25089d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769778 | |||||||
chr5:131769779 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93-25089C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769779 | |||||||
chr5:131769808 | T | G | 1 | a0003c0003t0002g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.93-25118A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769808 | |||||||
chr5:131769826 | C | T | 1 | a0001c0001t0007g0024 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.93-25136G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769826 | |||||||
chr5:131769843 | A | C | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-25153T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769843 | |||||||
chr5:131769989 | C | T | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.93-25299G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131769989 | |||||||
chr5:131770211 | G | A | 1 | a0002c0002t0005g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.93-25521C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770211 | |||||||
chr5:131770259 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.93-25569C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770259 | |||||||
chr5:131770458 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(17): Show |
20 | HG00438.hp2 HG00609.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.93-25768G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770458 | |||||||
chr5:131770756 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0199 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.93-26066G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770756 | |||||||
chr5:131770874 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.92+25956A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770874 | |||||||
chr5:131770917 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.92+25913T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131770917 | |||||||
chr5:131771069 | C | T | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+25761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771069 | |||||||
chr5:131771078 | T | C | 2 | a0001c0001t0005g0118 a0001c0001t0005g0156 |
2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.92+25752A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771078 | |||||||
chr5:131771303 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+25527G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771303 | |||||||
chr5:131771357 | C | A | 1 | a0003c0003t0002g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.92+25473G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771357 | |||||||
chr5:131771434 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+25396A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771434 | |||||||
chr5:131771688 | T | G | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.92+25142A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771688 | |||||||
chr5:131771689 | C | T | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.92+25141G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771689 | |||||||
chr5:131771693 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+25137C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771693 | |||||||
chr5:131771808 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.92+25022A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771808 | |||||||
chr5:131771999 | G | A | 45 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(42): Show |
45 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.92+24831C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131771999 | |||||||
chr5:131772000 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+24830C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772000 | |||||||
chr5:131772009 | C | A | 1 | a0001c0008t0002g0111 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.92+24821G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772009 | |||||||
chr5:131772255 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+24575T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772255 | |||||||
chr5:131772382 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+24448G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772382 | |||||||
chr5:131772420 | CA | C | 16 | a0001c0001t0002g0096 a0001c0001t0002g0113 a0001c0001t0002g0166 others(13): Show |
16 | HG01168.hp2 HG01255.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.92+24409delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | |||||||
chr5:131772420 | CAA | C | 20 | a0001c0001t0001g0177 a0001c0001t0001g0201 a0001c0001t0001g0295 others(17): Show |
20 | HG01081.hp1 HG01175.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+24408_92+24409d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | |||||||
chr5:131772420 | CAAA | C | 154 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(151): Show |
154 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.92+24407_92+24409d others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | |||||||
chr5:131772420 | CAAAA | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
23 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.92+24406_92+24409d others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772420 | |||||||
chr5:131772603 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+24227G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772603 | |||||||
chr5:131772726 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.92+24104A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772726 | |||||||
chr5:131772772 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.92+24058G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772772 | |||||||
chr5:131772837 | A | G | 4 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 others(1): Show |
4 | HG00733.hp2 HG01256.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+23993T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772837 | |||||||
chr5:131772921 | T | C | 1 | a0001c0001t0007g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92+23909A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131772921 | |||||||
chr5:131773097 | T | C | 1 | a0001c0001t0005g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.92+23733A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773097 | |||||||
chr5:131773156 | G | T | 32 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+23674C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773156 | |||||||
chr5:131773157 | C | T | 32 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+23673G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773157 | |||||||
chr5:131773245 | T | C | 2 | a0001c0001t0005g0050 a0002c0002t0004g0144 |
2 | NA18942.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.92+23585A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773245 | |||||||
chr5:131773274 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+23556C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773274 | |||||||
chr5:131773493 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+23337C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773493 | |||||||
chr5:131773548 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.92+23282G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773548 | |||||||
chr5:131773660 | C | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+23170G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773660 | |||||||
chr5:131773747 | A | G | 1 | a0002c0006t0004g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92+23083T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773747 | |||||||
chr5:131773852 | G | T | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+22978C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131773852 | |||||||
chr5:131774099 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+22731A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774099 | |||||||
chr5:131774395 | C | T | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92+22435G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774395 | |||||||
chr5:131774398 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92+22432A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774398 | |||||||
chr5:131774432 | C | A | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.92+22398G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774432 | |||||||
chr5:131774580 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.92+22250C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774580 | |||||||
chr5:131774710 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92+22120A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774710 | |||||||
chr5:131774887 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.92+21943T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131774887 | |||||||
chr5:131775088 | A | G | 1 | a0006c0010t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.92+21742T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775088 | |||||||
chr5:131775165 | A | G | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+21665T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775165 | |||||||
chr5:131775463 | C | CAACT | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+21366_92+21367i others(6): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775463 | |||||||
chr5:131775528 | C | CT | 16 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0085 others(13): Show |
16 | HG02615.hp1 HG03041.hp1 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.92+21301dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775528 | |||||||
chr5:131775528 | CT | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0178 a0001c0001t0001g0188 others(20): Show |
23 | HG01070.hp2 HG01167.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.92+21301delA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775528 | |||||||
chr5:131775621 | G | A | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92+21209C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775621 | |||||||
chr5:131775667 | G | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+21163C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775667 | |||||||
chr5:131775684 | C | T | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.92+21146G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775684 | |||||||
chr5:131775712 | G | A | 47 | a0001c0001t0001g0064 a0001c0001t0001g0303 a0001c0001t0003g0020 others(44): Show |
47 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.92+21118C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775712 | |||||||
chr5:131775775 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+21055C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775775 | |||||||
chr5:131775970 | T | G | 1 | a0001c0001t0006g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.92+20860A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131775970 | |||||||
chr5:131776260 | G | T | 1 | a0002c0002t0004g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.92+20570C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776260 | |||||||
chr5:131776417 | G | A | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.92+20413C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776417 | |||||||
chr5:131776429 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.92+20401A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776429 | |||||||
chr5:131776445 | A | G | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+20385T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776445 | |||||||
chr5:131776516 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+20314C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776516 | |||||||
chr5:131776550 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92+20280G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776550 | |||||||
chr5:131776686 | T | A | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92+20144A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776686 | |||||||
chr5:131776934 | C | T | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+19896G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131776934 | |||||||
chr5:131777137 | CAT | C | 6 | a0003c0003t0002g0311 a0003c0003t0002g0314 a0003c0003t0002g0315 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+19691_92+19692d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777137 | |||||||
chr5:131777227 | C | A | 2 | a0001c0001t0001g0064 a0001c0016t0001g0063 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.92+19603G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777227 | |||||||
chr5:131777227 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+19603G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777227 | |||||||
chr5:131777251 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0198 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.92+19579A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777251 | |||||||
chr5:131777402 | G | A | 6 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(3): Show |
6 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+19428C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777402 | |||||||
chr5:131777637 | A | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+19193T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131777637 | |||||||
chr5:131778036 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+18794T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778036 | |||||||
chr5:131778047 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0005g0080 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.92+18783C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778047 | |||||||
chr5:131778121 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.92+18709C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778121 | |||||||
chr5:131778137 | C | T | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+18693G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778137 | |||||||
chr5:131778257 | C | G | 1 | a0001c0001t0002g0113 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.92+18573G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778257 | |||||||
chr5:131778402 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+18428A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778402 | |||||||
chr5:131778472 | C | T | 1 | a0001c0001t0005g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.92+18358G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778472 | |||||||
chr5:131778473 | G | C | 184 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(181): Show |
184 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.92+18357C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778473 | |||||||
chr5:131778514 | G | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+18316C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778514 | |||||||
chr5:131778688 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92+18142G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778688 | |||||||
chr5:131778835 | T | G | 1 | a0004c0007t0001g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.92+17995A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778835 | |||||||
chr5:131778840 | T | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+17990A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778840 | |||||||
chr5:131778848 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.92+17982C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778848 | |||||||
chr5:131778868 | C | T | 1 | a0001c0016t0001g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92+17962G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778868 | |||||||
chr5:131778890 | G | A | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+17940C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778890 | |||||||
chr5:131778913 | G | A | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+17917C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778913 | |||||||
chr5:131778964 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.92+17866C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131778964 | |||||||
chr5:131779069 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+17761G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779069 | |||||||
chr5:131779135 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.92+17695A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779135 | |||||||
chr5:131779147 | TA | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0177 a0001c0001t0001g0190 others(6): Show |
9 | HG01070.hp1 HG01943.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+17682delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779147 | |||||||
chr5:131779194 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+17636C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779194 | |||||||
chr5:131779213 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+17617A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779213 | |||||||
chr5:131779286 | A | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
144 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.92+17544T>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779286 | |||||||
chr5:131779372 | G | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+17458C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779372 | |||||||
chr5:131779382 | T | G | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.92+17448A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779382 | |||||||
chr5:131779504 | C | A | 1 | a0003c0003t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92+17326G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779504 | |||||||
chr5:131779516 | T | TA | 76 | a0001c0001t0002g0081 a0001c0001t0002g0113 a0001c0001t0002g0124 others(73): Show |
77 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.92+17313dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779516 | |||||||
chr5:131779531 | T | A | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+17299A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779531 | |||||||
chr5:131779556 | C | T | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+17274G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779556 | |||||||
chr5:131779580 | C | T | 1 | a0001c0004t0001g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.92+17250G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779580 | |||||||
chr5:131779655 | T | C | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+17175A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779655 | |||||||
chr5:131779687 | C | CA | 6 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(3): Show |
6 | HG01496.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+17142dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779687 | |||||||
chr5:131779687 | CA | C | 11 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0231 others(8): Show |
11 | HG01169.hp2 HG01257.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+17142delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779687 | |||||||
chr5:131779781 | T | C | 4 | a0002c0002t0002g0125 a0002c0002t0002g0163 a0002c0002t0002g0273 others(1): Show |
4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+17049A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131779781 | |||||||
chr5:131780046 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0002c0002t0018g0059 |
3 | HG02486.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.92+16784A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780046 | |||||||
chr5:131780276 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92+16554A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780276 | |||||||
chr5:131780362 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+16468T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780362 | |||||||
chr5:131780389 | C | A | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.92+16441G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780389 | |||||||
chr5:131780538 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0266 |
2 | HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.92+16292A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780538 | |||||||
chr5:131780631 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.92+16199C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780631 | |||||||
chr5:131780688 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+16142C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131780688 | |||||||
chr5:131781128 | G | A | 1 | a0002c0002t0002g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.92+15702C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781128 | |||||||
chr5:131781206 | T | C | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+15624A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781206 | |||||||
chr5:131781580 | A | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+15250T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781580 | |||||||
chr5:131781833 | A | C | 2 | a0001c0001t0002g0096 a0001c0001t0005g0277 |
2 | HG01099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.92+14997T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781833 | |||||||
chr5:131781851 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.92+14979C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781851 | |||||||
chr5:131781899 | T | C | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+14931A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131781899 | |||||||
chr5:131782167 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+14663A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782167 | |||||||
chr5:131782225 | C | A | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+14605G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782225 | |||||||
chr5:131782319 | C | T | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+14511G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782319 | |||||||
chr5:131782375 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92+14455G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782375 | |||||||
chr5:131782407 | C | A | 189 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(186): Show |
189 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(186): Show |
intron_variant | MODIFIER | c.92+14423G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782407 | |||||||
chr5:131782472 | C | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(199): Show |
202 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.92+14358G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782472 | |||||||
chr5:131782650 | T | C | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+14180A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782650 | |||||||
chr5:131782799 | T | C | 42 | a0001c0001t0001g0064 a0001c0001t0001g0303 a0001c0001t0003g0020 others(39): Show |
42 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.92+14031A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782799 | |||||||
chr5:131782954 | C | T | 1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+13876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131782954 | |||||||
chr5:131783000 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92+13830T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783000 | |||||||
chr5:131783045 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92+13785C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783045 | |||||||
chr5:131783131 | T | C | 13 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0085 others(10): Show |
13 | NA18945.hp1 NA18947.hp2 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.92+13699A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783131 | |||||||
chr5:131783250 | T | C | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
142 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.92+13580A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783250 | |||||||
chr5:131783426 | A | G | 1 | a0002c0002t0005g0127 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.92+13404T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783426 | |||||||
chr5:131783453 | C | CA | 6 | a0001c0001t0001g0301 a0001c0001t0002g0055 a0001c0001t0002g0070 others(3): Show |
6 | HG01081.hp1 HG02630.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+13376dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783453 | |||||||
chr5:131783453 | C | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+13377G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783453 | |||||||
chr5:131783494 | A | G | 32 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+13336T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783494 | |||||||
chr5:131783707 | T | G | 5 | a0001c0001t0008g0019 a0001c0001t0008g0045 a0001c0001t0008g0046 others(2): Show |
5 | HG01496.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+13123A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131783707 | |||||||
chr5:131784008 | C | CA | 141 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
141 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.92+12821dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784008 | |||||||
chr5:131784141 | G | T | 1 | a0001c0001t0002g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.92+12689C>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784141 | |||||||
chr5:131784244 | G | A | 1 | a0002c0002t0002g0146 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.92+12586C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784244 | |||||||
chr5:131784255 | T | C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+12575A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784255 | |||||||
chr5:131784517 | T | C | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+12313A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784517 | |||||||
chr5:131784609 | C | G | 1 | a0002c0006t0004g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.92+12221G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784609 | |||||||
chr5:131784614 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.92+12216T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784614 | |||||||
chr5:131784645 | A | AC | 17 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0002g0083 others(14): Show |
17 | HG01081.hp1 HG02486.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.92+12184dupG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784645 | |||||||
chr5:131784874 | A | C | 1 | a0001c0001t0002g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.92+11956T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784874 | |||||||
chr5:131784895 | G | A | 2 | a0001c0005t0006g0066 a0001c0005t0006g0071 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.92+11935C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784895 | |||||||
chr5:131784932 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+11898G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131784932 | |||||||
chr5:131785001 | TATATGAC others(21): Show |
T | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.92+11801_92+11828d others(30): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785001 | |||||||
chr5:131785008 | CTATATAT others(65): Show |
C | 5 | a0003c0003t0002g0311 a0003c0003t0002g0315 a0003c0003t0002g0316 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+11750_92+11821d others(74): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785008 | |||||||
chr5:131785009 | TATATATA others(13): Show |
T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0206 a0001c0001t0006g0258 others(6): Show |
9 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+11801_92+11820d others(22): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | |||||||
chr5:131785009 | TATATATA others(63): Show |
T | 3 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 |
3 | HG02809.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92+11751_92+11820d others(72): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | |||||||
chr5:131785009 | TATATATA others(130): Show |
T | 3 | a0001c0001t0001g0064 a0001c0016t0001g0063 a0009c0015t0001g0192 |
3 | HG02559.hp2 HG02809.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.92+11684_92+11820d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785009 | |||||||
chr5:131785011 | TATATATG others(11): Show |
T | 145 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.92+11801_92+11818d others(20): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | |||||||
chr5:131785011 | TATATATG others(95): Show |
T | 20 | a0001c0001t0001g0177 a0001c0001t0001g0190 a0001c0001t0001g0193 others(17): Show |
20 | HG00642.hp1 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+11717_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | |||||||
chr5:131785011 | TATATATG others(128): Show |
T | 11 | a0001c0001t0001g0056 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+11684_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | |||||||
chr5:131785011 | TATATATG others(160): Show |
T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.92+11652_92+11818d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785011 | |||||||
chr5:131785028 | A | ACTATATA others(3): Show |
1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11801_92+11802i others(12): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785028 | |||||||
chr5:131785028 | A | ACTATATA others(5): Show |
1 | a0003c0003t0002g0317 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+11801_92+11802i others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785028 | |||||||
chr5:131785029 | CATATATA others(109): Show |
C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+11685_92+11800d others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785029 | |||||||
chr5:131785038 | G | C | 1 | a0002c0002t0004g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.92+11792C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785038 | |||||||
chr5:131785049 | CTATATAT others(24): Show |
C | 9 | a0001c0001t0001g0230 a0001c0001t0003g0025 a0001c0001t0003g0026 others(6): Show |
9 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+11750_92+11780d others(33): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785049 | |||||||
chr5:131785049 | CTATATAT others(47): Show |
C | 1 | a0003c0003t0002g0314 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.92+11727_92+11780d others(56): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785049 | |||||||
chr5:131785050 | TATATATA others(56): Show |
T | 24 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0303 others(21): Show |
24 | HG00639.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.92+11717_92+11779d others(65): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785050 | |||||||
chr5:131785050 | TATATATA others(89): Show |
T | 116 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(113): Show |
116 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.92+11684_92+11779d others(98): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785050 | |||||||
chr5:131785058 | TCATATAT others(14): Show |
T | 4 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0317 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+11751_92+11771d others(23): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785058 | |||||||
chr5:131785059 | C | G | 2 | a0001c0001t0001g0227 a0001c0014t0001g0326 |
2 | HG02602.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.92+11771G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785059 | |||||||
chr5:131785059 | CATATATA others(15): Show |
C | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11749_92+11770d others(24): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785059 | |||||||
chr5:131785068 | GATATATA others(35): Show |
G | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11720_92+11761d others(44): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785068 | |||||||
chr5:131785069 | ATATATAT others(68): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.92+11686_92+11760d others(77): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785069 | |||||||
chr5:131785079 | CAT | C | 5 | a0001c0001t0002g0055 a0001c0001t0002g0124 a0001c0001t0002g0166 others(2): Show |
5 | HG01081.hp1 HG02735.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+11749_92+11750d others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785079 | |||||||
chr5:131785081 | T | TATATATA others(25): Show |
2 | a0002c0002t0004g0164 a0008c0011t0005g0121 |
2 | NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.92+11717_92+11748d others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785081 | |||||||
chr5:131785081 | T | TC | 4 | a0003c0003t0002g0312 a0003c0003t0002g0313 a0003c0003t0002g0317 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+11748_92+11749i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785081 | |||||||
chr5:131785096 | T | C | 2 | a0002c0002t0002g0158 a0002c0002t0002g0272 |
2 | HG00544.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.92+11734A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785096 | |||||||
chr5:131785102 | TATATATA others(4): Show |
T | 3 | a0001c0005t0001g0067 a0001c0005t0001g0068 a0001c0005t0001g0069 |
3 | HG02809.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.92+11717_92+11727d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785102 | |||||||
chr5:131785109 | ATATCATA others(28): Show |
A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+11686_92+11720d others(37): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785109 | |||||||
chr5:131785111 | A | ATCATATA others(26): Show |
4 | a0002c0002t0002g0125 a0002c0002t0002g0163 a0002c0002t0002g0273 others(1): Show |
4 | HG02602.hp2 HG03239.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+11686_92+11718d others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | |||||||
chr5:131785111 | A | ATCATATA others(58): Show |
1 | a0002c0002t0002g0148 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.92+11718_92+11719i others(67): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | |||||||
chr5:131785111 | ATCATATA others(26): Show |
A | 5 | a0001c0001t0002g0081 a0001c0001t0002g0275 a0001c0001t0005g0079 others(2): Show |
5 | HG02015.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+11686_92+11718d others(35): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785111 | |||||||
chr5:131785112 | T | C | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11718A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785112 | |||||||
chr5:131785113 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+11717G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785113 | |||||||
chr5:131785134 | TATATATA others(5): Show |
T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0190 a0001c0001t0001g0193 others(2): Show |
5 | HG00544.hp1 HG01070.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+11684_92+11695d others(14): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785134 | |||||||
chr5:131785143 | AG | A | 57 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0303 others(54): Show |
57 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.92+11686delC | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785143 | |||||||
chr5:131785144 | G | GTCATATA others(25): Show |
2 | a0002c0002t0004g0120 a0002c0002t0004g0162 |
2 | NA18942.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.92+11654_92+11685d others(34): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785144 | |||||||
chr5:131785145 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0002g0166 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.92+11685A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785145 | |||||||
chr5:131785146 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0322 |
2 | HG02602.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.92+11684G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785146 | |||||||
chr5:131785155 | G | C | 1 | a0001c0001t0002g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.92+11675C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785155 | |||||||
chr5:131785167 | TATATATA others(4): Show |
T | 11 | a0001c0001t0001g0056 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
11 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.92+11652_92+11662d others(13): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785167 | |||||||
chr5:131785176 | A | AG | 33 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(30): Show |
33 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.92+11653_92+11654i others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785176 | |||||||
chr5:131785176 | A | G | 3 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 |
3 | HG00733.hp2 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.92+11654T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785176 | |||||||
chr5:131785327 | G | A | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+11503C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785327 | |||||||
chr5:131785346 | G | C | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+11484C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785346 | |||||||
chr5:131785427 | C | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+11403G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785427 | |||||||
chr5:131785472 | T | C | 4 | a0002c0002t0002g0006 a0002c0002t0002g0148 a0002c0002t0002g0149 others(1): Show |
4 | HG00733.hp2 HG01256.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+11358A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785472 | |||||||
chr5:131785550 | CA | C | 251 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(248): Show |
252 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(249): Show |
intron_variant | MODIFIER | c.92+11279delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785550 | |||||||
chr5:131785733 | A | G | 1 | a0001c0005t0006g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+11097T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785733 | |||||||
chr5:131785950 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.92+10880G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785950 | |||||||
chr5:131785954 | C | T | 3 | a0004c0007t0001g0176 a0004c0007t0001g0183 a0004c0007t0001g0184 |
3 | HG02976.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+10876G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131785954 | |||||||
chr5:131786072 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.92+10758A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786072 | |||||||
chr5:131786205 | T | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+10625A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786205 | |||||||
chr5:131786295 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.92+10535G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786295 | |||||||
chr5:131786310 | C | A | 8 | a0001c0001t0001g0303 a0001c0001t0003g0304 a0001c0001t0003g0305 others(5): Show |
8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+10520G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786310 | |||||||
chr5:131786411 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.92+10419C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786411 | |||||||
chr5:131786790 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.92+10040G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786790 | |||||||
chr5:131786810 | A | C | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+10020T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131786810 | |||||||
chr5:131787230 | GC | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0228 a0001c0001t0023g0229 |
3 | HG00609.hp2 NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.92+9599delG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787230 | |||||||
chr5:131787581 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.92+9249A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787581 | |||||||
chr5:131787702 | T | C | 38 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(35): Show |
38 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.92+9128A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787702 | |||||||
chr5:131787894 | C | T | 1 | a0009c0015t0001g0192 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.92+8936G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787894 | |||||||
chr5:131787899 | T | C | 2 | a0004c0007t0001g0183 a0004c0007t0001g0184 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.92+8931A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131787899 | |||||||
chr5:131788019 | C | T | 2 | a0001c0001t0007g0023 a0001c0001t0007g0075 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+8811G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788019 | |||||||
chr5:131788049 | A | C | 201 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
201 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.92+8781T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788049 | |||||||
chr5:131788072 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+8758G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788072 | |||||||
chr5:131788079 | T | A | 1 | a0002c0002t0004g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.92+8751A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788079 | |||||||
chr5:131788296 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.92+8534T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788296 | |||||||
chr5:131788407 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+8423C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788407 | |||||||
chr5:131788557 | T | G | 32 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(29): Show |
32 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.92+8273A>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788557 | |||||||
chr5:131788694 | C | CA | 13 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0165 others(10): Show |
13 | HG00544.hp2 HG02040.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+8135dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788694 | |||||||
chr5:131788694 | CA | C | 56 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(53): Show |
56 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.92+8135delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788694 | |||||||
chr5:131788847 | A | G | 1 | a0002c0002t0002g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92+7983T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788847 | |||||||
chr5:131788945 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.92+7885C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788945 | |||||||
chr5:131788972 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+7858A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131788972 | |||||||
chr5:131789260 | G | A | 2 | a0002c0002t0002g0160 a0002c0002t0002g0161 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.92+7570C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789260 | |||||||
chr5:131789387 | T | A | 203 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
203 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.92+7443A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789387 | |||||||
chr5:131789588 | C | T | 6 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+7242G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789588 | |||||||
chr5:131789591 | C | T | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+7239G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789591 | |||||||
chr5:131789716 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.92+7114A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131789716 | |||||||
chr5:131790066 | C | T | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+6764G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790066 | |||||||
chr5:131790185 | A | G | 1 | a0002c0002t0018g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92+6645T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790185 | |||||||
chr5:131790295 | G | A | 55 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(52): Show |
55 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.92+6535C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790295 | |||||||
chr5:131790434 | G | A | 2 | a0005c0009t0014g0051 a0005c0009t0015g0052 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.92+6396C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790434 | |||||||
chr5:131790478 | C | CA | 65 | a0001c0001t0001g0322 a0001c0001t0002g0054 a0001c0001t0002g0055 others(62): Show |
66 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.92+6351dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | C | CAA | 33 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
33 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.92+6350_92+6351dup others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | C | CAAA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0056 others(63): Show |
66 | HG00408.hp2 HG00639.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.92+6349_92+6351dup others(3): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | C | CAAAA | 56 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0228 others(53): Show |
56 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.92+6348_92+6351dup others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | C | CAAAAA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01978.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+6347_92+6351dup others(5): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | C | CAAAAAAA others(3): Show |
1 | a0001c0012t0001g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.92+6342_92+6351dup others(10): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790478 | CAAAAAAA others(1): Show |
C | 31 | a0001c0001t0001g0303 a0001c0001t0003g0020 a0001c0001t0003g0021 others(28): Show |
31 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.92+6344_92+6351del others(8): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790478 | |||||||
chr5:131790639 | GAAGA | G | 3 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0075 |
3 | HG02109.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.92+6187_92+6190del others(4): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131790639 | |||||||
chr5:131791334 | C | T | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+5496G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791334 | |||||||
chr5:131791594 | A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+5236T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791594 | |||||||
chr5:131791608 | A | G | 1 | a0002c0002t0002g0003 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.92+5222T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791608 | |||||||
chr5:131791857 | T | A | 12 | a0001c0001t0001g0064 a0001c0016t0001g0063 a0003c0003t0002g0311 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.92+4973A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791857 | |||||||
chr5:131791878 | GA | G | 140 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
140 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.92+4951delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791878 | |||||||
chr5:131791923 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.92+4907A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791923 | |||||||
chr5:131791940 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0290 |
3 | HG02055.hp1 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.92+4890G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791940 | |||||||
chr5:131791981 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+4849G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131791981 | |||||||
chr5:131792160 | C | CT | 54 | a0001c0001t0001g0064 a0001c0001t0001g0171 a0001c0001t0001g0172 others(51): Show |
54 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.92+4669dupA | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792160 | |||||||
chr5:131792213 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92+4617A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792213 | |||||||
chr5:131792213 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.92+4617A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792213 | |||||||
chr5:131792222 | G | A | 1 | a0003c0003t0002g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92+4608C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792222 | |||||||
chr5:131792307 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92+4523G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792307 | |||||||
chr5:131792345 | G | C | 1 | a0001c0001t0005g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92+4485C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792345 | |||||||
chr5:131792658 | G | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+4172C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792658 | |||||||
chr5:131792722 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.92+4108T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792722 | |||||||
chr5:131792849 | C | G | 1 | a0001c0001t0002g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.92+3981G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792849 | |||||||
chr5:131792857 | C | CA | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
145 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.92+3972dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131792857 | |||||||
chr5:131793083 | T | A | 1 | a0001c0001t0007g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.92+3747A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793083 | |||||||
chr5:131793092 | G | A | 1 | a0002c0002t0002g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.92+3738C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793092 | |||||||
chr5:131793122 | C | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0002g0070 others(6): Show |
9 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+3708G>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793122 | |||||||
chr5:131793496 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92+3334T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793496 | |||||||
chr5:131793499 | A | G | 3 | a0001c0001t0001g0064 a0001c0014t0001g0326 a0001c0016t0001g0063 |
3 | HG02559.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.92+3331T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793499 | |||||||
chr5:131793778 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92+3052A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131793778 | |||||||
chr5:131794174 | A | G | 2 | a0001c0004t0001g0061 a0001c0004t0001g0062 |
2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.92+2656T>C | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794174 | |||||||
chr5:131794229 | T | TA | 29 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0293 others(26): Show |
30 | HG01099.hp1 HG01109.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+2600dupT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | |||||||
chr5:131794229 | TA | T | 52 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(49): Show |
52 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.92+2600delT | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | |||||||
chr5:131794229 | TAA | T | 10 | a0001c0001t0008g0019 a0003c0003t0002g0311 a0003c0003t0002g0312 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+2599_92+2600del others(2): Show |
FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794229 | |||||||
chr5:131794450 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92+2380C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794450 | |||||||
chr5:131794603 | G | A | 1 | a0001c0001t0007g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92+2227C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794603 | |||||||
chr5:131794673 | C | A | 8 | a0001c0001t0001g0303 a0001c0001t0003g0304 a0001c0001t0003g0305 others(5): Show |
8 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+2157G>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794673 | |||||||
chr5:131794815 | A | C | 1 | a0007c0017t0006g0018 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.92+2015T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131794815 | |||||||
chr5:131795230 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG01167.hp1 HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.92+1600T>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795230 | |||||||
chr5:131795486 | T | A | 10 | a0003c0003t0002g0311 a0003c0003t0002g0312 a0003c0003t0002g0313 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+1344A>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795486 | |||||||
chr5:131795538 | T | C | 1 | a0001c0001t0013g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.92+1292A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131795538 | |||||||
chr5:131796114 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+716A>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796114 | |||||||
chr5:131796309 | G | C | 2 | a0001c0001t0007g0323 a0001c0001t0007g0324 |
2 | HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92+521C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796309 | |||||||
chr5:131796453 | C | T | 1 | a0001c0001t0009g0013 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.92+377G>A | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796453 | |||||||
chr5:131796606 | G | C | 1 | a0002c0002t0002g0325 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.92+224C>G | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796606 | |||||||
chr5:131796632 | G | A | 1 | a0001c0014t0001g0326 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92+198C>T | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796632 | |||||||
chr5:131796807 | A | AC | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
10 | HG00438.hp1 HG02738.hp1 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.92+22dupG | FNIP1 | ENSG00000217128.13 | transcript | ENST00000510461.6 | protein_coding | 1/17 | chr5 | 131796807 |