Item | Value |
---|---|
geneid | 60561 |
ensemblid | ENSG00000135249.8 |
hgncid | 21876 |
symbol | RINT1 |
name | RAD50 interactor 1 |
refseq_nuc | NM_021930.6 |
refseq_prot | NP_068749.3 |
ensembl_nuc | ENST00000257700.7 |
ensembl_prot | ENSP00000257700.2 |
mane_status | MANE Select |
chr | chr7 |
start | 105532201 |
end | 105567677 |
strand | + |
ver | v1.2 |
region | chr7:105532201-105567677 |
region5000 | chr7:105527201-105572677 |
regionname0 | RINT1_chr7_105532201_105567677 |
regionname5000 | RINT1_chr7_105527201_105572677 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 792 | 299 | 58 | 61 | 137 | 9 | 32 | 98 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0002 | 0/0 | 792 | 61 | 27 | 15 | 4 | 6 | 9 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0003 | 0/0 | 792 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0004 | 0/0 | 792 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0005 | 0/0 | 792 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0006 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0007 | 0/0 | 792 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
a0008 | 0/0 | 792 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | MLPAG others(787): Show |
chr7 | 105527201 | 105572677 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2376 | 279 | 55 | 60 | 121 | 9 | 32 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0001c0004 | 0/0 | 2376 | 17 | 0 | 1 | 16 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0001c0007 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0001c0011 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0002c0002 | 0/0 | 2376 | 28 | 3 | 6 | 4 | 6 | 9 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0002c0003 | 0/0 | 2376 | 21 | 19 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0002c0005 | 0/0 | 2376 | 7 | 0 | 7 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0002c0006 | 0/0 | 2376 | 5 | 5 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0003c0009 | 0/0 | 2376 | 2 | 1 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0004c0008 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0005c0012 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0006c0014 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0007c0010 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 | ||
a0008c0013 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | ATGCT others(2371): Show |
chr7 | 105527201 | 105572677 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2860 | 234 | 38 | 56 | 103 | 8 | 27 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0001c0001t0002 | 0/0 | 2862 | 14 | 14 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0001c0001t0003 | 0/0 | 2862 | 27 | 2 | 4 | 15 | 1 | 5 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0001c0001t0004 | 0/0 | 2860 | 2 | 0 | 0 | 2 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0001c0001t0006 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0001c0001t0007 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0001c0004t0002 | 0/0 | 2862 | 17 | 0 | 1 | 16 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0001c0007t0001 | 0/0 | 2860 | 2 | 2 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0001c0011t0002 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0002c0002t0002 | 0/0 | 2862 | 28 | 3 | 6 | 4 | 6 | 9 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0002c0003t0002 | 0/0 | 2862 | 20 | 18 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0002c0003t0005 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0002c0005t0002 | 0/0 | 2862 | 7 | 0 | 7 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0002c0006t0002 | 0/0 | 2862 | 5 | 5 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0003c0009t0002 | 0/0 | 2862 | 2 | 1 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2857): Show |
chr7 | 105527201 | 105572677 |
a0004c0008t0001 | 0/0 | 2860 | 2 | 2 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0005c0012t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0006c0014t0001 | 0/0 | 2860 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0007c0010t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
a0008c0013t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | GTGGC others(2855): Show |
chr7 | 105527201 | 105572677 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 2 | 0 | 3 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0001c0011t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0003t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0005t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0006t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0006t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0006t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0006t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0002c0006t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0003c0009t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0003c0009t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0004c0008t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0004c0008t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0005c0012t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0006c0014t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0007c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
a0008c0013t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0012 | EUR | GBR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0086 | EUR | GBR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0235 | EUR | FIN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00544 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00558 | hp2 | a0001 | c0004 | t0002 | g0041 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01109 | hp1 | a0003 | c0009 | t0002 | g0089 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01243 | hp1 | a0002 | c0003 | t0002 | g0068 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0096 | EUR | IBS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0095 | EUR | IBS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01517 | hp2 | a0005 | c0012 | t0001 | g0174 | EUR | IBS | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01884 | hp2 | a0002 | c0003 | t0002 | g0063 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0066 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01928 | hp2 | a0002 | c0005 | t0002 | g0080 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01934 | hp2 | a0002 | c0005 | t0002 | g0081 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01943 | hp1 | a0001 | c0004 | t0002 | g0038 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01943 | hp2 | a0002 | c0005 | t0002 | g0093 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01952 | hp1 | a0002 | c0005 | t0002 | g0013 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01975 | hp1 | a0006 | c0014 | t0001 | g0002 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01981 | hp1 | a0002 | c0005 | t0002 | g0088 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01993 | hp1 | a0002 | c0005 | t0002 | g0012 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02004 | hp2 | a0002 | c0005 | t0002 | g0013 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02055 | hp1 | a0002 | c0003 | t0002 | g0064 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02145 | hp1 | a0003 | c0009 | t0002 | g0085 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | CDX | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02257 | hp2 | a0002 | c0003 | t0002 | g0007 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02258 | hp2 | a0002 | c0003 | t0005 | g0007 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02572 | hp1 | a0002 | c0003 | t0002 | g0026 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02615 | hp1 | a0002 | c0006 | t0002 | g0031 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02630 | hp1 | a0002 | c0006 | t0002 | g0027 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0073 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0007 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02723 | hp1 | a0002 | c0003 | t0002 | g0062 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0058 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0067 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0057 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02976 | hp1 | a0002 | c0003 | t0002 | g0060 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03209 | hp2 | a0002 | c0003 | t0002 | g0069 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03486 | hp1 | a0002 | c0006 | t0002 | g0030 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03486 | hp2 | a0002 | c0006 | t0002 | g0028 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03516 | hp1 | a0002 | c0003 | t0002 | g0065 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03540 | hp1 | a0002 | c0003 | t0002 | g0056 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03579 | hp2 | a0001 | c0011 | t0002 | g0070 | AFR | MSL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03704 | hp2 | a0007 | c0010 | t0001 | g0001 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0076 | SAS | PJL | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0259 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | BEB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | STU | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0229 | AFR | YRI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0061 | AFR | YRI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18945 | hp1 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18950 | hp1 | a0001 | c0004 | t0002 | g0040 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18956 | hp2 | a0008 | c0013 | t0001 | g0113 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18959 | hp1 | a0001 | c0004 | t0002 | g0045 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18970 | hp1 | a0001 | c0004 | t0002 | g0042 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18973 | hp1 | a0001 | c0004 | t0002 | g0015 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18981 | hp2 | a0001 | c0004 | t0002 | g0036 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19003 | hp1 | a0001 | c0004 | t0002 | g0035 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0039 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19030 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0024 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19054 | hp2 | a0001 | c0004 | t0002 | g0046 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19064 | hp1 | a0001 | c0004 | t0002 | g0047 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19065 | hp1 | a0001 | c0004 | t0002 | g0037 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19085 | hp1 | a0001 | c0004 | t0002 | g0034 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19087 | hp2 | a0001 | c0004 | t0002 | g0033 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19091 | hp1 | a0001 | c0004 | t0002 | g0044 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20129 | hp2 | a0002 | c0006 | t0002 | g0029 | AFR | ASW | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0091 | EUR | TSI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0097 | EUR | TSI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02109 | hp1 | a0004 | c0008 | t0001 | g0210 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0098 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02486 | hp1 | a0002 | c0003 | t0002 | g0016 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG06807 | hp1 | a0004 | c0008 | t0001 | g0185 | AFR | USA | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | USA | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18955 | hp1 | a0001 | c0004 | t0002 | g0043 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
NA21309 | hp2 | a0001 | c0007 | t0001 | g0022 | AFR | LWK | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0118 | REF | REF | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0238 | REF | REF | RINT1_chr7_105527201_105572677 | RINT1 | chr7 | 105527201 | 105572677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105536594 | A | T | 2 | a0002 a0003 |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
missense_variant | MODERATE | c.118A>T | p.Ser40Cys | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/15 | 233/2860 | 118/2379 | 40/792 | chr7 | 105536594 | |||
chr7:105542522 | G | A | 1 | a0003 | 2 | HG01109.hp1 HG02145.hp1 |
missense_variant | MODERATE | c.388G>A | p.Ala130Thr | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/15 | 503/2860 | 388/2379 | 130/792 | chr7 | 105542522 | |||
chr7:105550285 | A | T | 1 | a0006 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1132A>T | p.Met378Leu | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/15 | 1247/2860 | 1132/2379 | 378/792 | chr7 | 105550285 | |||
chr7:105551626 | T | C | 1 | a0007 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1390T>C | p.Tyr464His | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/15 | 1505/2860 | 1390/2379 | 464/792 | chr7 | 105551626 | |||
chr7:105563898 | C | T | 1 | a0008 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.1837C>T | p.His613Tyr | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/15 | 1952/2860 | 1837/2379 | 613/792 | chr7 | 105563898 | |||
chr7:105565393 | T | C | 1 | a0004 | 2 | HG02109.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.2003T>C | p.Phe668Ser | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/15 | 2118/2860 | 2003/2379 | 668/792 | chr7 | 105565393 | |||
chr7:105567208 | C | T | 1 | a0005 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.2276C>T | p.Pro759Leu | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 15/15 | 2391/2860 | 2276/2379 | 759/792 | chr7 | 105567208 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105542509 | T | C | 1 | a0001c0007 | 2 | NA18522.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.375T>C | p.Thr125Thr | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/15 | 490/2860 | 375/2379 | 125/792 | chr7 | 105542509 | |||
chr7:105542548 | G | A | 1 | a0002c0003 | 21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
synonymous_variant | LOW | c.414G>A | p.Ala138Ala | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/15 | 529/2860 | 414/2379 | 138/792 | chr7 | 105542548 | |||
chr7:105542599 | C | T | 1 | a0001c0004 | 17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
synonymous_variant | LOW | c.465C>T | p.Ile155Ile | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/15 | 580/2860 | 465/2379 | 155/792 | chr7 | 105542599 | |||
chr7:105551610 | T | C | 1 | a0002c0005 | 7 | HG01928.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
synonymous_variant | LOW | c.1374T>C | p.Ala458Ala | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/15 | 1489/2860 | 1374/2379 | 458/792 | chr7 | 105551610 | |||
chr7:105565352 | G | A | 1 | a0001c0011 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1962G>A | p.Thr654Thr | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/15 | 2077/2860 | 1962/2379 | 654/792 | chr7 | 105565352 | |||
chr7:105567302 | T | C | 1 | a0002c0006 | 5 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.2370T>C | p.Thr790Thr | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 15/15 | 2485/2860 | 2370/2379 | 790/792 | chr7 | 105567302 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105532238 | G | C | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0004t0002 others(7): Show |
97 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-78G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/15 | 78 | chr7 | 105532238 | ||||||
chr7:105532273 | C | T | 1 | a0002c0003t0005 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/15 | 43 | chr7 | 105532273 | ||||||
chr7:105567349 | A | G | 1 | a0001c0001t0007 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 15/15 | 38 | chr7 | 105567349 | ||||||
chr7:105567367 | T | C | 1 | a0001c0001t0006 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 15/15 | 56 | chr7 | 105567367 | ||||||
chr7:105567573 | C | CAA | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0004t0002 others(7): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*262_*263insAA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 15/15 | 263 | chr7 | 105567573 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105532473 | C | A | 1 | a0002c0003t0002g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.42+116C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/14 | chr7 | 105532473 | |||||||
chr7:105532574 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.42+217G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/14 | chr7 | 105532574 | |||||||
chr7:105532582 | T | C | 86 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(83): Show |
96 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.42+225T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/14 | chr7 | 105532582 | |||||||
chr7:105532615 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43-209C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/14 | chr7 | 105532615 | |||||||
chr7:105532634 | C | CT | 35 | a0001c0001t0004g0071 a0002c0002t0002g0012 a0002c0002t0002g0013 others(32): Show |
37 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.43-189dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 105532634 | ||||||
chr7:105533119 | G | C | 1 | a0002c0003t0002g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.88+250G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533119 | |||||||
chr7:105533130 | A | G | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88+261A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533130 | |||||||
chr7:105533326 | C | A | 6 | a0002c0002t0002g0032 a0002c0006t0002g0027 a0002c0006t0002g0028 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+457C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533326 | |||||||
chr7:105533527 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0102 others(55): Show |
62 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.88+658G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533527 | |||||||
chr7:105533903 | T | C | 1 | a0001c0004t0002g0033 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+1034T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533903 | |||||||
chr7:105533937 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.88+1068G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105533937 | |||||||
chr7:105534074 | A | AT | 35 | a0001c0001t0001g0158 a0001c0001t0001g0225 a0001c0001t0002g0059 others(32): Show |
38 | HG01074.hp2 HG01175.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.88+1219dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 105534074 | ||||||
chr7:105534089 | G | A | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+1220G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534089 | |||||||
chr7:105534314 | C | T | 1 | a0002c0003t0002g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+1445C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534314 | |||||||
chr7:105534445 | C | A | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.88+1576C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534445 | |||||||
chr7:105534621 | A | C | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+1752A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534621 | |||||||
chr7:105534762 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-1803G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534762 | |||||||
chr7:105534968 | T | C | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.89-1597T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105534968 | |||||||
chr7:105535026 | A | C | 1 | a0001c0001t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-1539A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535026 | |||||||
chr7:105535205 | C | T | 1 | a0002c0003t0002g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-1360C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535205 | |||||||
chr7:105535229 | C | CT | 37 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0215 others(34): Show |
40 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.89-1318dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 105535229 | ||||||
chr7:105535229 | CT | C | 34 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0002c0002t0002g0012 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.89-1318delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 105535229 | ||||||
chr7:105535291 | G | A | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-1274G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535291 | |||||||
chr7:105535298 | C | T | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-1267C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535298 | |||||||
chr7:105535326 | TTCAAGCG others(7): Show |
T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-1237_89-1224del others(14): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 105535326 | ||||||
chr7:105535382 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-1183G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535382 | |||||||
chr7:105535405 | T | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-1160T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535405 | |||||||
chr7:105535543 | TTTTG | T | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-1002_89-999delG others(3): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 105535543 | ||||||
chr7:105535753 | G | T | 1 | a0002c0002t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89-812G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105535753 | |||||||
chr7:105536153 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-412C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536153 | |||||||
chr7:105536315 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.89-250C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536315 | |||||||
chr7:105536326 | T | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.89-239T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536326 | |||||||
chr7:105536359 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
16 | HG00544.hp2 HG00621.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-206G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536359 | |||||||
chr7:105536449 | G | A | 5 | a0002c0002t0002g0072 a0002c0002t0002g0094 a0002c0002t0002g0095 others(2): Show |
5 | HG01175.hp2 HG01256.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-116G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536449 | |||||||
chr7:105536449 | G | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-116G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536449 | |||||||
chr7:105536461 | A | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.89-104A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 2/14 | chr7 | 105536461 | |||||||
chr7:105536783 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02257.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.273+34T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105536783 | |||||||
chr7:105536825 | T | C | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.273+76T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105536825 | |||||||
chr7:105536840 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.273+91A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105536840 | |||||||
chr7:105537023 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.273+274T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537023 | |||||||
chr7:105537038 | C | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+289C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537038 | |||||||
chr7:105537125 | A | AT | 11 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(8): Show |
11 | HG00280.hp1 HG01069.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+398dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105537125 | ||||||
chr7:105537125 | AT | A | 16 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0156 others(13): Show |
16 | HG00323.hp1 HG01081.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.273+398delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105537125 | ||||||
chr7:105537125 | ATT | A | 25 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0004t0002g0015 others(22): Show |
26 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.273+397_273+398del others(2): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105537125 | ||||||
chr7:105537125 | ATTT | A | 57 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(54): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.273+396_273+398del others(3): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105537125 | ||||||
chr7:105537125 | ATTTTTTT | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0228 others(4): Show |
8 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+392_273+398del others(7): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105537125 | ||||||
chr7:105537164 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+415C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537164 | |||||||
chr7:105537209 | C | T | 1 | a0002c0002t0002g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.273+460C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537209 | |||||||
chr7:105537376 | T | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+627T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537376 | |||||||
chr7:105537558 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+809G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537558 | |||||||
chr7:105537704 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+955C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537704 | |||||||
chr7:105537768 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.273+1019G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537768 | |||||||
chr7:105537802 | C | G | 1 | a0001c0001t0003g0264 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.273+1053C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537802 | |||||||
chr7:105537831 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01175.hp1 HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.273+1082C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537831 | |||||||
chr7:105537832 | G | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+1083G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537832 | |||||||
chr7:105537865 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0228 others(4): Show |
8 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+1116G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537865 | |||||||
chr7:105537874 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.273+1125T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105537874 | |||||||
chr7:105538363 | T | A | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.273+1614T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538363 | |||||||
chr7:105538372 | G | T | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.273+1623G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538372 | |||||||
chr7:105538471 | T | G | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.273+1722T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538471 | |||||||
chr7:105538670 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.273+1921C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538670 | |||||||
chr7:105538729 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.273+1980T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538729 | |||||||
chr7:105538840 | T | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0107 others(2): Show |
5 | HG00558.hp1 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+2091T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105538840 | |||||||
chr7:105539040 | C | G | 17 | a0001c0001t0003g0011 a0001c0001t0003g0227 a0001c0001t0003g0234 others(14): Show |
20 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.273+2291C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539040 | |||||||
chr7:105539281 | T | C | 1 | a0002c0002t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.273+2532T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539281 | |||||||
chr7:105539285 | C | T | 1 | a0002c0002t0002g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.273+2536C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539285 | |||||||
chr7:105539309 | T | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+2560T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539309 | |||||||
chr7:105539355 | C | CT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | HG00423.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+2628dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105539355 | ||||||
chr7:105539355 | CT | C | 10 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0151 others(7): Show |
10 | HG01069.hp1 HG01168.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.273+2628delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105539355 | ||||||
chr7:105539355 | CTTTTTTT others(3): Show |
C | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.273+2619_273+2628d others(12): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105539355 | ||||||
chr7:105539459 | C | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+2710C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539459 | |||||||
chr7:105539533 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.273+2784T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539533 | |||||||
chr7:105539589 | A | G | 2 | a0002c0006t0002g0030 a0002c0006t0002g0031 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.274-2819A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539589 | |||||||
chr7:105539718 | T | C | 1 | a0002c0002t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-2690T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539718 | |||||||
chr7:105539848 | A | G | 1 | a0002c0003t0002g0069 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274-2560A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539848 | |||||||
chr7:105539937 | C | T | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-2471C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105539937 | |||||||
chr7:105540018 | T | C | 4 | a0002c0006t0002g0027 a0002c0006t0002g0028 a0002c0006t0002g0030 others(1): Show |
4 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-2390T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540018 | |||||||
chr7:105540061 | C | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.274-2347C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540061 | |||||||
chr7:105540074 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.274-2334A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540074 | |||||||
chr7:105540117 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.274-2291C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540117 | |||||||
chr7:105540187 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-2221C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540187 | |||||||
chr7:105540254 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.274-2154A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540254 | |||||||
chr7:105540301 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0256 |
2 | HG02258.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.274-2107C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540301 | |||||||
chr7:105540302 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.274-2106G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540302 | |||||||
chr7:105540307 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.274-2101G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540307 | |||||||
chr7:105540492 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.274-1916C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540492 | |||||||
chr7:105540497 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274-1911A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540497 | |||||||
chr7:105540506 | C | T | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(55): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-1902C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540506 | |||||||
chr7:105540544 | G | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.274-1864G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540544 | |||||||
chr7:105540617 | C | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-1791C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540617 | |||||||
chr7:105540775 | A | C | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.274-1633A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540775 | |||||||
chr7:105540838 | C | CT | 59 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0290 others(56): Show |
65 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.274-1553dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105540838 | ||||||
chr7:105540838 | C | CTT | 29 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(26): Show |
33 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-1554_274-1553d others(4): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105540838 | ||||||
chr7:105540918 | A | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.274-1490A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540918 | |||||||
chr7:105540919 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.274-1489C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540919 | |||||||
chr7:105540971 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0301 |
3 | HG02055.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.274-1437G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540971 | |||||||
chr7:105540980 | G | A | 1 | a0002c0002t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.274-1428G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105540980 | |||||||
chr7:105541131 | C | A | 3 | a0002c0002t0002g0074 a0002c0002t0002g0075 a0002c0002t0002g0076 |
3 | HG01069.hp2 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.274-1277C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541131 | |||||||
chr7:105541152 | T | G | 9 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(6): Show |
13 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-1256T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541152 | |||||||
chr7:105541197 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-1211C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541197 | |||||||
chr7:105541277 | AAGGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0177 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.274-1129_274-1116d others(16): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105541277 | ||||||
chr7:105541379 | C | T | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.274-1029C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541379 | |||||||
chr7:105541415 | G | C | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.274-993G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541415 | |||||||
chr7:105541429 | G | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-979G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541429 | |||||||
chr7:105541552 | C | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-856C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541552 | |||||||
chr7:105541576 | G | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.274-832G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541576 | |||||||
chr7:105541733 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.274-675G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541733 | |||||||
chr7:105541742 | C | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.274-666C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541742 | |||||||
chr7:105541906 | TA | T | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-501delA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541906 | |||||||
chr7:105541997 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01175.hp1 HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.274-411G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105541997 | |||||||
chr7:105542158 | A | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.274-250A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105542158 | |||||||
chr7:105542190 | C | T | 6 | a0002c0003t0002g0007 a0002c0003t0002g0024 a0002c0003t0002g0066 others(3): Show |
8 | HG01243.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-218C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105542190 | |||||||
chr7:105542288 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-120T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105542288 | |||||||
chr7:105542305 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.274-103A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | chr7 | 105542305 | |||||||
chr7:105542387 | CT | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-15delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr7 | 105542387 | ||||||
chr7:105542692 | G | A | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.515+43G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105542692 | |||||||
chr7:105542733 | T | C | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.515+84T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105542733 | |||||||
chr7:105542891 | G | GTCT | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.515+243_515+244ins others(3): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105542891 | ||||||
chr7:105542916 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.515+267C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105542916 | |||||||
chr7:105542977 | C | G | 1 | a0002c0002t0002g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.515+328C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105542977 | |||||||
chr7:105542977 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.515+328C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105542977 | |||||||
chr7:105543127 | C | A | 1 | a0001c0001t0001g0271 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.515+478C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543127 | |||||||
chr7:105543133 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.515+484G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543133 | |||||||
chr7:105543145 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.515+496C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543145 | |||||||
chr7:105543260 | A | C | 6 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0146 others(3): Show |
6 | HG02559.hp2 HG02809.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.515+611A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543260 | |||||||
chr7:105543475 | A | G | 1 | a0002c0006t0002g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.515+826A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543475 | |||||||
chr7:105543968 | C | T | 40 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(37): Show |
42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.515+1319C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105543968 | |||||||
chr7:105544100 | C | CA | 9 | a0001c0001t0001g0158 a0001c0001t0001g0242 a0001c0001t0001g0243 others(6): Show |
9 | HG01106.hp2 HG01192.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.515+1461dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105544100 | ||||||
chr7:105544122 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.515+1473A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544122 | |||||||
chr7:105544259 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.515+1610A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544259 | |||||||
chr7:105544385 | A | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.515+1736A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544385 | |||||||
chr7:105544591 | C | T | 4 | a0002c0003t0002g0026 a0002c0003t0002g0061 a0002c0003t0002g0062 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+1942C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544591 | |||||||
chr7:105544732 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0226 a0001c0001t0001g0266 others(3): Show |
11 | HG00438.hp1 HG02040.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.515+2083G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544732 | |||||||
chr7:105544827 | A | G | 1 | a0002c0006t0002g0029 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.516-2083A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544827 | |||||||
chr7:105544931 | A | G | 1 | a0002c0002t0002g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.516-1979A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544931 | |||||||
chr7:105544937 | A | G | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.516-1973A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105544937 | |||||||
chr7:105545063 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.516-1847A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545063 | |||||||
chr7:105545193 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.516-1717G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545193 | |||||||
chr7:105545197 | T | C | 2 | a0001c0004t0002g0034 a0001c0004t0002g0035 |
2 | NA19003.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.516-1713T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545197 | |||||||
chr7:105545450 | T | TA | 28 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(25): Show |
33 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.516-1446dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105545450 | ||||||
chr7:105545528 | A | AT | 6 | a0001c0001t0002g0005 a0001c0001t0002g0050 a0001c0001t0002g0051 others(3): Show |
10 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-1381dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105545528 | ||||||
chr7:105545530 | A | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0021 others(40): Show |
49 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.516-1380A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545530 | |||||||
chr7:105545530 | AT | A | 32 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(29): Show |
34 | HG00099.hp2 HG00423.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.516-1367delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105545530 | ||||||
chr7:105545531 | T | TA | 7 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0117 others(4): Show |
7 | HG02080.hp2 HG02559.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.516-1379_516-1378i others(3): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545531 | |||||||
chr7:105545532 | T | A | 45 | a0001c0001t0001g0023 a0001c0001t0001g0110 a0001c0001t0001g0114 others(42): Show |
49 | HG00323.hp2 HG00642.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.516-1378T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545532 | |||||||
chr7:105545533 | T | A | 8 | a0002c0002t0002g0072 a0002c0002t0002g0094 a0002c0002t0002g0095 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.516-1377T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545533 | |||||||
chr7:105545534 | T | A | 16 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0004t0002g0036 others(13): Show |
19 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.516-1376T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545534 | |||||||
chr7:105545536 | T | A | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.516-1374T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545536 | |||||||
chr7:105545560 | C | G | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.516-1350C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545560 | |||||||
chr7:105545764 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.516-1146C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545764 | |||||||
chr7:105545889 | C | T | 3 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0262 |
3 | HG01255.hp1 HG02148.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.516-1021C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105545889 | |||||||
chr7:105546005 | A | AG | 11 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0001g0205 others(8): Show |
11 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-898dupG | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 105546005 | ||||||
chr7:105546063 | C | T | 17 | a0001c0001t0001g0293 a0001c0004t0002g0015 a0001c0004t0002g0033 others(14): Show |
18 | HG00558.hp2 HG01943.hp1 HG02922.hp2 others(15): Show |
intron_variant | MODIFIER | c.516-847C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546063 | |||||||
chr7:105546198 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0221 |
2 | HG00140.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.516-712C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546198 | |||||||
chr7:105546222 | C | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG01256.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.516-688C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546222 | |||||||
chr7:105546254 | A | G | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.516-656A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546254 | |||||||
chr7:105546255 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.516-655C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546255 | |||||||
chr7:105546592 | G | A | 26 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(23): Show |
31 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.516-318G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546592 | |||||||
chr7:105546644 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.516-266C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546644 | |||||||
chr7:105546765 | A | G | 1 | a0002c0002t0002g0090 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.516-145A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546765 | |||||||
chr7:105546812 | T | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(109): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.516-98T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546812 | |||||||
chr7:105546814 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0236 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.516-96T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546814 | |||||||
chr7:105546833 | C | G | 1 | a0008c0013t0001g0113 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.516-77C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546833 | |||||||
chr7:105546848 | C | T | 1 | a0002c0002t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.516-62C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546848 | |||||||
chr7:105546852 | G | A | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG01255.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.516-58G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 4/14 | chr7 | 105546852 | |||||||
chr7:105547718 | C | CT | 49 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0201 others(46): Show |
57 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.839+403dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 105547718 | ||||||
chr7:105547718 | C | CTT | 35 | a0001c0004t0002g0045 a0001c0011t0002g0070 a0002c0002t0002g0012 others(32): Show |
37 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.839+402_839+403dup others(2): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 105547718 | ||||||
chr7:105547718 | CT | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(31): Show |
45 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.839+403delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr7 | 105547718 | ||||||
chr7:105547834 | T | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.839+501T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105547834 | |||||||
chr7:105547859 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.839+526C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105547859 | |||||||
chr7:105547872 | C | T | 1 | a0002c0003t0002g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.839+539C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105547872 | |||||||
chr7:105547915 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.839+582C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105547915 | |||||||
chr7:105547943 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.839+610C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105547943 | |||||||
chr7:105548174 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.840-380C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105548174 | |||||||
chr7:105548189 | C | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(82): Show |
95 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.840-365C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105548189 | |||||||
chr7:105548229 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.840-325G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105548229 | |||||||
chr7:105548264 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.840-290G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105548264 | |||||||
chr7:105548283 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.840-271C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 6/14 | chr7 | 105548283 | |||||||
chr7:105548814 | G | T | 1 | a0001c0001t0004g0142 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.996+104G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105548814 | |||||||
chr7:105548891 | T | C | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.996+181T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105548891 | |||||||
chr7:105548939 | T | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.996+229T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105548939 | |||||||
chr7:105549056 | C | G | 6 | a0002c0002t0002g0032 a0002c0006t0002g0027 a0002c0006t0002g0028 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+346C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549056 | |||||||
chr7:105549082 | GGTTCAAG others(354): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.996+401_997-584del | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 105549082 | ||||||
chr7:105549121 | G | A | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.996+411G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549121 | |||||||
chr7:105549122 | G | C | 40 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(37): Show |
42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.996+412G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549122 | |||||||
chr7:105549146 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02257.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.996+436C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549146 | |||||||
chr7:105549241 | C | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(24): Show |
32 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.996+531C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549241 | |||||||
chr7:105549350 | G | A | 3 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0262 |
3 | HG01255.hp1 HG02148.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.996+640G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549350 | |||||||
chr7:105549411 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.997-644T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549411 | |||||||
chr7:105549635 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.997-420T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549635 | |||||||
chr7:105549903 | T | A | 3 | a0002c0003t0002g0016 a0002c0003t0002g0063 a0002c0003t0002g0065 |
4 | HG01074.hp2 HG01884.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-152T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 7/14 | chr7 | 105549903 | |||||||
chr7:105550241 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1108-20A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 8/14 | chr7 | 105550241 | |||||||
chr7:105550675 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1333+189A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105550675 | |||||||
chr7:105550858 | G | C | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1333+372G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105550858 | |||||||
chr7:105550888 | A | G | 109 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(106): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1333+402A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105550888 | |||||||
chr7:105550912 | G | A | 1 | a0002c0003t0002g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1333+426G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105550912 | |||||||
chr7:105550927 | C | A | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1333+441C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105550927 | |||||||
chr7:105551060 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1334-510A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551060 | |||||||
chr7:105551067 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1334-503C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551067 | |||||||
chr7:105551071 | G | A | 5 | a0002c0006t0002g0027 a0002c0006t0002g0028 a0002c0006t0002g0029 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-499G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551071 | |||||||
chr7:105551091 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0137 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1334-479C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551091 | |||||||
chr7:105551261 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1334-309A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551261 | |||||||
chr7:105551339 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1334-231A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551339 | |||||||
chr7:105551382 | G | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(24): Show |
32 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.1334-188G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 9/14 | chr7 | 105551382 | |||||||
chr7:105551717 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0160 others(12): Show |
20 | HG00544.hp2 HG00621.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1471+10T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105551717 | |||||||
chr7:105551846 | G | C | 1 | a0002c0006t0002g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1471+139G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105551846 | |||||||
chr7:105552118 | T | C | 4 | a0002c0002t0002g0072 a0002c0002t0002g0095 a0002c0002t0002g0096 others(1): Show |
4 | HG01256.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1471+411T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552118 | |||||||
chr7:105552347 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0246 |
3 | HG03669.hp1 NA18944.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1471+640G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552347 | |||||||
chr7:105552378 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0117 a0001c0001t0001g0135 others(2): Show |
5 | HG02027.hp2 HG02080.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1471+671A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552378 | |||||||
chr7:105552478 | T | C | 1 | a0002c0005t0002g0081 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1471+771T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552478 | |||||||
chr7:105552604 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0233 a0001c0001t0001g0242 others(17): Show |
21 | HG01106.hp2 HG01169.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1471+897G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552604 | |||||||
chr7:105552666 | C | CT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(52): Show |
69 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1471+984dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552666 | C | CTT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1471+983_1471+984d others(4): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552666 | C | CTTT | 29 | a0001c0001t0001g0023 a0001c0001t0001g0116 a0001c0001t0001g0117 others(26): Show |
30 | HG00642.hp1 HG00642.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1471+982_1471+984d others(5): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552666 | C | CTTTT | 6 | a0001c0001t0001g0104 a0001c0001t0001g0243 a0001c0001t0001g0247 others(3): Show |
6 | HG01169.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1471+981_1471+984d others(6): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552666 | CT | C | 6 | a0001c0001t0001g0267 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01069.hp2 HG01169.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1471+984delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552666 | CTTTTT | C | 32 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0146 others(29): Show |
37 | HG00558.hp2 HG01884.hp1 HG01943.hp1 others(34): Show |
intron_variant | MODIFIER | c.1471+980_1471+984d others(7): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105552666 | ||||||
chr7:105552736 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(135): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1471+1029T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105552736 | |||||||
chr7:105553083 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1471+1376A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553083 | |||||||
chr7:105553194 | AAAG | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1471+1490_1471+149 others(7): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105553194 | ||||||
chr7:105553390 | T | G | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1472-1638T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553390 | |||||||
chr7:105553459 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1472-1569A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553459 | |||||||
chr7:105553589 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1472-1439C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553589 | |||||||
chr7:105553633 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1472-1395G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553633 | |||||||
chr7:105553665 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1472-1363G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553665 | |||||||
chr7:105553686 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1472-1342T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553686 | |||||||
chr7:105553692 | C | G | 4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0285 others(1): Show |
4 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1472-1336C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553692 | |||||||
chr7:105553781 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1472-1247C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553781 | |||||||
chr7:105553790 | G | A | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1472-1238G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553790 | |||||||
chr7:105553887 | A | AT | 37 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0103 others(34): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1472-1112dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105553887 | ||||||
chr7:105553887 | A | ATTTT | 12 | a0002c0002t0002g0012 a0002c0002t0002g0074 a0002c0002t0002g0075 others(9): Show |
13 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1472-1115_1472-111 others(8): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105553887 | ||||||
chr7:105553887 | A | ATTTTT | 15 | a0002c0002t0002g0013 a0002c0002t0002g0072 a0002c0002t0002g0073 others(12): Show |
16 | HG00140.hp1 HG00423.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1472-1116_1472-111 others(9): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105553887 | ||||||
chr7:105553887 | AT | A | 44 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0121 others(41): Show |
54 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1472-1112delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105553887 | ||||||
chr7:105553898 | T | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.1472-1130T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553898 | |||||||
chr7:105553902 | T | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.1472-1126T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553902 | |||||||
chr7:105553975 | C | A | 1 | a0001c0001t0004g0142 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1472-1053C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105553975 | |||||||
chr7:105554133 | C | T | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1472-895C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554133 | |||||||
chr7:105554147 | C | T | 39 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(36): Show |
41 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1472-881C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554147 | |||||||
chr7:105554193 | C | T | 6 | a0001c0001t0001g0172 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1472-835C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554193 | |||||||
chr7:105554269 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1472-759G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554269 | |||||||
chr7:105554323 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0301 |
3 | HG02055.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1472-705G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554323 | |||||||
chr7:105554422 | CTG | C | 33 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(30): Show |
35 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.1472-604_1472-603d others(4): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105554422 | ||||||
chr7:105554437 | C | T | 5 | a0002c0006t0002g0027 a0002c0006t0002g0028 a0002c0006t0002g0029 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1472-591C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554437 | |||||||
chr7:105554441 | C | CT | 6 | a0001c0004t0002g0036 a0001c0004t0002g0037 a0001c0004t0002g0038 others(3): Show |
6 | HG01943.hp1 NA18981.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1472-574dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105554441 | ||||||
chr7:105554441 | CT | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
44 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1472-574delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 105554441 | ||||||
chr7:105554532 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1472-496G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554532 | |||||||
chr7:105554596 | T | C | 68 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(65): Show |
79 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1472-432T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554596 | |||||||
chr7:105554608 | T | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0213 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1472-420T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554608 | |||||||
chr7:105554829 | T | G | 69 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(66): Show |
80 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1472-199T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 10/14 | chr7 | 105554829 | |||||||
chr7:105555269 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1671+42C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105555269 | |||||||
chr7:105555497 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0228 others(4): Show |
8 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1671+270A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105555497 | |||||||
chr7:105555990 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(109): Show |
133 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1671+763A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105555990 | |||||||
chr7:105555998 | A | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(108): Show |
132 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1671+771A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105555998 | |||||||
chr7:105556024 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1671+797T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556024 | |||||||
chr7:105556050 | C | T | 45 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(42): Show |
53 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.1671+823C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556050 | |||||||
chr7:105556069 | CT | C | 9 | a0001c0001t0001g0120 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00438.hp2 NA18522.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671+856delT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105556069 | ||||||
chr7:105556109 | C | T | 5 | a0002c0002t0002g0072 a0002c0002t0002g0094 a0002c0002t0002g0095 others(2): Show |
5 | HG01175.hp2 HG01256.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671+882C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556109 | |||||||
chr7:105556147 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG01891.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671+920A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556147 | |||||||
chr7:105556394 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1671+1167T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556394 | |||||||
chr7:105556524 | T | TA | 41 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(38): Show |
47 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1671+1306dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105556524 | ||||||
chr7:105556533 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1671+1306A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556533 | |||||||
chr7:105556707 | A | AATTATT | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1671+1484_1671+148 others(10): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105556707 | ||||||
chr7:105556728 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.1671+1501G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556728 | |||||||
chr7:105556886 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
44 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1671+1659A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556886 | |||||||
chr7:105556916 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1671+1689T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105556916 | |||||||
chr7:105557145 | G | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1671+1918G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557145 | |||||||
chr7:105557166 | A | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1671+1939A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557166 | |||||||
chr7:105557426 | T | C | 1 | a0002c0006t0002g0029 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1671+2199T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557426 | |||||||
chr7:105557442 | A | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(66): Show |
84 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1671+2215A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557442 | |||||||
chr7:105557554 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1671+2327A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557554 | |||||||
chr7:105557669 | T | C | 1 | a0002c0002t0002g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1671+2442T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105557669 | |||||||
chr7:105558144 | G | A | 37 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0004t0002g0015 others(34): Show |
41 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1671+2917G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558144 | |||||||
chr7:105558293 | C | CA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(80): Show |
106 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1671+3082dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105558293 | ||||||
chr7:105558293 | C | CAA | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(105): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1671+3081_1671+308 others(6): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105558293 | ||||||
chr7:105558293 | CA | C | 31 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0273 others(28): Show |
34 | HG01074.hp2 HG01243.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1671+3082delA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105558293 | ||||||
chr7:105558306 | A | AT | 4 | a0001c0001t0001g0246 a0001c0001t0001g0265 a0001c0001t0003g0139 others(1): Show |
4 | HG02155.hp1 HG02280.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671+3079_1671+308 others(5): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558306 | |||||||
chr7:105558306 | A | T | 19 | a0001c0001t0003g0011 a0001c0001t0003g0138 a0001c0001t0003g0140 others(16): Show |
22 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1671+3079A>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558306 | |||||||
chr7:105558685 | C | T | 2 | a0003c0009t0002g0085 a0003c0009t0002g0089 |
2 | HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1671+3458C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558685 | |||||||
chr7:105558686 | A | G | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1671+3459A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558686 | |||||||
chr7:105558694 | G | A | 1 | a0001c0001t0003g0139 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1671+3467G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558694 | |||||||
chr7:105558796 | C | CATAAA | 133 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(130): Show |
157 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1671+3580_1671+358 others(9): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105558796 | ||||||
chr7:105558797 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1671+3570A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558797 | |||||||
chr7:105558999 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0205 a0001c0001t0001g0219 |
4 | HG00597.hp1 HG00673.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671+3772A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105558999 | |||||||
chr7:105559114 | G | T | 2 | a0001c0004t0002g0015 a0001c0004t0002g0045 |
3 | NA18945.hp1 NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1671+3887G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559114 | |||||||
chr7:105559116 | C | T | 1 | a0002c0002t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1671+3889C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559116 | |||||||
chr7:105559164 | GTGGGTGG others(6): Show |
G | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1671+3940_1671+395 others(17): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559164 | ||||||
chr7:105559209 | A | G | 6 | a0002c0002t0002g0032 a0002c0006t0002g0027 a0002c0006t0002g0028 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671+3982A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559209 | |||||||
chr7:105559223 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(3): Show |
10 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1671+3996C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559223 | |||||||
chr7:105559372 | C | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
44 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1671+4145C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559372 | |||||||
chr7:105559540 | C | CA | 30 | a0001c0001t0001g0167 a0001c0001t0001g0226 a0001c0001t0001g0239 others(27): Show |
34 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1672-4165dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | C | CAA | 12 | a0001c0001t0003g0138 a0001c0001t0003g0141 a0001c0001t0003g0227 others(9): Show |
12 | HG01255.hp1 HG02071.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1672-4166_1672-416 others(6): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | CA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1672-4165delA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | CAA | C | 22 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0001t0001g0254 others(19): Show |
24 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1672-4166_1672-416 others(6): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | CAAAAAA | C | 6 | a0002c0003t0002g0007 a0002c0003t0002g0024 a0002c0003t0002g0066 others(3): Show |
8 | HG01243.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1672-4170_1672-416 others(10): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0006g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1672-4174_1672-416 others(14): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559540 | CAAAAAAA others(5): Show |
C | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1672-4176_1672-416 others(16): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105559540 | ||||||
chr7:105559589 | C | T | 42 | a0001c0001t0003g0011 a0001c0001t0003g0138 a0001c0001t0003g0139 others(39): Show |
48 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1672-4144C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559589 | |||||||
chr7:105559637 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1672-4096C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559637 | |||||||
chr7:105559671 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(99): Show |
120 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1672-4062A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559671 | |||||||
chr7:105559884 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1672-3849C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559884 | |||||||
chr7:105559960 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1672-3773C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559960 | |||||||
chr7:105559992 | G | A | 1 | a0002c0003t0002g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1672-3741G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105559992 | |||||||
chr7:105560060 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1672-3673C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560060 | |||||||
chr7:105560222 | C | T | 36 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0004t0002g0015 others(33): Show |
40 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1672-3511C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560222 | |||||||
chr7:105560312 | A | G | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672-3421A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560312 | |||||||
chr7:105560326 | A | G | 2 | a0004c0008t0001g0185 a0004c0008t0001g0210 |
2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1672-3407A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560326 | |||||||
chr7:105560425 | A | G | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1672-3308A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560425 | |||||||
chr7:105560426 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1672-3307T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560426 | |||||||
chr7:105560456 | C | T | 8 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0002c0002t0002g0032 others(5): Show |
8 | HG01884.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1672-3277C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560456 | |||||||
chr7:105560457 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1672-3276G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560457 | |||||||
chr7:105560476 | G | A | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1672-3257G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560476 | |||||||
chr7:105560654 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1672-3079A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560654 | |||||||
chr7:105560662 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1672-3071A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560662 | |||||||
chr7:105560682 | T | G | 40 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(37): Show |
42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1672-3051T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560682 | |||||||
chr7:105560727 | G | GT | 9 | a0001c0001t0001g0180 a0001c0001t0001g0269 a0001c0001t0001g0272 others(6): Show |
9 | HG00597.hp2 HG02055.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1672-2996dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105560727 | ||||||
chr7:105560774 | G | C | 37 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0004t0002g0015 others(34): Show |
41 | HG00558.hp2 HG01074.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1672-2959G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560774 | |||||||
chr7:105560881 | C | T | 1 | a0002c0006t0002g0030 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1672-2852C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560881 | |||||||
chr7:105560938 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1672-2795C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105560938 | |||||||
chr7:105561009 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1672-2724C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561009 | |||||||
chr7:105561075 | G | A | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1672-2658G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561075 | |||||||
chr7:105561100 | GAAAAA | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(111): Show |
135 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1672-2622_1672-261 others(9): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105561100 | ||||||
chr7:105561141 | C | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0197 a0001c0001t0001g0220 |
3 | NA19009.hp2 NA19080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1672-2592C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561141 | |||||||
chr7:105561176 | T | C | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1672-2557T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561176 | |||||||
chr7:105561211 | C | T | 1 | a0002c0002t0002g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1672-2522C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561211 | |||||||
chr7:105561261 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1672-2472C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561261 | |||||||
chr7:105561500 | C | G | 1 | a0002c0002t0002g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1672-2233C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561500 | |||||||
chr7:105561549 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1672-2184G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561549 | |||||||
chr7:105561557 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2176C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561557 | |||||||
chr7:105561558 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2175A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561558 | |||||||
chr7:105561561 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2172T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561561 | |||||||
chr7:105561566 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2167G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561566 | |||||||
chr7:105561569 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2164G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561569 | |||||||
chr7:105561584 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2149G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561584 | |||||||
chr7:105561597 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1672-2136T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561597 | |||||||
chr7:105561601 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2132G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561601 | |||||||
chr7:105561603 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2130C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561603 | |||||||
chr7:105561613 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1672-2120G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561613 | |||||||
chr7:105561631 | G | A | 1 | a0001c0004t0002g0038 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1672-2102G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561631 | |||||||
chr7:105561840 | G | C | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1672-1893G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561840 | |||||||
chr7:105561858 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1672-1875G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561858 | |||||||
chr7:105561871 | A | AT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0191 a0001c0001t0001g0233 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1672-1854dupT | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105561871 | ||||||
chr7:105561895 | G | A | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672-1838G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561895 | |||||||
chr7:105561951 | A | C | 1 | a0002c0002t0002g0099 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1672-1782A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561951 | |||||||
chr7:105561968 | A | G | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1672-1765A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105561968 | |||||||
chr7:105562134 | G | C | 1 | a0001c0001t0001g0278 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1672-1599G>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562134 | |||||||
chr7:105562170 | C | A | 9 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0115 others(6): Show |
9 | HG01934.hp1 HG02027.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1672-1563C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562170 | |||||||
chr7:105562412 | A | G | 1 | a0001c0001t0003g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1672-1321A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562412 | |||||||
chr7:105562500 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1672-1233G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562500 | |||||||
chr7:105562554 | G | T | 1 | a0001c0004t0002g0033 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1672-1179G>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562554 | |||||||
chr7:105562593 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1672-1140A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562593 | |||||||
chr7:105562620 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1672-1113C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562620 | |||||||
chr7:105562626 | T | C | 1 | a0001c0001t0003g0263 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1672-1107T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562626 | |||||||
chr7:105562637 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1672-1096G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562637 | |||||||
chr7:105562835 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1672-898G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562835 | |||||||
chr7:105562890 | G | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(29): Show |
43 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.1672-843G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562890 | |||||||
chr7:105562982 | T | G | 1 | a0002c0002t0002g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1672-751T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105562982 | |||||||
chr7:105563034 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0197 |
2 | NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1672-699C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563034 | |||||||
chr7:105563066 | T | TA | 40 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0032 others(37): Show |
42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1672-659dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105563066 | ||||||
chr7:105563088 | C | T | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1672-645C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563088 | |||||||
chr7:105563181 | A | C | 34 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0072 others(31): Show |
36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1672-552A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563181 | |||||||
chr7:105563365 | C | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
44 | HG00438.hp1 HG00639.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1672-368C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563365 | |||||||
chr7:105563459 | C | A | 18 | a0002c0003t0002g0007 a0002c0003t0002g0016 a0002c0003t0002g0024 others(15): Show |
21 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1672-274C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563459 | |||||||
chr7:105563627 | C | T | 4 | a0002c0003t0002g0026 a0002c0003t0002g0061 a0002c0003t0002g0062 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1672-106C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | chr7 | 105563627 | |||||||
chr7:105563689 | T | TA | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1672-35dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 105563689 | ||||||
chr7:105564399 | C | G | 1 | a0001c0001t0006g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1886+452C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564399 | |||||||
chr7:105564668 | A | G | 109 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(106): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1887-609A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564668 | |||||||
chr7:105564728 | C | A | 6 | a0002c0002t0002g0032 a0002c0006t0002g0027 a0002c0006t0002g0028 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-549C>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564728 | |||||||
chr7:105564928 | G | A | 11 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0115 others(8): Show |
11 | HG01934.hp1 HG02027.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1887-349G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564928 | |||||||
chr7:105564976 | A | G | 3 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0011t0002g0070 |
3 | HG01884.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1887-301A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564976 | |||||||
chr7:105564981 | A | G | 1 | a0002c0003t0002g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1887-296A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105564981 | |||||||
chr7:105565183 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1887-94C>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105565183 | |||||||
chr7:105565187 | G | A | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.1887-90G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105565187 | |||||||
chr7:105565209 | A | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1887-68A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 12/14 | chr7 | 105565209 | |||||||
chr7:105565463 | T | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG01175.hp1 HG02300.hp1 |
splice_region_variant&intron_variant | LOW | c.2067+6T>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/14 | chr7 | 105565463 | |||||||
chr7:105565470 | A | C | 42 | a0001c0001t0003g0011 a0001c0001t0003g0138 a0001c0001t0003g0139 others(39): Show |
48 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.2067+13A>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/14 | chr7 | 105565470 | |||||||
chr7:105565494 | A | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0048 a0001c0001t0002g0049 others(5): Show |
12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2068-36A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/14 | chr7 | 105565494 | |||||||
chr7:105565508 | T | C | 42 | a0001c0001t0003g0011 a0001c0001t0003g0138 a0001c0001t0003g0139 others(39): Show |
48 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.2068-22T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 13/14 | chr7 | 105565508 | |||||||
chr7:105565760 | T | C | 16 | a0001c0004t0002g0015 a0001c0004t0002g0033 a0001c0004t0002g0034 others(13): Show |
17 | HG00558.hp2 HG01943.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.2186+112T>C | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105565760 | |||||||
chr7:105565925 | G | GAATA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(42): Show |
56 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2186+282_2186+285d others(6): Show |
RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 105565925 | ||||||
chr7:105566007 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2186+359C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566007 | |||||||
chr7:105566023 | A | G | 21 | a0001c0001t0003g0011 a0001c0001t0003g0138 a0001c0001t0003g0139 others(18): Show |
24 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.2186+375A>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566023 | |||||||
chr7:105566113 | AC | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0301 |
3 | HG02055.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2186+467delC | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 105566113 | ||||||
chr7:105566115 | CA | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2186+480delA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 105566115 | ||||||
chr7:105566237 | C | CA | 10 | a0001c0001t0001g0161 a0001c0001t0001g0269 a0001c0001t0002g0005 others(7): Show |
14 | HG02055.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2186+604dupA | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr7 | 105566237 | ||||||
chr7:105566265 | T | G | 1 | a0002c0002t0002g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2186+617T>G | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566265 | |||||||
chr7:105566452 | G | A | 1 | a0001c0001t0003g0303 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2187-667G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566452 | |||||||
chr7:105566595 | G | A | 4 | a0002c0003t0002g0026 a0002c0003t0002g0061 a0002c0003t0002g0062 others(1): Show |
4 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2187-524G>A | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566595 | |||||||
chr7:105566732 | C | T | 1 | a0001c0011t0002g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2187-387C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105566732 | |||||||
chr7:105567090 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2187-29C>T | RINT1 | ENSG00000135249.8 | transcript | ENST00000257700.7 | protein_coding | 14/14 | chr7 | 105567090 |