Item | Value |
---|---|
geneid | 54439 |
ensemblid | ENSG00000091009.8 |
hgncid | 29243 |
symbol | RBM27 |
name | RNA binding motif protein 27 |
refseq_nuc | NM_018989.2 |
refseq_prot | NP_061862.1 |
ensembl_nuc | ENST00000265271.7 |
ensembl_prot | ENSP00000265271.5 |
mane_status | MANE Select |
chr | chr5 |
start | 146203605 |
end | 146289223 |
strand | + |
ver | v1.2 |
region | chr5:146203605-146289223 |
region5000 | chr5:146198605-146294223 |
regionname0 | RBM27_chr5_146203605_146289223 |
regionname5000 | RBM27_chr5_146198605_146294223 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1060 | 270 | 71 | 48 | 106 | 10 | 33 | 84 | RBM27_chr5_146198605_146294223 | RBM27 | MLIED others(1055): Show |
chr5 | 146198605 | 146294223 |
a0002 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | MLIED others(1055): Show |
chr5 | 146198605 | 146294223 |
a0003 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | MLIED others(1055): Show |
chr5 | 146198605 | 146294223 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3180 | 205 | 23 | 40 | 103 | 8 | 29 | RBM27_chr5_146198605_146294223 | RBM27 | ATGCT others(3175): Show |
chr5 | 146198605 | 146294223 | ||
a0001c0002 | 0/0 | 3180 | 62 | 48 | 8 | 0 | 2 | 4 | RBM27_chr5_146198605_146294223 | RBM27 | ATGCT others(3175): Show |
chr5 | 146198605 | 146294223 | ||
a0001c0003 | 0/0 | 3180 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | ATGCT others(3175): Show |
chr5 | 146198605 | 146294223 | ||
a0002c0004 | 0/0 | 3180 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | ATGCT others(3175): Show |
chr5 | 146198605 | 146294223 | ||
a0003c0005 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | ATGCT others(3175): Show |
chr5 | 146198605 | 146294223 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6537 | 98 | 12 | 15 | 48 | 5 | 17 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0002 | 0/1 | 6537 | 70 | 0 | 18 | 39 | 3 | 9 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0006 | 0/0 | 6537 | 7 | 6 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0007 | 0/0 | 6537 | 7 | 0 | 0 | 7 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0008 | 0/0 | 6537 | 4 | 0 | 4 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0010 | 0/0 | 6537 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0011 | 0/0 | 6537 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0017 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0018 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0019 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0020 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0022 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0023 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0025 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0027 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0028 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0029 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0030 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0031 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0001t0032 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0001 | 0/0 | 6537 | 11 | 10 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0003 | 0/0 | 6538 | 17 | 16 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6533): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0004 | 0/0 | 6537 | 15 | 6 | 3 | 0 | 2 | 4 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0005 | 0/0 | 6538 | 8 | 6 | 2 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6533): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0009 | 0/0 | 6537 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0012 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0013 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0014 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0015 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0016 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0021 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0024 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0002t0026 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0001c0003t0002 | 0/0 | 6537 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0002c0004t0004 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
a0003c0005t0012 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | AGTTC others(6532): Show |
chr5 | 146198605 | 146294223 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0010g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0018g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0020g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0022g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0025g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0027g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0028g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0029g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0030g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0031g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0001t0032g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0012g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0021g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0024g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0002t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0002c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
a0003c0005t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0004 | g0025 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0196 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00140 | hp2 | a0001 | c0002 | t0004 | g0019 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0244 | EUR | FIN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00639 | hp2 | a0001 | c0002 | t0004 | g0017 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00735 | hp1 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01069 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0001 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01099 | hp1 | a0001 | c0002 | t0004 | g0023 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01167 | hp1 | a0001 | c0002 | t0012 | g0005 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0131 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0036 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0090 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0108 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01496 | hp1 | a0001 | c0001 | t0020 | g0267 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01884 | hp2 | a0001 | c0002 | t0015 | g0010 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0078 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02040 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02055 | hp2 | a0001 | c0001 | t0029 | g0130 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02135 | hp2 | a0001 | c0003 | t0002 | g0253 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02145 | hp1 | a0001 | c0002 | t0009 | g0009 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0139 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0076 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0136 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02717 | hp1 | a0001 | c0002 | t0024 | g0264 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02717 | hp2 | a0001 | c0002 | t0026 | g0030 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02738 | hp2 | a0001 | c0002 | t0004 | g0016 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02809 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0133 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02896 | hp2 | a0001 | c0002 | t0005 | g0268 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0135 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02970 | hp2 | a0001 | c0001 | t0019 | g0080 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03017 | hp2 | a0001 | c0002 | t0004 | g0022 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03098 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0044 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03209 | hp1 | a0001 | c0002 | t0014 | g0006 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03486 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03491 | hp2 | a0001 | c0002 | t0004 | g0021 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03492 | hp2 | a0001 | c0002 | t0004 | g0024 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03579 | hp1 | a0001 | c0002 | t0016 | g0265 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03579 | hp2 | a0001 | c0002 | t0005 | g0007 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03654 | hp1 | a0001 | c0001 | t0030 | g0171 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03669 | hp1 | a0001 | c0001 | t0018 | g0163 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03831 | hp1 | a0002 | c0004 | t0004 | g0020 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0114 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18522 | hp2 | a0001 | c0002 | t0009 | g0047 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18747 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | CHB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18906 | hp2 | a0003 | c0005 | t0012 | g0046 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18940 | hp2 | a0001 | c0001 | t0017 | g0219 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18942 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18948 | hp1 | a0001 | c0001 | t0025 | g0168 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18949 | hp1 | a0001 | c0001 | t0032 | g0152 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18975 | hp2 | a0001 | c0001 | t0031 | g0245 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18985 | hp1 | a0001 | c0001 | t0010 | g0248 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18989 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18991 | hp1 | a0001 | c0003 | t0002 | g0240 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18991 | hp2 | a0001 | c0001 | t0022 | g0123 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19009 | hp2 | a0001 | c0001 | t0027 | g0146 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | LWK | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19056 | hp1 | a0001 | c0001 | t0010 | g0250 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19079 | hp1 | a0001 | c0001 | t0010 | g0203 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA19240 | hp2 | a0001 | c0002 | t0013 | g0011 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | ASW | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ASW | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0197 | EUR | TSI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | GIH | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | GIH | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02109 | hp2 | a0001 | c0002 | t0021 | g0259 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0137 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02486 | hp2 | a0001 | c0002 | t0009 | g0012 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03471 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0185 | REF | REF | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0066 | REF | REF | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146258493 | A | G | 1 | a0003 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1639A>G | p.Ile547Val | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/21 | 1800/6537 | 1639/3183 | 547/1060 | chr5 | 146258493 | |||
chr5:146285957 | C | A | 1 | a0002 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.3110C>A | p.Thr1037Asn | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3271/6537 | 3110/3183 | 1037/1060 | chr5 | 146285957 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146261779 | T | C | 1 | a0001c0003 | 3 | HG02040.hp1 HG02135.hp2 NA18991.hp1 |
synonymous_variant | LOW | c.2163T>C | p.Pro721Pro | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/21 | 2324/6537 | 2163/3183 | 721/1060 | chr5 | 146261779 | |||
chr5:146271034 | A | G | 3 | a0001c0002 a0002c0004 a0003c0005 |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.2772A>G | p.Lys924Lys | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/21 | 2933/6537 | 2772/3183 | 924/1060 | chr5 | 146271034 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146203696 | G | A | 5 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0013 others(2): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 70 | chr5 | 146203696 | ||||||
chr5:146203706 | T | G | 1 | a0001c0001t0006 | 7 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-60T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 60 | chr5 | 146203706 | ||||||
chr5:146203714 | A | C | 1 | a0001c0001t0032 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 52 | chr5 | 146203714 | ||||||
chr5:146203729 | G | T | 1 | a0001c0001t0031 | 1 | NA18975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 37 | chr5 | 146203729 | ||||||
chr5:146286081 | T | C | 1 | a0001c0002t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 51 | chr5 | 146286081 | ||||||
chr5:146286328 | A | T | 1 | a0001c0001t0008 | 4 | HG01433.hp2 HG01952.hp2 HG01975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*298A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 298 | chr5 | 146286328 | ||||||
chr5:146286354 | T | C | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(2): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 324 | chr5 | 146286354 | ||||||
chr5:146286530 | A | AT | 2 | a0001c0002t0003 a0001c0002t0005 |
25 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*515dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 516 | INFO_REALIGN_3_PRIME | chr5 | 146286530 | |||||
chr5:146286699 | A | G | 1 | a0001c0001t0030 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*669A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 669 | chr5 | 146286699 | ||||||
chr5:146286861 | A | G | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 831 | chr5 | 146286861 | ||||||
chr5:146287042 | A | G | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1012A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1012 | chr5 | 146287042 | ||||||
chr5:146287127 | G | A | 1 | a0001c0001t0018 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1097 | chr5 | 146287127 | ||||||
chr5:146287147 | G | A | 1 | a0001c0001t0019 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1117 | chr5 | 146287147 | ||||||
chr5:146287157 | G | C | 1 | a0001c0002t0013 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1127 | chr5 | 146287157 | ||||||
chr5:146287255 | G | A | 1 | a0001c0001t0007 | 7 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1225G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1225 | chr5 | 146287255 | ||||||
chr5:146287301 | A | G | 1 | a0001c0001t0027 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1271 | chr5 | 146287301 | ||||||
chr5:146287318 | G | A | 1 | a0001c0001t0010 | 3 | NA18985.hp1 NA19056.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1288G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1288 | chr5 | 146287318 | ||||||
chr5:146287461 | A | T | 1 | a0001c0001t0011 | 3 | HG02886.hp1 HG03139.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1431A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1431 | chr5 | 146287461 | ||||||
chr5:146287660 | C | T | 1 | a0001c0002t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1630 | chr5 | 146287660 | ||||||
chr5:146287686 | A | G | 2 | a0001c0002t0013 a0001c0002t0015 |
2 | HG01884.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1656A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1656 | chr5 | 146287686 | ||||||
chr5:146287788 | T | C | 2 | a0001c0002t0004 a0002c0004t0004 |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1758T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1758 | chr5 | 146287788 | ||||||
chr5:146287839 | A | G | 2 | a0001c0002t0004 a0002c0004t0004 |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1809A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1809 | chr5 | 146287839 | ||||||
chr5:146287953 | A | G | 1 | a0001c0001t0025 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1923A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1923 | chr5 | 146287953 | ||||||
chr5:146288296 | A | G | 2 | a0001c0002t0012 a0003c0005t0012 |
2 | HG01167.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2266A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2266 | chr5 | 146288296 | ||||||
chr5:146288478 | C | A | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(3): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2448C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2448 | chr5 | 146288478 | ||||||
chr5:146288516 | C | A | 1 | a0001c0002t0021 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2486C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2486 | chr5 | 146288516 | ||||||
chr5:146288690 | A | G | 1 | a0001c0002t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2660A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2660 | chr5 | 146288690 | ||||||
chr5:146288735 | C | T | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(3): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2705C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2705 | chr5 | 146288735 | ||||||
chr5:146288824 | A | T | 6 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0013 others(3): Show |
15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2794A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2794 | chr5 | 146288824 | ||||||
chr5:146288830 | T | C | 1 | a0001c0001t0017 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2800 | chr5 | 146288830 | ||||||
chr5:146288917 | A | G | 1 | a0001c0001t0023 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2887A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2887 | chr5 | 146288917 | ||||||
chr5:146289060 | A | G | 1 | a0001c0001t0022 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3030A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3030 | chr5 | 146289060 | ||||||
chr5:146289128 | A | G | 1 | a0001c0001t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3098A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3098 | chr5 | 146289128 | ||||||
chr5:146289162 | A | G | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(2): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3132A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3132 | chr5 | 146289162 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:146203845 | C | G | 1 | a0001c0002t0005g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.59+21C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146203845 | |||||||
chr5:146204060 | A | G | 84 | a0001c0001t0001g0004 a0001c0001t0002g0184 a0001c0001t0002g0186 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.59+236A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204060 | |||||||
chr5:146204169 | G | A | 50 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(47): Show |
51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.59+345G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204169 | |||||||
chr5:146204263 | A | G | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+439A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204263 | |||||||
chr5:146204310 | G | A | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+486G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204310 | |||||||
chr5:146204528 | GA | G | 137 | a0001c0001t0001g0004 a0001c0001t0002g0181 a0001c0001t0002g0182 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.59+705delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204528 | |||||||
chr5:146204554 | T | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18982.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.59+730T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204554 | |||||||
chr5:146204573 | A | G | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+749A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204573 | |||||||
chr5:146204630 | G | A | 137 | a0001c0001t0001g0004 a0001c0001t0002g0181 a0001c0001t0002g0182 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.59+806G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204630 | |||||||
chr5:146204767 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+943A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204767 | |||||||
chr5:146204825 | A | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59+1001A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204825 | |||||||
chr5:146204937 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.59+1113T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204937 | |||||||
chr5:146205361 | TAGA | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+1544_59+1546del others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146205361 | ||||||
chr5:146205587 | G | GT | 41 | a0001c0001t0001g0004 a0001c0001t0001g0142 a0001c0001t0001g0143 others(38): Show |
42 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.59+1770dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146205587 | ||||||
chr5:146205628 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.59+1804G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205628 | |||||||
chr5:146205848 | G | A | 10 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2024G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205848 | |||||||
chr5:146205998 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59+2174C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205998 | |||||||
chr5:146206201 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+2377C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206201 | |||||||
chr5:146206247 | T | C | 1 | a0001c0001t0032g0152 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.59+2423T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206247 | |||||||
chr5:146206248 | C | T | 1 | a0001c0001t0032g0152 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.59+2424C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206248 | |||||||
chr5:146206296 | G | T | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+2472G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206296 | |||||||
chr5:146206302 | T | TG | 4 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG01361.hp2 HG03927.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2479dupG | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206302 | ||||||
chr5:146206303 | GT | G | 10 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(7): Show |
10 | HG01167.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2492delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206303 | ||||||
chr5:146206304 | T | G | 127 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(124): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.59+2480T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206304 | |||||||
chr5:146206305 | T | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+2481T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206305 | |||||||
chr5:146206352 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.59+2528T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206352 | |||||||
chr5:146206378 | T | TC | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+2556dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206378 | ||||||
chr5:146206527 | T | A | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+2703T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206527 | |||||||
chr5:146206549 | TA | T | 134 | a0001c0001t0001g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.59+2736delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206549 | ||||||
chr5:146206578 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01257.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.59+2754T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206578 | |||||||
chr5:146206746 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.59+2922A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206746 | |||||||
chr5:146206858 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3034C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206858 | |||||||
chr5:146207010 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59+3186T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207010 | |||||||
chr5:146207315 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59+3491G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207315 | |||||||
chr5:146207454 | T | G | 1 | a0001c0001t0001g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.59+3630T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207454 | |||||||
chr5:146207493 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.59+3669A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207493 | |||||||
chr5:146207502 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.59+3678T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207502 | |||||||
chr5:146207590 | T | TC | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.59+3769dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207590 | ||||||
chr5:146207658 | C | CT | 14 | a0001c0001t0001g0054 a0001c0001t0001g0134 a0001c0001t0001g0178 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.59+3852dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207658 | ||||||
chr5:146207658 | CT | C | 42 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0192 others(39): Show |
43 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.59+3852delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207658 | ||||||
chr5:146207722 | T | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.59+3898T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207722 | |||||||
chr5:146207769 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.59+3945C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207769 | |||||||
chr5:146207903 | C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+4079C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207903 | |||||||
chr5:146207951 | G | GTT | 106 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(103): Show |
107 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.59+4149_59+4150dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | ||||||
chr5:146207951 | G | GTTT | 27 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0249 others(24): Show |
27 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.59+4148_59+4150dup others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | ||||||
chr5:146207951 | G | GTTTT | 5 | a0001c0002t0001g0038 a0001c0002t0003g0036 a0001c0002t0003g0037 others(2): Show |
5 | HG01243.hp1 HG01255.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+4147_59+4150dup others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | ||||||
chr5:146207989 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.59+4165C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207989 | |||||||
chr5:146208017 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.59+4193C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208017 | |||||||
chr5:146208047 | C | T | 2 | a0001c0002t0005g0014 a0001c0002t0005g0015 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.59+4223C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208047 | |||||||
chr5:146208060 | A | C | 5 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0255 others(2): Show |
5 | NA18975.hp2 NA18980.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+4236A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208060 | |||||||
chr5:146208250 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0062 others(6): Show |
9 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+4426G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208250 | |||||||
chr5:146208458 | C | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.59+4634C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208458 | |||||||
chr5:146208486 | G | C | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+4662G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208486 | |||||||
chr5:146208501 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.59+4677C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208501 | |||||||
chr5:146208508 | G | A | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+4684G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208508 | |||||||
chr5:146208683 | T | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59+4859T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208683 | |||||||
chr5:146208920 | G | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.59+5096G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208920 | |||||||
chr5:146209028 | C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+5204C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209028 | |||||||
chr5:146209951 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+6127A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209951 | |||||||
chr5:146209979 | C | T | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.59+6155C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209979 | |||||||
chr5:146210170 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.59+6346T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210170 | |||||||
chr5:146210200 | A | G | 8 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+6376A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210200 | |||||||
chr5:146210322 | A | G | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6498A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210322 | |||||||
chr5:146210331 | A | G | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210331 | |||||||
chr5:146210415 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.59+6591C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210415 | |||||||
chr5:146210589 | C | T | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.59+6765C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210589 | |||||||
chr5:146210674 | A | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+6850A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210674 | |||||||
chr5:146210685 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.59+6861T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210685 | |||||||
chr5:146210686 | G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6862G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210686 | |||||||
chr5:146210863 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59+7039C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210863 | |||||||
chr5:146210878 | C | T | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+7054C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210878 | |||||||
chr5:146211066 | A | G | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.59+7242A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211066 | |||||||
chr5:146211169 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59+7345A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211169 | |||||||
chr5:146211187 | G | A | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+7363G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211187 | |||||||
chr5:146211317 | A | G | 1 | a0001c0002t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59+7493A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211317 | |||||||
chr5:146211464 | C | CT | 29 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0111 others(26): Show |
29 | HG00408.hp1 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.60-7491dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTT | 8 | a0001c0001t0001g0116 a0001c0002t0001g0038 a0001c0002t0003g0035 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-7492_60-7491dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | HG01975.hp1 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.60-7500_60-7491dup others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0251 |
3 | HG01255.hp1 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.60-7501_60-7491dup others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.60-7502_60-7491dup others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.60-7504_60-7491dup others(14): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.60-7506_60-7491dup others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0231 |
3 | HG01257.hp1 HG01496.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.60-7509_60-7491dup others(19): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(13): Show |
9 | a0001c0001t0002g0187 a0001c0001t0002g0196 a0001c0001t0002g0232 others(6): Show |
9 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-7510_60-7491dup others(20): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0238 a0001c0001t0002g0241 a0001c0003t0002g0239 others(2): Show |
5 | HG01981.hp2 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-7511_60-7491dup others(21): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0189 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.60-7512_60-7491dup others(22): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0242 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.60-7514_60-7491dup others(24): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(19): Show |
3 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0254 |
3 | HG00323.hp1 HG00642.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.60-7516_60-7491dup others(26): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0002g0195 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.60-7491_60-7490ins others(31): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | CT | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0067 others(60): Show |
67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.60-7491delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | CTTTTT | C | 41 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(38): Show |
41 | HG00438.hp2 HG02074.hp2 HG02132.hp1 others(38): Show |
intron_variant | MODIFIER | c.60-7495_60-7491del others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | CTTTTTT | C | 16 | a0001c0001t0002g0190 a0001c0001t0002g0197 a0001c0002t0004g0016 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-7496_60-7491del others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-7500_60-7491del others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211464 | CTTTTTTT others(5): Show |
C | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-7502_60-7491del others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | ||||||
chr5:146211494 | T | A | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.60-7491T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211494 | |||||||
chr5:146211574 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.60-7411T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211574 | |||||||
chr5:146211575 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.60-7410G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211575 | |||||||
chr5:146211576 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.60-7409G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211576 | |||||||
chr5:146211680 | C | T | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.60-7305C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211680 | |||||||
chr5:146211717 | GTA | G | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-7267_60-7266del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211717 | |||||||
chr5:146211722 | C | T | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-7263C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211722 | |||||||
chr5:146211856 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.60-7129G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211856 | |||||||
chr5:146212061 | T | TC | 8 | a0001c0001t0001g0054 a0001c0001t0001g0117 a0001c0001t0001g0121 others(5): Show |
8 | HG00741.hp1 HG00741.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-6921dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146212061 | ||||||
chr5:146212202 | C | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-6783C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212202 | |||||||
chr5:146212203 | G | A | 1 | a0001c0002t0009g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.60-6782G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212203 | |||||||
chr5:146212205 | G | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-6780G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212205 | |||||||
chr5:146212300 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0121 |
2 | NA18954.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.60-6685C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212300 | |||||||
chr5:146212301 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.60-6684G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212301 | |||||||
chr5:146212336 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.60-6649G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212336 | |||||||
chr5:146212433 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-6552C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212433 | |||||||
chr5:146212518 | T | A | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60-6467T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212518 | |||||||
chr5:146212594 | T | C | 9 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-6391T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212594 | |||||||
chr5:146212619 | G | C | 1 | a0001c0002t0005g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.60-6366G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212619 | |||||||
chr5:146212731 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-6254A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212731 | |||||||
chr5:146212966 | T | A | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-6019T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212966 | |||||||
chr5:146213082 | G | A | 1 | a0001c0001t0030g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.60-5903G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213082 | |||||||
chr5:146213105 | G | T | 11 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-5880G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213105 | |||||||
chr5:146213225 | C | T | 1 | a0001c0001t0008g0108 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.60-5760C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213225 | |||||||
chr5:146213239 | A | G | 15 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0019 others(12): Show |
15 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.60-5746A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213239 | |||||||
chr5:146213622 | G | A | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-5363G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213622 | |||||||
chr5:146213771 | A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60-5214A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213771 | |||||||
chr5:146214115 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.60-4870C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214115 | |||||||
chr5:146214607 | G | A | 2 | a0001c0001t0007g0057 a0001c0001t0007g0058 |
2 | NA18989.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.60-4378G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214607 | |||||||
chr5:146214652 | T | C | 140 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.60-4333T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214652 | |||||||
chr5:146214675 | A | G | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-4310A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214675 | |||||||
chr5:146214792 | G | A | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-4193G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214792 | |||||||
chr5:146214918 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0140 |
2 | HG02056.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.60-4067C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214918 | |||||||
chr5:146214966 | C | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-4019C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214966 | |||||||
chr5:146215086 | A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60-3899A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215086 | |||||||
chr5:146215088 | C | T | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3897C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215088 | |||||||
chr5:146215130 | A | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0120 |
2 | HG02027.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.60-3855A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215130 | |||||||
chr5:146215164 | C | T | 1 | a0001c0002t0005g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.60-3821C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215164 | |||||||
chr5:146215385 | A | T | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-3600A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215385 | |||||||
chr5:146215440 | A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-3545A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215440 | |||||||
chr5:146215552 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.60-3433T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215552 | |||||||
chr5:146215595 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0107 |
2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.60-3390G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215595 | |||||||
chr5:146215736 | A | C | 2 | a0001c0002t0012g0005 a0003c0005t0012g0046 |
2 | HG01167.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.60-3249A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215736 | |||||||
chr5:146215757 | A | AT | 11 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0002t0001g0038 others(8): Show |
11 | HG01243.hp1 HG01255.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-3215dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146215757 | ||||||
chr5:146215805 | C | T | 1 | a0001c0002t0004g0138 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60-3180C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215805 | |||||||
chr5:146215843 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.60-3142C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215843 | |||||||
chr5:146215939 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.60-3046C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215939 | |||||||
chr5:146215977 | C | G | 2 | a0001c0002t0004g0017 a0001c0002t0004g0026 |
2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.60-3008C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215977 | |||||||
chr5:146216031 | A | C | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.60-2954A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216031 | |||||||
chr5:146216088 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.60-2897G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216088 | |||||||
chr5:146216099 | C | T | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.60-2886C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216099 | |||||||
chr5:146216133 | T | A | 1 | a0001c0001t0002g0229 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.60-2852T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216133 | |||||||
chr5:146216245 | C | T | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.60-2740C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216245 | |||||||
chr5:146216274 | C | T | 1 | a0001c0001t0011g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.60-2711C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216274 | |||||||
chr5:146216511 | G | T | 1 | a0001c0001t0002g0218 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.60-2474G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216511 | |||||||
chr5:146216617 | C | T | 55 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.60-2368C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216617 | |||||||
chr5:146216627 | C | T | 9 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-2358C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216627 | |||||||
chr5:146216653 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60-2332C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216653 | |||||||
chr5:146216657 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60-2328C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216657 | |||||||
chr5:146216768 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.60-2217C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216768 | |||||||
chr5:146217059 | C | T | 1 | a0001c0002t0005g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.60-1926C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217059 | |||||||
chr5:146217069 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.60-1916C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217069 | |||||||
chr5:146217118 | C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-1867C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217118 | |||||||
chr5:146217164 | G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60-1821G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217164 | |||||||
chr5:146217169 | G | C | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-1816G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217169 | |||||||
chr5:146217256 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.60-1729C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217256 | |||||||
chr5:146217262 | C | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-1723C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217262 | |||||||
chr5:146217360 | A | AT | 3 | a0001c0001t0002g0220 a0001c0001t0002g0243 a0001c0001t0002g0244 |
3 | HG00323.hp1 HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.60-1624dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217360 | ||||||
chr5:146217464 | G | GT | 40 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0081 others(37): Show |
40 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.60-1494dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0120 others(5): Show |
8 | HG01243.hp2 HG02027.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-1495_60-1494dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTT | 5 | a0001c0001t0001g0180 a0001c0002t0003g0027 a0001c0002t0003g0031 others(2): Show |
5 | HG02559.hp2 HG02647.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-1496_60-1494dup others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTT | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1497_60-1494dup others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTTTTT others(4): Show |
2 | a0001c0002t0003g0040 a0001c0002t0003g0043 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.60-1504_60-1494dup others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTTTTT others(5): Show |
1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.60-1505_60-1494dup others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTTTTT others(6): Show |
1 | a0001c0002t0003g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60-1506_60-1494dup others(13): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTTTTT others(15): Show |
1 | a0001c0002t0003g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60-1515_60-1494dup others(22): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | G | GTTTTTTT others(21): Show |
1 | a0001c0002t0003g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.60-1494_60-1493ins others(28): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | GT | G | 49 | a0001c0001t0001g0172 a0001c0001t0002g0188 a0001c0001t0002g0189 others(46): Show |
50 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.60-1494delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | GTT | G | 56 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(53): Show |
56 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.60-1495_60-1494del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217464 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.60-1505_60-1494del others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | ||||||
chr5:146217582 | C | G | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.60-1403C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217582 | |||||||
chr5:146217612 | A | T | 1 | a0001c0001t0002g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.60-1373A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217612 | |||||||
chr5:146217614 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.60-1371C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217614 | |||||||
chr5:146217827 | C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60-1158C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217827 | |||||||
chr5:146217828 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.60-1157G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217828 | |||||||
chr5:146217896 | T | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0107 |
2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.60-1089T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217896 | |||||||
chr5:146218054 | A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.60-931A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218054 | |||||||
chr5:146218068 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.60-917C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218068 | |||||||
chr5:146218134 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.60-851A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218134 | |||||||
chr5:146218153 | G | GTA | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-822_60-821dupAT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146218153 | ||||||
chr5:146218212 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-773C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218212 | |||||||
chr5:146218329 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-656T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218329 | |||||||
chr5:146218450 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-535A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218450 | |||||||
chr5:146218521 | C | G | 5 | a0001c0001t0002g0186 a0001c0001t0002g0213 a0001c0001t0002g0216 others(2): Show |
5 | NA18948.hp2 NA18979.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-464C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218521 | |||||||
chr5:146218595 | T | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60-390T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218595 | |||||||
chr5:146218720 | A | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.60-265A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218720 | |||||||
chr5:146219695 | C | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.178+592C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146219695 | |||||||
chr5:146219971 | A | G | 2 | a0001c0002t0003g0028 a0001c0002t0003g0044 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.178+868A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146219971 | |||||||
chr5:146220204 | G | A | 16 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(13): Show |
16 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+1101G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220204 | |||||||
chr5:146220244 | G | A | 3 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0002c0004t0004g0020 |
3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.178+1141G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220244 | |||||||
chr5:146220397 | C | T | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+1294C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220397 | |||||||
chr5:146220461 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.178+1358C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220461 | |||||||
chr5:146220474 | C | CA | 6 | a0001c0001t0001g0117 a0001c0002t0001g0048 a0001c0002t0001g0049 others(3): Show |
6 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+1387dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | ||||||
chr5:146220474 | CA | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(115): Show |
119 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.178+1387delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | ||||||
chr5:146220474 | CAA | C | 6 | a0001c0001t0001g0086 a0001c0002t0005g0001 a0001c0002t0005g0007 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+1386_178+1387d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | ||||||
chr5:146220487 | AAAAT | A | 11 | a0001c0001t0002g0186 a0001c0001t0002g0209 a0001c0001t0002g0210 others(8): Show |
11 | HG00438.hp2 HG02132.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+1386_178+1389d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220487 | ||||||
chr5:146220488 | AAAT | A | 58 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(55): Show |
58 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.178+1387_178+1389d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220488 | ||||||
chr5:146220489 | A | AT | 17 | a0001c0001t0001g0055 a0001c0001t0001g0082 a0001c0001t0001g0087 others(14): Show |
17 | HG00323.hp2 HG01167.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+1386_178+1387i others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220489 | |||||||
chr5:146220489 | A | T | 34 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(31): Show |
36 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.178+1386A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220489 | |||||||
chr5:146220490 | AT | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0011g0003 others(18): Show |
22 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1388delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220490 | |||||||
chr5:146220491 | T | A | 2 | a0001c0002t0003g0031 a0001c0002t0003g0035 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.178+1388T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220491 | |||||||
chr5:146220493 | T | A | 4 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1390T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220493 | |||||||
chr5:146220495 | T | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.178+1392T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220495 | |||||||
chr5:146220497 | T | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178+1394T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220497 | |||||||
chr5:146220501 | T | C | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+1398T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220501 | |||||||
chr5:146220535 | G | A | 7 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+1432G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220535 | |||||||
chr5:146220643 | A | G | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+1540A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220643 | |||||||
chr5:146220872 | G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.178+1769G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220872 | |||||||
chr5:146221093 | C | T | 6 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(3): Show |
6 | HG02109.hp2 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+1990C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221093 | |||||||
chr5:146221127 | G | A | 6 | a0001c0001t0002g0189 a0001c0001t0002g0196 a0001c0001t0002g0230 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+2024G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221127 | |||||||
chr5:146221141 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0019g0080 |
3 | HG02615.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+2038C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221141 | |||||||
chr5:146221147 | C | CA | 9 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2058dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146221147 | ||||||
chr5:146221167 | A | G | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.178+2064A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221167 | |||||||
chr5:146221245 | A | G | 8 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+2142A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221245 | |||||||
chr5:146221520 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.179-1883A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221520 | |||||||
chr5:146221779 | A | G | 12 | a0001c0001t0001g0055 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
12 | HG00323.hp2 HG01099.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-1624A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221779 | |||||||
chr5:146221885 | TATA | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.179-1513_179-1511d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146221885 | ||||||
chr5:146222017 | A | T | 2 | a0001c0002t0004g0021 a0001c0002t0004g0024 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.179-1386A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222017 | |||||||
chr5:146222103 | CT | C | 3 | a0001c0002t0001g0260 a0001c0002t0001g0262 a0001c0002t0001g0263 |
3 | HG02572.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.179-1299delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222103 | |||||||
chr5:146222180 | A | C | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.179-1223A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222180 | |||||||
chr5:146222185 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.179-1218C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222185 | |||||||
chr5:146222216 | G | A | 9 | a0001c0001t0020g0267 a0001c0002t0001g0260 a0001c0002t0001g0261 others(6): Show |
9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-1187G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222216 | |||||||
chr5:146222237 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-1166G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222237 | |||||||
chr5:146222335 | T | C | 55 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-1068T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222335 | |||||||
chr5:146222362 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-1041A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222362 | |||||||
chr5:146222438 | C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.179-965C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222438 | |||||||
chr5:146222453 | G | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0151 |
3 | HG00408.hp2 HG02040.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.179-950G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222453 | |||||||
chr5:146222584 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.179-819C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222584 | |||||||
chr5:146222585 | G | C | 3 | a0001c0001t0006g0126 a0001c0001t0006g0131 a0001c0001t0006g0132 |
3 | HG01243.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.179-818G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222585 | |||||||
chr5:146222590 | A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179-813A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222590 | |||||||
chr5:146222857 | A | T | 6 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-546A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222857 | |||||||
chr5:146222936 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.179-467T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222936 | |||||||
chr5:146222968 | G | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.179-435G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222968 | |||||||
chr5:146223011 | T | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179-392T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223011 | |||||||
chr5:146223169 | C | T | 12 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(9): Show |
12 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-234C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223169 | |||||||
chr5:146223371 | C | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-32C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223371 | |||||||
chr5:146223651 | G | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.303+124G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223651 | |||||||
chr5:146223716 | T | G | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+189T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223716 | |||||||
chr5:146223728 | C | G | 8 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+201C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223728 | |||||||
chr5:146223738 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.303+211T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223738 | |||||||
chr5:146223859 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.303+332T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223859 | |||||||
chr5:146223976 | T | A | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+449T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223976 | |||||||
chr5:146224040 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.303+513A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224040 | |||||||
chr5:146224354 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.303+827G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224354 | |||||||
chr5:146224498 | A | G | 6 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+971A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224498 | |||||||
chr5:146224654 | C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.303+1127C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224654 | |||||||
chr5:146225072 | G | A | 86 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(83): Show |
86 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.303+1545G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225072 | |||||||
chr5:146225092 | C | G | 1 | a0001c0001t0002g0208 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.303+1565C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225092 | |||||||
chr5:146225199 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.303+1672C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225199 | |||||||
chr5:146225567 | G | GT | 14 | a0001c0001t0001g0106 a0001c0001t0002g0188 a0001c0002t0001g0048 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.303+2057dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146225567 | ||||||
chr5:146225567 | GT | G | 69 | a0001c0001t0001g0110 a0001c0001t0001g0128 a0001c0001t0002g0181 others(66): Show |
69 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.303+2057delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146225567 | ||||||
chr5:146225573 | T | G | 2 | a0001c0002t0013g0011 a0001c0002t0015g0010 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.303+2046T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225573 | |||||||
chr5:146225931 | C | T | 55 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.303+2404C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225931 | |||||||
chr5:146226028 | A | ATT | 73 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(70): Show |
73 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.303+2518_303+2519d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146226028 | ||||||
chr5:146226028 | AT | A | 182 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(179): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.303+2519delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146226028 | ||||||
chr5:146226131 | G | T | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+2604G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226131 | |||||||
chr5:146226159 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.303+2632C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226159 | |||||||
chr5:146226707 | T | A | 80 | a0001c0001t0001g0106 a0001c0001t0001g0112 a0001c0001t0001g0140 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.304-2239T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226707 | |||||||
chr5:146226787 | C | G | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304-2159C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226787 | |||||||
chr5:146227029 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-1917A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227029 | |||||||
chr5:146227202 | A | G | 3 | a0001c0002t0009g0012 a0001c0002t0013g0011 a0001c0002t0015g0010 |
3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.304-1744A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227202 | |||||||
chr5:146227429 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.304-1517A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227429 | |||||||
chr5:146227692 | T | G | 1 | a0001c0001t0002g0223 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.304-1254T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227692 | |||||||
chr5:146227710 | A | G | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-1236A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227710 | |||||||
chr5:146227739 | C | A | 86 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(83): Show |
86 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.304-1207C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227739 | |||||||
chr5:146227898 | C | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.304-1048C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227898 | |||||||
chr5:146227909 | C | G | 3 | a0001c0001t0001g0098 a0001c0001t0008g0108 a0001c0001t0023g0114 |
3 | HG01433.hp2 HG01943.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.304-1037C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227909 | |||||||
chr5:146227971 | A | T | 55 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(52): Show |
56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.304-975A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227971 | |||||||
chr5:146227975 | A | G | 7 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-971A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227975 | |||||||
chr5:146228005 | C | T | 34 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(31): Show |
34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.304-941C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228005 | |||||||
chr5:146228257 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.304-689A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228257 | |||||||
chr5:146228278 | C | CT | 6 | a0001c0001t0002g0212 a0001c0001t0002g0257 a0001c0002t0001g0266 others(3): Show |
6 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-665dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228278 | ||||||
chr5:146228280 | TTC | T | 7 | a0001c0002t0001g0038 a0001c0002t0003g0033 a0001c0002t0003g0034 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-664_304-663del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228280 | ||||||
chr5:146228281 | TC | T | 39 | a0001c0001t0002g0199 a0001c0001t0020g0267 a0001c0002t0001g0048 others(36): Show |
40 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.304-664delC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228281 | |||||||
chr5:146228282 | C | T | 95 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.304-664C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228282 | |||||||
chr5:146228316 | G | A | 1 | a0001c0002t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.304-630G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228316 | |||||||
chr5:146228364 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.304-582C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228364 | |||||||
chr5:146228368 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.304-578G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228368 | |||||||
chr5:146228465 | C | T | 1 | a0001c0002t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304-481C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228465 | |||||||
chr5:146228468 | G | A | 6 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-478G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228468 | |||||||
chr5:146228606 | TTTTG | T | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.304-332_304-329del others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228606 | ||||||
chr5:146228625 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.304-321A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228625 | |||||||
chr5:146228732 | C | G | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.304-214C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228732 | |||||||
chr5:146228748 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.304-198G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228748 | |||||||
chr5:146228761 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.304-185T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228761 | |||||||
chr5:146228771 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.304-175A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228771 | |||||||
chr5:146229124 | T | C | 1 | a0001c0001t0006g0075 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.395+87T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 4/20 | chr5 | 146229124 | |||||||
chr5:146229263 | G | T | 11 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0165 others(8): Show |
11 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.395+226G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 4/20 | chr5 | 146229263 | |||||||
chr5:146229977 | G | A | 12 | a0001c0002t0004g0017 a0001c0002t0004g0021 a0001c0002t0004g0022 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+67G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 5/20 | chr5 | 146229977 | |||||||
chr5:146230622 | CTTTGTTT others(7): Show |
C | 3 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0002c0004t0004g0020 |
3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.590-32_590-19delTG others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr5 | 146230622 | ||||||
chr5:146231138 | C | T | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850+221C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231138 | |||||||
chr5:146231356 | C | T | 14 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(11): Show |
14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.850+439C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231356 | |||||||
chr5:146231510 | A | AT | 8 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+601dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr5 | 146231510 | ||||||
chr5:146231763 | G | A | 17 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(14): Show |
17 | HG01978.hp2 HG02132.hp2 HG02976.hp2 others(14): Show |
intron_variant | MODIFIER | c.850+846G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231763 | |||||||
chr5:146232016 | T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.850+1099T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232016 | |||||||
chr5:146232141 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.850+1224G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232141 | |||||||
chr5:146232247 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.851-1203A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232247 | |||||||
chr5:146232360 | A | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.851-1090A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232360 | |||||||
chr5:146232526 | T | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-924T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232526 | |||||||
chr5:146232701 | T | G | 86 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(83): Show |
86 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.851-749T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232701 | |||||||
chr5:146232714 | G | A | 5 | a0001c0001t0002g0188 a0001c0001t0002g0192 a0001c0001t0002g0201 others(2): Show |
5 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-736G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232714 | |||||||
chr5:146232939 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.851-511A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232939 | |||||||
chr5:146233109 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.851-341C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233109 | |||||||
chr5:146233130 | A | G | 1 | a0001c0002t0001g0266 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.851-320A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233130 | |||||||
chr5:146233167 | C | T | 6 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-283C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233167 | |||||||
chr5:146233259 | A | G | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-191A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233259 | |||||||
chr5:146233961 | C | G | 7 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144+218C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146233961 | |||||||
chr5:146234123 | G | A | 6 | a0001c0001t0002g0188 a0001c0001t0002g0192 a0001c0001t0002g0201 others(3): Show |
6 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+380G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234123 | |||||||
chr5:146234280 | T | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1144+537T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234280 | |||||||
chr5:146234472 | T | C | 4 | a0001c0001t0002g0188 a0001c0001t0002g0201 a0001c0001t0002g0207 others(1): Show |
4 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+729T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234472 | |||||||
chr5:146234519 | T | TA | 264 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1144+787dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146234519 | ||||||
chr5:146234631 | G | T | 6 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+888G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234631 | |||||||
chr5:146234813 | C | G | 2 | a0001c0002t0003g0027 a0001c0002t0003g0029 |
2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1144+1070C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234813 | |||||||
chr5:146234854 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1144+1111C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234854 | |||||||
chr5:146235033 | A | AAAAT | 19 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0093 others(16): Show |
19 | HG01167.hp1 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1144+1330_1144+133 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235033 | A | AAAATAAA others(1): Show |
81 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(78): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1144+1326_1144+133 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235033 | A | AAAATAAA others(5): Show |
43 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0062 others(40): Show |
44 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1144+1322_1144+133 others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235033 | A | AAAATAAA others(9): Show |
7 | a0001c0001t0001g0086 a0001c0001t0001g0103 a0001c0001t0001g0157 others(4): Show |
7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+1318_1144+133 others(20): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235033 | AAAAT | A | 36 | a0001c0001t0001g0110 a0001c0001t0002g0190 a0001c0001t0002g0197 others(33): Show |
37 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1144+1330_1144+133 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235033 | AAAATAAA others(1): Show |
A | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1144+1326_1144+133 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | ||||||
chr5:146235077 | A | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0002t0004g0016 others(2): Show |
5 | HG00140.hp2 HG01257.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144+1334A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235077 | |||||||
chr5:146235637 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1145-1661C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235637 | |||||||
chr5:146235655 | T | TA | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1145-1641dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235655 | ||||||
chr5:146235712 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1145-1586C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235712 | |||||||
chr5:146235884 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1145-1414G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235884 | |||||||
chr5:146235922 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-1376C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235922 | |||||||
chr5:146236138 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1160A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236138 | |||||||
chr5:146236139 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1159A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236139 | |||||||
chr5:146236140 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1158G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236140 | |||||||
chr5:146236493 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-805G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236493 | |||||||
chr5:146236930 | C | CT | 13 | a0001c0001t0002g0184 a0001c0001t0002g0191 a0001c0001t0002g0200 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145-344dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146236930 | ||||||
chr5:146236930 | CT | C | 122 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(119): Show |
125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1145-344delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146236930 | ||||||
chr5:146236932 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1145-366T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236932 | |||||||
chr5:146236945 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-353T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236945 | |||||||
chr5:146236954 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1145-344T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236954 | |||||||
chr5:146237024 | C | T | 6 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145-274C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237024 | |||||||
chr5:146237130 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145-168G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237130 | |||||||
chr5:146237220 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1145-78G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237220 | |||||||
chr5:146237591 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1279+159A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146237591 | |||||||
chr5:146238041 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0081 |
2 | HG02257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1279+609G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238041 | |||||||
chr5:146238081 | T | C | 3 | a0001c0001t0006g0002 a0001c0001t0006g0075 a0001c0001t0006g0122 |
4 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+649T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238081 | |||||||
chr5:146238144 | G | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1279+712G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238144 | |||||||
chr5:146238306 | C | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+874C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238306 | |||||||
chr5:146238337 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+905C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238337 | |||||||
chr5:146238534 | C | T | 3 | a0001c0001t0006g0002 a0001c0001t0006g0075 a0001c0001t0006g0122 |
4 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+1102C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238534 | |||||||
chr5:146238569 | T | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1279+1137T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238569 | |||||||
chr5:146238657 | A | AT | 5 | a0001c0001t0001g0121 a0001c0001t0001g0174 a0001c0002t0004g0016 others(2): Show |
5 | HG02717.hp2 HG02738.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+1242dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146238657 | ||||||
chr5:146238657 | AT | A | 92 | a0001c0001t0001g0087 a0001c0001t0002g0181 a0001c0001t0002g0182 others(89): Show |
93 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1279+1242delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146238657 | ||||||
chr5:146239248 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1279+1816C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239248 | |||||||
chr5:146239344 | A | G | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+1912A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239344 | |||||||
chr5:146239467 | C | CTTTTTT | 30 | a0001c0001t0020g0267 a0001c0002t0001g0048 a0001c0002t0001g0049 others(27): Show |
31 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239467 | ||||||
chr5:146239467 | CTTTTCT | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1279+2040_1279+204 others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239467 | ||||||
chr5:146239470 | T | TTTTTTTT others(1): Show |
7 | a0001c0002t0001g0262 a0001c0002t0001g0266 a0001c0002t0003g0027 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239470 | ||||||
chr5:146239471 | T | TTTTTTTC | 25 | a0001c0002t0001g0038 a0001c0002t0001g0260 a0001c0002t0001g0261 others(22): Show |
25 | HG00140.hp2 HG01167.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239471 | |||||||
chr5:146239472 | C | CT | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0164 others(3): Show |
6 | HG01978.hp2 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+2063dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239472 | ||||||
chr5:146239472 | C | T | 34 | a0001c0002t0001g0038 a0001c0002t0001g0260 a0001c0002t0001g0261 others(31): Show |
34 | HG00140.hp2 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1279+2040C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239472 | |||||||
chr5:146239478 | T | C | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+2046T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239478 | |||||||
chr5:146239484 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1279+2052T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239484 | |||||||
chr5:146239620 | G | C | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+2188G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239620 | |||||||
chr5:146239746 | G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+2314G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239746 | |||||||
chr5:146239775 | CT | C | 80 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1279+2362delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239775 | ||||||
chr5:146239874 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+2442C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239874 | |||||||
chr5:146239884 | C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1279+2452C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239884 | |||||||
chr5:146240164 | A | T | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1279+2732A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240164 | |||||||
chr5:146240182 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2750C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240182 | |||||||
chr5:146240290 | T | TTCTG | 43 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0184 others(40): Show |
43 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1279+2861_1279+286 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | ||||||
chr5:146240290 | T | TTCTGTCT others(1): Show |
17 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0192 others(14): Show |
17 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1279+2861_1279+286 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | ||||||
chr5:146240290 | T | TTCTGTCT others(5): Show |
1 | a0001c0001t0002g0258 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1279+2861_1279+286 others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | ||||||
chr5:146240290 | TTCTA | T | 3 | a0001c0001t0002g0220 a0001c0001t0002g0233 a0001c0001t0002g0243 |
3 | HG00642.hp2 HG01192.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1279+2862_1279+286 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | ||||||
chr5:146240294 | A | ATCTG | 12 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0177 others(9): Show |
13 | HG00140.hp2 HG00741.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1279+2898_1279+290 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | ||||||
chr5:146240294 | A | G | 74 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(71): Show |
74 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1279+2862A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240294 | |||||||
chr5:146240294 | ATCTG | A | 39 | a0001c0001t0001g0099 a0001c0001t0001g0156 a0001c0001t0006g0126 others(36): Show |
40 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1279+2898_1279+290 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | ||||||
chr5:146240294 | ATCTGTCT others(1): Show |
A | 5 | a0001c0001t0006g0132 a0001c0002t0004g0136 a0001c0002t0004g0137 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+2894_1279+290 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | ||||||
chr5:146240378 | G | A | 1 | a0001c0001t0007g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1279+2946G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240378 | |||||||
chr5:146240408 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1279+2976C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240408 | |||||||
chr5:146240489 | G | A | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1279+3057G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240489 | |||||||
chr5:146240497 | T | C | 12 | a0001c0002t0004g0017 a0001c0002t0004g0021 a0001c0002t0004g0022 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+3065T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240497 | |||||||
chr5:146240527 | A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+3095A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240527 | |||||||
chr5:146240603 | G | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+3171G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240603 | |||||||
chr5:146240880 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1279+3448G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240880 | |||||||
chr5:146240953 | T | C | 31 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(28): Show |
32 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1279+3521T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240953 | |||||||
chr5:146241164 | TA | T | 63 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1279+3740delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146241164 | ||||||
chr5:146241176 | G | A | 1 | a0001c0002t0004g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1279+3744G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241176 | |||||||
chr5:146241236 | T | A | 6 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279+3804T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241236 | |||||||
chr5:146241507 | A | C | 1 | a0001c0001t0029g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1279+4075A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241507 | |||||||
chr5:146241508 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4076G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241508 | |||||||
chr5:146241530 | A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+4098A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241530 | |||||||
chr5:146241616 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1279+4184G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241616 | |||||||
chr5:146241655 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1279+4223C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241655 | |||||||
chr5:146242135 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4703G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242135 | |||||||
chr5:146242224 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4792C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242224 | |||||||
chr5:146242490 | G | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1279+5058G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242490 | |||||||
chr5:146242501 | C | G | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+5069C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242501 | |||||||
chr5:146242657 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1279+5225G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242657 | |||||||
chr5:146242679 | C | T | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+5247C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242679 | |||||||
chr5:146242720 | A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+5288A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242720 | |||||||
chr5:146242755 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1279+5323G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242755 | |||||||
chr5:146242799 | T | C | 1 | a0001c0001t0002g0254 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1279+5367T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242799 | |||||||
chr5:146242874 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1279+5442A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242874 | |||||||
chr5:146242890 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+5458T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242890 | |||||||
chr5:146242909 | T | C | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+5477T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242909 | |||||||
chr5:146243040 | C | T | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+5608C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243040 | |||||||
chr5:146243170 | G | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+5738G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243170 | |||||||
chr5:146243262 | A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+5830A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243262 | |||||||
chr5:146243458 | T | C | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+6026T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243458 | |||||||
chr5:146243511 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1279+6079A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243511 | |||||||
chr5:146243524 | A | T | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1279+6092A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243524 | |||||||
chr5:146243658 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1279+6226A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243658 | |||||||
chr5:146243721 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1279+6289T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243721 | |||||||
chr5:146243846 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1279+6414T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243846 | |||||||
chr5:146243852 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1279+6420C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243852 | |||||||
chr5:146243902 | T | C | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1279+6470T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243902 | |||||||
chr5:146244083 | A | G | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+6651A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244083 | |||||||
chr5:146244335 | G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+6903G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244335 | |||||||
chr5:146244401 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1279+6969T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244401 | |||||||
chr5:146244640 | G | T | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-7071G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244640 | |||||||
chr5:146244798 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1280-6913C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244798 | |||||||
chr5:146244838 | A | T | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-6873A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244838 | |||||||
chr5:146244909 | T | C | 9 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1280-6802T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244909 | |||||||
chr5:146245109 | C | G | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1280-6602C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245109 | |||||||
chr5:146245409 | C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-6302C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245409 | |||||||
chr5:146245420 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-6291A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245420 | |||||||
chr5:146245924 | G | C | 2 | a0001c0002t0009g0009 a0001c0002t0014g0006 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1280-5787G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245924 | |||||||
chr5:146246073 | CTGTT | C | 7 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-5635_1280-563 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246073 | ||||||
chr5:146246159 | A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1280-5552A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246159 | |||||||
chr5:146246239 | T | C | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1280-5472T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246239 | |||||||
chr5:146246249 | T | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-5462T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246249 | |||||||
chr5:146246313 | A | C | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280-5398A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246313 | |||||||
chr5:146246369 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1280-5342G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246369 | |||||||
chr5:146246749 | G | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0172 a0001c0001t0032g0152 |
3 | NA18949.hp1 NA19063.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1280-4962G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246749 | |||||||
chr5:146246775 | G | A | 7 | a0001c0002t0004g0017 a0001c0002t0004g0021 a0001c0002t0004g0022 others(4): Show |
7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-4936G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246775 | |||||||
chr5:146246864 | G | GT | 11 | a0001c0001t0001g0074 a0001c0001t0002g0214 a0001c0001t0002g0220 others(8): Show |
11 | HG01167.hp1 HG01192.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280-4829dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246864 | ||||||
chr5:146246864 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1280-4847G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246864 | |||||||
chr5:146246864 | GT | G | 7 | a0001c0001t0002g0188 a0001c0001t0002g0192 a0001c0001t0002g0201 others(4): Show |
7 | HG01257.hp1 HG02074.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-4829delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246864 | ||||||
chr5:146246967 | A | G | 3 | a0001c0001t0007g0059 a0001c0001t0007g0060 a0001c0001t0007g0063 |
3 | NA18747.hp2 NA18942.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1280-4744A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246967 | |||||||
chr5:146247011 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1280-4700G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247011 | |||||||
chr5:146247077 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-4634T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247077 | |||||||
chr5:146247250 | T | G | 1 | a0001c0001t0002g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1280-4461T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247250 | |||||||
chr5:146247377 | C | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1280-4334C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247377 | |||||||
chr5:146247379 | T | C | 63 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1280-4332T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247379 | |||||||
chr5:146247548 | G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1280-4163G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247548 | |||||||
chr5:146247739 | C | T | 1 | a0001c0001t0029g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1280-3972C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247739 | |||||||
chr5:146247819 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1280-3892T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247819 | |||||||
chr5:146247943 | A | G | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-3768A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247943 | |||||||
chr5:146248132 | A | G | 34 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(31): Show |
34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1280-3579A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248132 | |||||||
chr5:146248190 | C | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0158 others(4): Show |
7 | HG01257.hp2 HG01981.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-3521C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248190 | |||||||
chr5:146248210 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1280-3501G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248210 | |||||||
chr5:146248234 | G | GT | 129 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1280-3460dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146248234 | ||||||
chr5:146248238 | T | TG | 7 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-3473_1280-347 others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248238 | |||||||
chr5:146248359 | G | A | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1280-3352G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248359 | |||||||
chr5:146248520 | C | T | 3 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 |
3 | NA18944.hp2 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1280-3191C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248520 | |||||||
chr5:146248535 | G | A | 1 | a0001c0002t0001g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1280-3176G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248535 | |||||||
chr5:146248668 | A | G | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1280-3043A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248668 | |||||||
chr5:146248743 | G | A | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1280-2968G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248743 | |||||||
chr5:146248801 | G | T | 2 | a0001c0002t0003g0027 a0001c0002t0003g0029 |
2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1280-2910G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248801 | |||||||
chr5:146248867 | CTTAA | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1280-2840_1280-283 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146248867 | ||||||
chr5:146249130 | C | T | 2 | a0001c0002t0001g0038 a0001c0002t0003g0034 |
2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1280-2581C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249130 | |||||||
chr5:146249184 | T | C | 3 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0015 |
3 | HG02976.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-2527T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249184 | |||||||
chr5:146249204 | A | G | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-2507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249204 | |||||||
chr5:146249231 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1280-2480C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249231 | |||||||
chr5:146249460 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1280-2251T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249460 | |||||||
chr5:146249515 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1280-2196G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249515 | |||||||
chr5:146249547 | C | T | 1 | a0001c0002t0015g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-2164C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249547 | |||||||
chr5:146249574 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-2137C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249574 | |||||||
chr5:146249633 | G | A | 1 | a0001c0001t0007g0063 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1280-2078G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249633 | |||||||
chr5:146249683 | C | CA | 21 | a0001c0001t0002g0188 a0001c0001t0002g0192 a0001c0001t0002g0201 others(18): Show |
21 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1280-2010dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146249683 | ||||||
chr5:146249709 | T | TA | 81 | a0001c0001t0001g0113 a0001c0001t0001g0174 a0001c0001t0002g0181 others(78): Show |
81 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1280-1992dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146249709 | ||||||
chr5:146249822 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1280-1889G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249822 | |||||||
chr5:146249926 | T | G | 1 | a0001c0001t0002g0204 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1280-1785T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249926 | |||||||
chr5:146250004 | T | A | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1280-1707T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250004 | |||||||
chr5:146250040 | C | T | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1280-1671C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250040 | |||||||
chr5:146250041 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1280-1670C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250041 | |||||||
chr5:146250257 | G | A | 56 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(53): Show |
57 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1280-1454G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250257 | |||||||
chr5:146250324 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1280-1387C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250324 | |||||||
chr5:146250431 | C | CA | 115 | a0001c0001t0001g0055 a0001c0001t0001g0068 a0001c0001t0001g0086 others(112): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1280-1262dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250431 | ||||||
chr5:146250431 | C | CAA | 22 | a0001c0001t0002g0198 a0001c0001t0002g0201 a0001c0001t0002g0209 others(19): Show |
22 | HG00438.hp2 HG00741.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1280-1263_1280-126 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250431 | ||||||
chr5:146250757 | T | G | 9 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1280-954T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250757 | |||||||
chr5:146250770 | C | CT | 43 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0101 others(40): Show |
43 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1280-917dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | ||||||
chr5:146250770 | C | CTT | 6 | a0001c0001t0006g0126 a0001c0001t0007g0063 a0001c0002t0001g0266 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-918_1280-917d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | ||||||
chr5:146250770 | CT | C | 92 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0082 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-917delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | ||||||
chr5:146250770 | CTT | C | 6 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-918_1280-917d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | ||||||
chr5:146251053 | GCGTGAGC others(2): Show |
G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1280-647_1280-639d others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146251053 | ||||||
chr5:146251129 | G | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-582G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251129 | |||||||
chr5:146251174 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1280-537T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251174 | |||||||
chr5:146251352 | G | T | 10 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(7): Show |
10 | NA18942.hp2 NA18951.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1280-359G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251352 | |||||||
chr5:146251481 | T | C | 1 | a0001c0002t0003g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1280-230T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251481 | |||||||
chr5:146251489 | C | T | 3 | a0001c0001t0002g0199 a0001c0001t0002g0211 a0001c0001t0002g0218 |
3 | NA18952.hp1 NA18960.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1280-222C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251489 | |||||||
chr5:146251592 | T | G | 1 | a0001c0001t0029g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1280-119T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251592 | |||||||
chr5:146252092 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1444+217A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252092 | |||||||
chr5:146252149 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1444+274T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252149 | |||||||
chr5:146252252 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1444+377C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252252 | |||||||
chr5:146252348 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1444+473C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252348 | |||||||
chr5:146252793 | C | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1444+918C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252793 | |||||||
chr5:146253102 | A | G | 1 | a0001c0002t0009g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1444+1227A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253102 | |||||||
chr5:146253287 | C | T | 9 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0029 others(6): Show |
9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1444+1412C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253287 | |||||||
chr5:146253291 | C | T | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1444+1416C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253291 | |||||||
chr5:146253354 | G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1444+1479G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253354 | |||||||
chr5:146253422 | T | C | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1445-1521T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253422 | |||||||
chr5:146253735 | G | A | 4 | a0001c0002t0004g0136 a0001c0002t0004g0137 a0001c0002t0004g0138 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-1208G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253735 | |||||||
chr5:146253811 | T | C | 1 | a0001c0001t0002g0249 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1445-1132T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253811 | |||||||
chr5:146253911 | T | C | 12 | a0001c0002t0004g0017 a0001c0002t0004g0021 a0001c0002t0004g0022 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1445-1032T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253911 | |||||||
chr5:146254041 | T | A | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1445-902T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254041 | |||||||
chr5:146254143 | G | T | 3 | a0001c0001t0006g0126 a0001c0001t0006g0131 a0001c0001t0006g0132 |
3 | HG01243.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1445-800G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254143 | |||||||
chr5:146254160 | C | CAAAT | 6 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1445-782_1445-779d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254160 | ||||||
chr5:146254431 | AT | A | 89 | a0001c0001t0001g0094 a0001c0001t0002g0181 a0001c0001t0002g0182 others(86): Show |
89 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1445-499delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254431 | ||||||
chr5:146254544 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1445-399A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254544 | |||||||
chr5:146254556 | GA | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-380delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254556 | ||||||
chr5:146254561 | A | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-382A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254561 | |||||||
chr5:146254579 | A | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-364A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254579 | |||||||
chr5:146254639 | C | T | 1 | a0001c0002t0003g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1445-304C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254639 | |||||||
chr5:146254659 | T | G | 1 | a0001c0002t0005g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1445-284T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254659 | |||||||
chr5:146254723 | C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-220C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254723 | |||||||
chr5:146254732 | G | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1445-211G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254732 | |||||||
chr5:146254741 | C | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1445-202C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254741 | |||||||
chr5:146254757 | T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-186T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254757 | |||||||
chr5:146255588 | C | G | 29 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(26): Show |
30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1594+496C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255588 | |||||||
chr5:146255657 | C | A | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+565C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255657 | |||||||
chr5:146255660 | C | G | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+568C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255660 | |||||||
chr5:146255665 | C | G | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+573C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255665 | |||||||
chr5:146255666 | C | A | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+574C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255666 | |||||||
chr5:146255667 | A | T | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+575A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255667 | |||||||
chr5:146255668 | C | G | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+576C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255668 | |||||||
chr5:146255670 | A | T | 1 | a0001c0001t0017g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+578A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255670 | |||||||
chr5:146255710 | G | GT | 4 | a0001c0001t0001g0093 a0001c0001t0001g0109 a0001c0001t0001g0121 others(1): Show |
4 | HG02132.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594+625dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 146255710 | ||||||
chr5:146255852 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1594+760C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255852 | |||||||
chr5:146256056 | A | G | 34 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(31): Show |
34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1594+964A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256056 | |||||||
chr5:146256103 | A | G | 1 | a0001c0002t0004g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1594+1011A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256103 | |||||||
chr5:146256336 | T | A | 1 | a0001c0001t0007g0061 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1594+1244T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256336 | |||||||
chr5:146256357 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1594+1265A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256357 | |||||||
chr5:146256418 | C | T | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1594+1326C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256418 | |||||||
chr5:146256539 | C | T | 1 | a0001c0002t0005g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1594+1447C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256539 | |||||||
chr5:146256872 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1595-1577A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256872 | |||||||
chr5:146257090 | C | T | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1595-1359C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257090 | |||||||
chr5:146257108 | T | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1595-1341T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257108 | |||||||
chr5:146257433 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1595-1016A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257433 | |||||||
chr5:146257489 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1595-960A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257489 | |||||||
chr5:146257506 | C | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(121): Show |
127 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1595-943C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257506 | |||||||
chr5:146257810 | G | GT | 22 | a0001c0001t0001g0160 a0001c0001t0002g0184 a0001c0001t0002g0215 others(19): Show |
23 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595-627dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 146257810 | ||||||
chr5:146258445 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG01346.hp1 | splice_region_variant&intron_variant | LOW | c.1595-4A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146258445 | |||||||
chr5:146258652 | T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1739+59T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146258652 | |||||||
chr5:146258768 | AT | A | 5 | a0001c0001t0001g0062 a0001c0001t0002g0199 a0001c0001t0002g0211 others(2): Show |
5 | HG02273.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1739+191delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146258768 | ||||||
chr5:146258768 | ATT | A | 24 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1739+190_1739+191d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146258768 | ||||||
chr5:146258792 | G | A | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1739+199G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146258792 | |||||||
chr5:146259077 | A | C | 25 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(22): Show |
25 | HG01361.hp1 HG01433.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1739+484A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259077 | |||||||
chr5:146259303 | G | A | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0002g0195 |
3 | HG00639.hp1 HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1739+710G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259303 | |||||||
chr5:146259336 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1739+743A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259336 | |||||||
chr5:146259504 | C | CA | 19 | a0001c0001t0001g0119 a0001c0001t0001g0143 a0001c0001t0001g0147 others(16): Show |
19 | HG01099.hp2 HG01891.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.1739+934dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | ||||||
chr5:146259504 | CA | C | 58 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0094 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1739+934delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | ||||||
chr5:146259504 | CAAAA | C | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1739+931_1739+934d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | ||||||
chr5:146259528 | G | T | 1 | a0001c0001t0002g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1739+935G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259528 | |||||||
chr5:146259546 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1739+953A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259546 | |||||||
chr5:146259740 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1740-1005A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259740 | |||||||
chr5:146259778 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1740-967C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259778 | |||||||
chr5:146259803 | G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1740-942G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259803 | |||||||
chr5:146259836 | A | G | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1740-909A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259836 | |||||||
chr5:146259895 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1740-850C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259895 | |||||||
chr5:146259949 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1740-796C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259949 | |||||||
chr5:146259974 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1740-771C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259974 | |||||||
chr5:146259979 | C | CA | 46 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0068 others(43): Show |
46 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1740-738dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146259979 | C | CAA | 29 | a0001c0001t0001g0054 a0001c0001t0001g0102 a0001c0001t0001g0106 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1740-739_1740-738d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146259979 | C | CAAA | 18 | a0001c0002t0001g0048 a0001c0002t0001g0050 a0001c0002t0001g0262 others(15): Show |
18 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1740-740_1740-738d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146259979 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0095 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1740-752_1740-738d others(17): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146259979 | CAAAA | C | 7 | a0001c0001t0002g0198 a0001c0001t0002g0208 a0001c0001t0002g0225 others(4): Show |
7 | HG00741.hp1 HG01346.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1740-741_1740-738d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146259979 | CAAAAA | C | 69 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(66): Show |
69 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1740-742_1740-738d others(7): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | ||||||
chr5:146260083 | G | A | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1740-662G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260083 | |||||||
chr5:146260086 | G | A | 14 | a0001c0001t0002g0186 a0001c0001t0002g0198 a0001c0001t0002g0209 others(11): Show |
14 | HG00438.hp2 HG02040.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1740-659G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260086 | |||||||
chr5:146260115 | A | T | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1740-630A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260115 | |||||||
chr5:146260268 | C | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1740-477C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260268 | |||||||
chr5:146260293 | C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1740-452C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260293 | |||||||
chr5:146260309 | AAAG | A | 28 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(25): Show |
29 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1740-430_1740-428d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146260309 | ||||||
chr5:146260424 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1740-321A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260424 | |||||||
chr5:146260535 | T | A | 15 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(12): Show |
15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1740-210T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260535 | |||||||
chr5:146260652 | A | G | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1740-93A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260652 | |||||||
chr5:146260719 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1740-26C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260719 | |||||||
chr5:146261120 | A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1893+222A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261120 | |||||||
chr5:146261221 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1894-289G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261221 | |||||||
chr5:146261246 | G | A | 14 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1894-264G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261246 | |||||||
chr5:146261270 | G | A | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1894-240G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261270 | |||||||
chr5:146261294 | C | T | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894-216C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261294 | |||||||
chr5:146261493 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1894-17G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261493 | |||||||
chr5:146261936 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2190+130A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146261936 | |||||||
chr5:146262170 | C | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190+364C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262170 | |||||||
chr5:146262292 | T | TTTG | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2190+488_2190+489i others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262292 | ||||||
chr5:146262444 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2190+638T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262444 | |||||||
chr5:146262445 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2190+639G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262445 | |||||||
chr5:146262544 | C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2190+738C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262544 | |||||||
chr5:146262548 | G | A | 4 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2190+742G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262548 | |||||||
chr5:146262636 | C | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2190+830C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262636 | |||||||
chr5:146262746 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2191-745A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262746 | |||||||
chr5:146262890 | C | CT | 7 | a0001c0002t0001g0260 a0001c0002t0001g0262 a0001c0002t0001g0263 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2191-586dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262890 | ||||||
chr5:146262890 | CT | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0087 a0001c0001t0001g0098 others(2): Show |
5 | HG01099.hp1 HG01433.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-586delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262890 | ||||||
chr5:146262935 | C | G | 1 | a0001c0001t0030g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2191-556C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262935 | |||||||
chr5:146263072 | C | T | 3 | a0001c0002t0004g0016 a0001c0002t0004g0019 a0002c0004t0004g0020 |
3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2191-419C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263072 | |||||||
chr5:146263074 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2191-417G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263074 | |||||||
chr5:146263086 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2191-405G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263086 | |||||||
chr5:146263362 | C | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2191-129C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263362 | |||||||
chr5:146263485 | G | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
splice_region_variant&intron_variant | LOW | c.2191-6G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263485 | |||||||
chr5:146263814 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2331+183T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263814 | |||||||
chr5:146263844 | C | G | 6 | a0001c0001t0002g0215 a0001c0001t0002g0246 a0001c0001t0002g0247 others(3): Show |
6 | HG03688.hp2 NA18975.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.2331+213C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263844 | |||||||
chr5:146263999 | C | T | 7 | a0001c0002t0004g0017 a0001c0002t0004g0021 a0001c0002t0004g0022 others(4): Show |
7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2331+368C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263999 | |||||||
chr5:146264000 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2331+369G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264000 | |||||||
chr5:146264105 | C | CA | 29 | a0001c0001t0001g0100 a0001c0001t0001g0125 a0001c0001t0001g0129 others(26): Show |
29 | HG01167.hp1 HG01243.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.2331+487dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264105 | ||||||
chr5:146264206 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2331+575A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264206 | |||||||
chr5:146264364 | G | A | 3 | a0001c0002t0012g0005 a0001c0002t0026g0030 a0003c0005t0012g0046 |
3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2331+733G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264364 | |||||||
chr5:146264654 | TA | T | 25 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0165 others(22): Show |
26 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2331+1044delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | ||||||
chr5:146264654 | TAA | T | 107 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2331+1043_2331+104 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | ||||||
chr5:146264654 | TAAA | T | 6 | a0001c0001t0020g0267 a0001c0002t0003g0031 a0001c0002t0003g0035 others(3): Show |
6 | HG01496.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2331+1042_2331+104 others(7): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | ||||||
chr5:146264655 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2331+1024A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264655 | |||||||
chr5:146264761 | A | G | 1 | a0001c0002t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2331+1130A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264761 | |||||||
chr5:146264883 | A | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2331+1252A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264883 | |||||||
chr5:146264964 | C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2331+1333C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264964 | |||||||
chr5:146265044 | T | C | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2331+1413T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265044 | |||||||
chr5:146265100 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2331+1469A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265100 | |||||||
chr5:146265159 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2331+1528T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265159 | |||||||
chr5:146265194 | A | G | 1 | a0001c0002t0004g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2331+1563A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265194 | |||||||
chr5:146265266 | G | T | 1 | a0001c0002t0003g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2331+1635G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265266 | |||||||
chr5:146265826 | T | C | 1 | a0001c0002t0004g0135 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2332-1823T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265826 | |||||||
chr5:146265900 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2332-1749C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265900 | |||||||
chr5:146266163 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2332-1486G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266163 | |||||||
chr5:146266187 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0102 |
2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2332-1462C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266187 | |||||||
chr5:146266318 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2332-1331A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266318 | |||||||
chr5:146266808 | G | A | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2332-841G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266808 | |||||||
chr5:146266866 | G | A | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2332-783G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266866 | |||||||
chr5:146267271 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2332-378G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267271 | |||||||
chr5:146267410 | C | A | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2332-239C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267410 | |||||||
chr5:146267588 | C | T | 37 | a0001c0001t0001g0055 a0001c0001t0001g0068 a0001c0001t0001g0070 others(34): Show |
38 | HG00323.hp2 HG01099.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.2332-61C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267588 | |||||||
chr5:146267617 | G | T | 1 | a0001c0001t0022g0123 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2332-32G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267617 | |||||||
chr5:146267930 | AC | A | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2451+163delC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146267930 | |||||||
chr5:146268245 | C | CT | 82 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2451+491dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 146268245 | ||||||
chr5:146268392 | G | A | 2 | a0001c0001t0001g0118 a0001c0002t0026g0030 |
2 | HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2451+624G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268392 | |||||||
chr5:146268702 | C | A | 1 | a0001c0001t0011g0003 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2452-505C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268702 | |||||||
chr5:146268734 | A | G | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2452-473A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268734 | |||||||
chr5:146268740 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2452-467T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268740 | |||||||
chr5:146268782 | C | G | 1 | a0001c0001t0008g0108 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2452-425C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268782 | |||||||
chr5:146268894 | A | C | 5 | a0001c0002t0004g0135 a0001c0002t0004g0136 a0001c0002t0004g0137 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2452-313A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268894 | |||||||
chr5:146269026 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2452-181G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146269026 | |||||||
chr5:146269411 | A | G | 1 | a0001c0003t0002g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2527-9A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 16/20 | chr5 | 146269411 | |||||||
chr5:146269415 | C | T | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.2527-5C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 16/20 | chr5 | 146269415 | |||||||
chr5:146269742 | C | CT | 29 | a0001c0001t0001g0106 a0001c0001t0001g0121 a0001c0001t0001g0156 others(26): Show |
30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2691+182dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | ||||||
chr5:146269742 | C | CTT | 16 | a0001c0002t0003g0039 a0001c0002t0004g0016 a0001c0002t0004g0017 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2691+181_2691+182d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | ||||||
chr5:146269742 | CT | C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0002g0244 others(4): Show |
7 | HG00323.hp1 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2691+182delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | ||||||
chr5:146269742 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2691+172_2691+182d others(13): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | ||||||
chr5:146269772 | A | T | 1 | a0001c0001t0029g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2691+188A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146269772 | |||||||
chr5:146269868 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2691+284C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146269868 | |||||||
chr5:146270002 | C | T | 7 | a0001c0001t0007g0057 a0001c0001t0007g0058 a0001c0001t0007g0059 others(4): Show |
7 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2691+418C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270002 | |||||||
chr5:146270108 | C | G | 63 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2691+524C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270108 | |||||||
chr5:146270329 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2692-625A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270329 | |||||||
chr5:146270337 | TTAC | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2692-616_2692-614d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270337 | |||||||
chr5:146270609 | T | C | 265 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2692-345T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270609 | |||||||
chr5:146270737 | C | T | 2 | a0001c0002t0001g0266 a0001c0002t0016g0265 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2692-217C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270737 | |||||||
chr5:146270821 | A | G | 8 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2692-133A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270821 | |||||||
chr5:146270893 | T | G | 14 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2692-61T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270893 | |||||||
chr5:146271081 | G | A | 3 | a0001c0002t0009g0012 a0001c0002t0013g0011 a0001c0002t0015g0010 |
3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2796+23G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271081 | |||||||
chr5:146271136 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2796+78C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271136 | |||||||
chr5:146271324 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2797-159T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271324 | |||||||
chr5:146271360 | A | G | 4 | a0001c0002t0001g0260 a0001c0002t0001g0262 a0001c0002t0001g0263 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-123A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271360 | |||||||
chr5:146271369 | G | A | 63 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2797-114G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271369 | |||||||
chr5:146271449 | T | C | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2797-34T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271449 | |||||||
chr5:146271903 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2988+229G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146271903 | |||||||
chr5:146271904 | C | T | 14 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2988+230C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146271904 | |||||||
chr5:146272128 | A | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2988+454A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272128 | |||||||
chr5:146272156 | C | G | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2988+482C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272156 | |||||||
chr5:146272416 | T | C | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2988+742T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272416 | |||||||
chr5:146272591 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2988+917G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272591 | |||||||
chr5:146272722 | CA | C | 20 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0094 others(17): Show |
20 | HG01167.hp1 HG01167.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.2988+1063delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146272722 | ||||||
chr5:146273101 | C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2988+1427C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273101 | |||||||
chr5:146273194 | C | T | 1 | a0001c0001t0006g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2988+1520C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273194 | |||||||
chr5:146273290 | A | G | 13 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2988+1616A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273290 | |||||||
chr5:146273369 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+1695T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273369 | |||||||
chr5:146273541 | A | C | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2988+1867A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273541 | |||||||
chr5:146273821 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+2147T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273821 | |||||||
chr5:146273990 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2988+2316T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273990 | |||||||
chr5:146273991 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2988+2317G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273991 | |||||||
chr5:146273995 | T | G | 6 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2988+2321T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273995 | |||||||
chr5:146274217 | T | TA | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2988+2544dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146274217 | ||||||
chr5:146274222 | C | CT | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2988+2559dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146274222 | ||||||
chr5:146274403 | C | T | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2988+2729C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274403 | |||||||
chr5:146274466 | G | T | 1 | a0001c0002t0001g0266 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2988+2792G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274466 | |||||||
chr5:146274608 | T | C | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2988+2934T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274608 | |||||||
chr5:146274644 | T | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2988+2970T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274644 | |||||||
chr5:146274695 | C | A | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2988+3021C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274695 | |||||||
chr5:146274732 | C | T | 3 | a0001c0002t0009g0012 a0001c0002t0013g0011 a0001c0002t0015g0010 |
3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2988+3058C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274732 | |||||||
chr5:146274782 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2988+3108A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274782 | |||||||
chr5:146274789 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2988+3115A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274789 | |||||||
chr5:146275032 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3358T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275032 | |||||||
chr5:146275050 | A | G | 4 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2988+3376A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275050 | |||||||
chr5:146275146 | A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3472A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275146 | |||||||
chr5:146275304 | C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3630C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275304 | |||||||
chr5:146276189 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2988+4515C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276189 | |||||||
chr5:146276414 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2988+4740G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276414 | |||||||
chr5:146276524 | C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+4850C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276524 | |||||||
chr5:146276890 | A | C | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2988+5216A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276890 | |||||||
chr5:146277116 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2988+5442T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277116 | |||||||
chr5:146277181 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2988+5507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277181 | |||||||
chr5:146277212 | C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2988+5538C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277212 | |||||||
chr5:146277241 | T | C | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2988+5567T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277241 | |||||||
chr5:146277359 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2988+5685G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277359 | |||||||
chr5:146277491 | T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2988+5817T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277491 | |||||||
chr5:146277517 | A | AT | 32 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0073 others(29): Show |
33 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2988+5866dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146277517 | ||||||
chr5:146277667 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2988+5993C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277667 | |||||||
chr5:146277735 | T | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2988+6061T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277735 | |||||||
chr5:146277824 | C | T | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2988+6150C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277824 | |||||||
chr5:146277825 | G | A | 2 | a0001c0002t0004g0022 a0001c0002t0004g0023 |
2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2988+6151G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277825 | |||||||
chr5:146277967 | A | G | 7 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2988+6293A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277967 | |||||||
chr5:146278040 | T | C | 91 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(88): Show |
92 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.2988+6366T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278040 | |||||||
chr5:146278089 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2988+6415A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278089 | |||||||
chr5:146278130 | A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+6456A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278130 | |||||||
chr5:146278402 | A | G | 7 | a0001c0002t0001g0038 a0001c0002t0003g0032 a0001c0002t0003g0033 others(4): Show |
7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-6220A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278402 | |||||||
chr5:146278505 | C | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(145): Show |
152 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.2989-6117C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278505 | |||||||
chr5:146278655 | T | C | 3 | a0001c0002t0003g0031 a0001c0002t0003g0035 a0001c0002t0003g0039 |
3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2989-5967T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278655 | |||||||
chr5:146278687 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2989-5935T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278687 | |||||||
chr5:146278869 | T | C | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2989-5753T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278869 | |||||||
chr5:146278885 | C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-5737C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278885 | |||||||
chr5:146279174 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2989-5448G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279174 | |||||||
chr5:146279178 | G | A | 2 | a0001c0002t0012g0005 a0003c0005t0012g0046 |
2 | HG01167.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2989-5444G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279178 | |||||||
chr5:146279231 | C | T | 2 | a0001c0002t0003g0042 a0001c0002t0003g0043 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2989-5391C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279231 | |||||||
chr5:146279235 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2989-5387G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279235 | |||||||
chr5:146279292 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2989-5330A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279292 | |||||||
chr5:146279318 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2989-5304G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279318 | |||||||
chr5:146279452 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2989-5170C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279452 | |||||||
chr5:146279460 | C | CA | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-5152dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146279460 | ||||||
chr5:146279470 | A | C | 1 | a0001c0001t0002g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2989-5152A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279470 | |||||||
chr5:146279562 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2989-5060C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279562 | |||||||
chr5:146279637 | A | G | 14 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2989-4985A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279637 | |||||||
chr5:146279679 | C | T | 16 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2989-4943C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279679 | |||||||
chr5:146279807 | C | CA | 11 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0104 others(8): Show |
11 | HG00642.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.2989-4796dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146279807 | ||||||
chr5:146279860 | T | G | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2989-4762T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279860 | |||||||
chr5:146279982 | G | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2989-4640G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279982 | |||||||
chr5:146280057 | A | AT | 18 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0001t0020g0267 others(15): Show |
18 | HG01167.hp2 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.2989-4551dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146280057 | ||||||
chr5:146280058 | T | A | 1 | a0001c0001t0011g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2989-4564T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280058 | |||||||
chr5:146280092 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2989-4530C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280092 | |||||||
chr5:146280283 | C | T | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2989-4339C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280283 | |||||||
chr5:146280354 | C | T | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2989-4268C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280354 | |||||||
chr5:146280442 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2989-4180C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280442 | |||||||
chr5:146280664 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2989-3958C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280664 | |||||||
chr5:146280850 | T | TTTTA | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2989-3752_2989-374 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146280850 | ||||||
chr5:146280883 | A | G | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2989-3739A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280883 | |||||||
chr5:146280899 | T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-3723T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280899 | |||||||
chr5:146280951 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2989-3671G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280951 | |||||||
chr5:146281017 | C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2989-3605C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281017 | |||||||
chr5:146281134 | C | T | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2989-3488C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281134 | |||||||
chr5:146281142 | C | T | 18 | a0001c0002t0001g0038 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2989-3480C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281142 | |||||||
chr5:146281375 | A | ATGTC | 7 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2989-3245_2989-324 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146281375 | ||||||
chr5:146281817 | G | T | 78 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(75): Show |
78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2989-2805G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281817 | |||||||
chr5:146281986 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2989-2636A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281986 | |||||||
chr5:146282000 | C | CT | 112 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0102 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.2989-2601dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146282000 | ||||||
chr5:146282000 | C | CTT | 32 | a0001c0001t0002g0187 a0001c0001t0002g0201 a0001c0001t0002g0256 others(29): Show |
32 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.2989-2602_2989-260 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146282000 | ||||||
chr5:146282065 | G | A | 14 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0071 others(11): Show |
14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2989-2557G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282065 | |||||||
chr5:146282243 | T | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2989-2379T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282243 | |||||||
chr5:146282249 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2989-2373G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282249 | |||||||
chr5:146282257 | C | T | 63 | a0001c0002t0001g0038 a0001c0002t0001g0048 a0001c0002t0001g0049 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2989-2365C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282257 | |||||||
chr5:146282280 | A | G | 2 | a0001c0002t0004g0021 a0001c0002t0004g0024 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2989-2342A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282280 | |||||||
chr5:146282612 | A | G | 6 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2989-2010A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282612 | |||||||
chr5:146282682 | GACTTGAG others(14): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2989-1939_2989-191 others(25): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282682 | |||||||
chr5:146282862 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2989-1760G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282862 | |||||||
chr5:146282982 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2989-1640T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282982 | |||||||
chr5:146283070 | A | T | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2989-1552A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283070 | |||||||
chr5:146283222 | C | T | 7 | a0001c0002t0009g0009 a0001c0002t0009g0012 a0001c0002t0009g0047 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2989-1400C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283222 | |||||||
chr5:146283478 | A | C | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2989-1144A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283478 | |||||||
chr5:146283690 | C | T | 7 | a0001c0002t0001g0260 a0001c0002t0001g0261 a0001c0002t0001g0262 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-932C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283690 | |||||||
chr5:146283909 | A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-713A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283909 | |||||||
chr5:146283914 | A | G | 7 | a0001c0002t0005g0001 a0001c0002t0005g0007 a0001c0002t0005g0008 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2989-708A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283914 | |||||||
chr5:146284082 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0124 |
2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2989-540G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284082 | |||||||
chr5:146284295 | C | G | 1 | a0001c0001t0002g0236 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2989-327C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284295 | |||||||
chr5:146284296 | C | A | 141 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2989-326C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284296 | |||||||
chr5:146284334 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2989-288G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284334 | |||||||
chr5:146284576 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2989-46G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284576 | |||||||
chr5:146285173 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3099+441C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285173 | |||||||
chr5:146285468 | A | G | 77 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(74): Show |
77 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.3100-479A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285468 | |||||||
chr5:146285560 | T | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3100-387T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285560 | |||||||
chr5:146285582 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3100-365T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285582 | |||||||
chr5:146285791 | C | CT | 38 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0002g0201 others(35): Show |
39 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.3100-142dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr5 | 146285791 | ||||||
chr5:146285791 | C | CTT | 19 | a0001c0002t0003g0028 a0001c0002t0003g0040 a0001c0002t0003g0041 others(16): Show |
19 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3100-143_3100-142d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr5 | 146285791 | ||||||
chr5:146285815 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3100-132G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285815 |