Item | Value |
---|---|
geneid | 10267 |
ensemblid | ENSG00000132329.11 |
hgncid | 9843 |
symbol | RAMP1 |
name | receptor activity modifying protein 1 |
refseq_nuc | NM_005855.4 |
refseq_prot | NP_005846.1 |
ensembl_nuc | ENST00000254661.5 |
ensembl_prot | ENSP00000254661.4 |
mane_status | MANE Select |
chr | chr2 |
start | 237859623 |
end | 237912106 |
strand | + |
ver | v1.2 |
region | chr2:237859623-237912106 |
region5000 | chr2:237854623-237917106 |
regionname0 | RAMP1_chr2_237859623_237912106 |
regionname5000 | RAMP1_chr2_237854623_237917106 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 148 | 403 | 98 | 74 | 168 | 17 | 44 | 122 | RAMP1_chr2_237854623_237917106 | RAMP1 | MARAL others(143): Show |
chr2 | 237854623 | 237917106 |
a0002 | 0/0 | 148 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | MARAL others(143): Show |
chr2 | 237854623 | 237917106 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 444 | 339 | 95 | 67 | 118 | 16 | 41 | RAMP1_chr2_237854623_237917106 | RAMP1 | ATGGC others(439): Show |
chr2 | 237854623 | 237917106 | ||
a0001c0002 | 0/0 | 444 | 63 | 3 | 7 | 50 | 0 | 3 | RAMP1_chr2_237854623_237917106 | RAMP1 | ATGGC others(439): Show |
chr2 | 237854623 | 237917106 | ||
a0001c0004 | 0/0 | 444 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | ATGGC others(439): Show |
chr2 | 237854623 | 237917106 | ||
a0002c0003 | 0/0 | 444 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | ATGGC others(439): Show |
chr2 | 237854623 | 237917106 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 823 | 326 | 84 | 67 | 117 | 16 | 40 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0001t0002 | 0/0 | 823 | 6 | 5 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0001t0003 | 0/0 | 823 | 5 | 5 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0001t0004 | 0/0 | 823 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0001t0006 | 0/0 | 823 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0002t0001 | 0/0 | 823 | 63 | 3 | 7 | 50 | 0 | 3 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0001c0004t0005 | 0/0 | 823 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
a0002c0003t0001 | 0/0 | 823 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | AGTCC others(818): Show |
chr2 | 237854623 | 237917106 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0001g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0002t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0001c0004t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0202 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0376 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0391 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0348 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0347 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0390 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0388 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0367 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0370 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0335 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0386 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0383 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0394 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0342 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0393 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0392 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0313 | SAS | PJL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0351 | SAS | BEB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0361 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0379 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0382 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0375 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0389 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0358 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0385 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0373 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0381 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0377 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0395 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0387 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0378 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0371 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0384 | AFR | ASW | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20752 | hp1 | a0001 | c0004 | t0005 | g0178 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | GIH | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0333 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0197 | REF | REF | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0094 | REF | REF | RAMP1_chr2_237854623_237917106 | RAMP1 | chr2 | 237854623 | 237917106 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237877268 | G | A | 1 | a0002 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.97G>A | p.Gly33Ser | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/3 | 150/823 | 97/447 | 33/148 | chr2 | 237877268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237859681 | C | T | 1 | a0001c0002 | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
synonymous_variant | LOW | c.6C>T | p.Ala2Ala | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/3 | 59/823 | 6/447 | 2/148 | chr2 | 237859681 | |||
chr2:237859723 | C | T | 1 | a0001c0002 | 63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
synonymous_variant | LOW | c.48C>T | p.Leu16Leu | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/3 | 101/823 | 48/447 | 16/148 | chr2 | 237859723 | |||
chr2:237911708 | G | A | 1 | a0001c0004 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.372G>A | p.Val124Val | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 425/823 | 372/447 | 124/148 | chr2 | 237911708 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237911786 | G | C | 1 | a0001c0001t0004 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 3 | chr2 | 237911786 | ||||||
chr2:237911893 | C | G | 1 | a0001c0001t0002 | 6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*110C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 110 | chr2 | 237911893 | ||||||
chr2:237912005 | C | T | 1 | a0001c0001t0003 | 5 | HG02717.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*222C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 222 | chr2 | 237912005 | ||||||
chr2:237912030 | G | C | 1 | a0001c0004t0005 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 247 | chr2 | 237912030 | ||||||
chr2:237912099 | T | C | 1 | a0001c0001t0006 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 3/3 | 316 | chr2 | 237912099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:237859797 | G | GGGGAGCG others(3): Show |
1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+94_52+103dupAGC others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237859797 | ||||||
chr2:237859797 | GGGGAGCG others(3): Show |
G | 69 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(66): Show |
69 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.52+94_52+103delAGC others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237859797 | ||||||
chr2:237859806 | G | A | 12 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0147 others(9): Show |
12 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+79G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859806 | |||||||
chr2:237859818 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.52+91G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859818 | |||||||
chr2:237859821 | A | G | 6 | a0001c0001t0001g0390 a0001c0001t0001g0391 a0001c0001t0001g0392 others(3): Show |
6 | HG01109.hp2 HG01993.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+94A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859821 | |||||||
chr2:237859856 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+129C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859856 | |||||||
chr2:237859861 | C | T | 5 | a0001c0002t0001g0385 a0001c0002t0001g0386 a0001c0002t0001g0387 others(2): Show |
5 | HG02004.hp1 HG02300.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+134C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859861 | |||||||
chr2:237859924 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.52+197C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859924 | |||||||
chr2:237859944 | C | T | 2 | a0001c0002t0001g0383 a0001c0002t0001g0384 |
2 | HG02698.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.52+217C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237859944 | |||||||
chr2:237860109 | G | A | 1 | a0001c0002t0001g0321 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.52+382G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860109 | |||||||
chr2:237860147 | C | G | 63 | a0001c0002t0001g0321 a0001c0002t0001g0328 a0001c0002t0001g0329 others(60): Show |
63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+420C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860147 | |||||||
chr2:237860417 | C | T | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.52+690C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860417 | |||||||
chr2:237860456 | G | A | 63 | a0001c0002t0001g0321 a0001c0002t0001g0328 a0001c0002t0001g0329 others(60): Show |
63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+729G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860456 | |||||||
chr2:237860471 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0002g0316 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52+744A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860471 | |||||||
chr2:237860616 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52+889C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860616 | |||||||
chr2:237860685 | G | GTGT | 90 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0228 others(87): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.52+959_52+961dupTG others(1): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237860685 | ||||||
chr2:237860718 | C | G | 1 | a0001c0001t0006g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52+991C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860718 | |||||||
chr2:237860732 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.52+1005G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860732 | |||||||
chr2:237860734 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.52+1007A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860734 | |||||||
chr2:237860799 | T | C | 64 | a0001c0001t0001g0013 a0001c0002t0001g0321 a0001c0002t0001g0328 others(61): Show |
64 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.52+1072T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860799 | |||||||
chr2:237860823 | G | A | 1 | a0001c0001t0001g0390 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+1096G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860823 | |||||||
chr2:237860862 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02559.hp2 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.52+1135A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237860862 | |||||||
chr2:237860888 | AGATCTGC others(18): Show |
A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+1165_52+1189del others(25): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237860888 | ||||||
chr2:237861037 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
200 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.52+1310A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861037 | |||||||
chr2:237861041 | A | C | 63 | a0001c0002t0001g0321 a0001c0002t0001g0328 a0001c0002t0001g0329 others(60): Show |
63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1314A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861041 | |||||||
chr2:237861047 | A | T | 1 | a0001c0001t0001g0320 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+1320A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861047 | |||||||
chr2:237861218 | G | A | 63 | a0001c0002t0001g0321 a0001c0002t0001g0328 a0001c0002t0001g0329 others(60): Show |
63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1491G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861218 | |||||||
chr2:237861249 | A | G | 63 | a0001c0002t0001g0321 a0001c0002t0001g0328 a0001c0002t0001g0329 others(60): Show |
63 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.52+1522A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861249 | |||||||
chr2:237861347 | A | C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+1620A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861347 | |||||||
chr2:237861422 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(9): Show |
13 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+1695C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861422 | |||||||
chr2:237861583 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.52+1856C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861583 | |||||||
chr2:237861705 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(32): Show |
36 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+1978G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861705 | |||||||
chr2:237861706 | G | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(32): Show |
36 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.52+1979G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861706 | |||||||
chr2:237861812 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0004g0127 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52+2085C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861812 | |||||||
chr2:237861835 | G | A | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+2108G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861835 | |||||||
chr2:237861851 | C | CA | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
139 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.52+2138dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237861851 | ||||||
chr2:237861972 | G | A | 1 | a0001c0001t0001g0390 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+2245G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237861972 | |||||||
chr2:237862103 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+2376C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862103 | |||||||
chr2:237862173 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.52+2446T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862173 | |||||||
chr2:237862185 | G | A | 1 | a0001c0002t0001g0385 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.52+2458G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862185 | |||||||
chr2:237862244 | G | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG01993.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+2517G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862244 | |||||||
chr2:237862402 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+2675C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862402 | |||||||
chr2:237862504 | G | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(9): Show |
13 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+2777G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862504 | |||||||
chr2:237862541 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+2814C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862541 | |||||||
chr2:237862553 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52+2826C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862553 | |||||||
chr2:237862667 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+2940C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862667 | |||||||
chr2:237862763 | C | T | 1 | a0001c0002t0001g0381 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.52+3036C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862763 | |||||||
chr2:237862774 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
163 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+3047T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862774 | |||||||
chr2:237862822 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.52+3095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862822 | |||||||
chr2:237862886 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.52+3159G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862886 | |||||||
chr2:237862919 | A | G | 3 | a0001c0001t0001g0312 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | NA19066.hp1 NA19074.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.52+3192A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862919 | |||||||
chr2:237862932 | T | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(80): Show |
84 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.52+3205T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237862932 | |||||||
chr2:237863000 | T | C | 68 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
68 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.52+3273T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863000 | |||||||
chr2:237863008 | A | G | 2 | a0001c0002t0001g0379 a0001c0002t0001g0380 |
2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.52+3281A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863008 | |||||||
chr2:237863013 | A | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3286A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863013 | |||||||
chr2:237863194 | AGGGGACA others(9): Show |
A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
37 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.52+3471_52+3486del others(16): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237863194 | ||||||
chr2:237863226 | T | C | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+3499T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863226 | |||||||
chr2:237863441 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3714T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863441 | |||||||
chr2:237863481 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+3754A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863481 | |||||||
chr2:237863502 | C | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.52+3775C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863502 | |||||||
chr2:237863540 | T | C | 16 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(13): Show |
16 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.52+3813T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863540 | |||||||
chr2:237863550 | A | G | 1 | a0001c0002t0001g0388 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52+3823A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863550 | |||||||
chr2:237863595 | A | T | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+3868A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863595 | |||||||
chr2:237863748 | G | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(15): Show |
19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4021G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863748 | |||||||
chr2:237863751 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+4024C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863751 | |||||||
chr2:237863752 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(15): Show |
19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4025C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863752 | |||||||
chr2:237863758 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(15): Show |
19 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.52+4031T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863758 | |||||||
chr2:237863761 | A | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
137 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+4034A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863761 | |||||||
chr2:237863814 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0395 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.52+4087C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863814 | |||||||
chr2:237863877 | GC | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0323 a0001c0001t0001g0324 others(4): Show |
7 | HG01993.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+4154delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237863877 | ||||||
chr2:237863893 | G | C | 136 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
137 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.52+4166G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863893 | |||||||
chr2:237863970 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.52+4243C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237863970 | |||||||
chr2:237864086 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
155 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.52+4359A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864086 | |||||||
chr2:237864145 | ACCTGGCC others(5): Show |
A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0395 a0001c0001t0003g0223 |
3 | HG02717.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.52+4424_52+4435del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864145 | ||||||
chr2:237864151 | CCCGTGGC others(5): Show |
C | 25 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(22): Show |
25 | HG01099.hp2 HG01175.hp2 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+4427_52+4438del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864151 | ||||||
chr2:237864273 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.52+4546C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864273 | |||||||
chr2:237864303 | TGCCCAAC others(7): Show |
T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4578_52+4591del others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864303 | ||||||
chr2:237864316 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0323 a0001c0001t0001g0324 others(3): Show |
6 | HG02809.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+4589G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864316 | |||||||
chr2:237864336 | CTGCCGCT others(1): Show |
C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4611_52+4618del others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864336 | ||||||
chr2:237864345 | T | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4618T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864345 | |||||||
chr2:237864347 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0119 others(17): Show |
21 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+4620A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864347 | |||||||
chr2:237864399 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(136): Show |
141 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.52+4672T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864399 | |||||||
chr2:237864404 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(134): Show |
139 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.52+4677T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864404 | |||||||
chr2:237864430 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(135): Show |
140 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.52+4703G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864430 | |||||||
chr2:237864437 | T | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(11): Show |
14 | HG01099.hp2 HG01175.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+4710T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864437 | |||||||
chr2:237864611 | G | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(139): Show |
144 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.52+4884G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864611 | |||||||
chr2:237864631 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.52+4904C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864631 | |||||||
chr2:237864664 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.52+4937T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864664 | |||||||
chr2:237864795 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0002g0186 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.52+5068G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864795 | |||||||
chr2:237864888 | C | CTT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(137): Show |
142 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.52+5163_52+5164dup others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237864888 | ||||||
chr2:237864954 | G | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0121 a0001c0001t0001g0122 others(30): Show |
34 | HG01099.hp2 HG01175.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.52+5227G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237864954 | |||||||
chr2:237865009 | G | T | 2 | a0001c0001t0001g0394 a0001c0001t0002g0214 |
2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+5282G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865009 | |||||||
chr2:237865062 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(56): Show |
61 | HG00438.hp2 HG00741.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.52+5335A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865062 | |||||||
chr2:237865301 | A | G | 11 | a0001c0001t0001g0129 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG01884.hp2 HG01993.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+5574A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865301 | |||||||
chr2:237865487 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0110 others(36): Show |
41 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.52+5760A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865487 | |||||||
chr2:237865549 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG00423.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.52+5822C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865549 | |||||||
chr2:237865635 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+5908A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865635 | |||||||
chr2:237865685 | C | T | 82 | a0001c0001t0001g0109 a0001c0001t0001g0129 a0001c0001t0001g0133 others(79): Show |
82 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(79): Show |
intron_variant | MODIFIER | c.52+5958C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865685 | |||||||
chr2:237865725 | G | A | 3 | a0001c0001t0001g0390 a0001c0001t0001g0394 a0001c0001t0002g0214 |
3 | HG01884.hp2 HG01993.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.52+5998G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865725 | |||||||
chr2:237865732 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.52+6005C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865732 | |||||||
chr2:237865814 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.52+6087C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865814 | |||||||
chr2:237865871 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.52+6144G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865871 | |||||||
chr2:237865895 | C | T | 56 | a0001c0001t0001g0115 a0001c0002t0001g0321 a0001c0002t0001g0328 others(53): Show |
56 | HG00558.hp1 HG00639.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.52+6168C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865895 | |||||||
chr2:237865946 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.52+6219G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237865946 | |||||||
chr2:237866116 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.52+6389G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866116 | |||||||
chr2:237866120 | C | T | 1 | a0001c0002t0001g0377 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.52+6393C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866120 | |||||||
chr2:237866132 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52+6405G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866132 | |||||||
chr2:237866176 | A | T | 1 | a0001c0002t0001g0387 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.52+6449A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866176 | |||||||
chr2:237866500 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+6773G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866500 | |||||||
chr2:237866545 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52+6818A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866545 | |||||||
chr2:237866565 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+6838G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866565 | |||||||
chr2:237866588 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+6861C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866588 | |||||||
chr2:237866589 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+6862A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866589 | |||||||
chr2:237866605 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.52+6878G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866605 | |||||||
chr2:237866636 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01168.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.52+6909C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866636 | |||||||
chr2:237866726 | CT | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0110 others(59): Show |
64 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.52+7011delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237866726 | ||||||
chr2:237866738 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7011T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866738 | |||||||
chr2:237866739 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7012C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866739 | |||||||
chr2:237866763 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.52+7036C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866763 | |||||||
chr2:237866815 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.52+7088A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866815 | |||||||
chr2:237866822 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.52+7095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866822 | |||||||
chr2:237866890 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.52+7163G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866890 | |||||||
chr2:237866996 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.52+7269T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237866996 | |||||||
chr2:237867050 | A | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(18): Show |
23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.52+7323A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867050 | |||||||
chr2:237867118 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+7391C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867118 | |||||||
chr2:237867162 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+7435G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867162 | |||||||
chr2:237867304 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.52+7577G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867304 | |||||||
chr2:237867413 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.52+7686T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867413 | |||||||
chr2:237867430 | C | T | 75 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0001g0157 others(72): Show |
75 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(72): Show |
intron_variant | MODIFIER | c.52+7703C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867430 | |||||||
chr2:237867477 | T | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0110 others(27): Show |
32 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.52+7750T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867477 | |||||||
chr2:237867526 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0296 |
2 | HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.52+7799C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867526 | |||||||
chr2:237867629 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+7902A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867629 | |||||||
chr2:237867634 | C | T | 23 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0131 others(20): Show |
23 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.52+7907C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867634 | |||||||
chr2:237867678 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52+7951C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867678 | |||||||
chr2:237867752 | C | T | 10 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG01175.hp2 HG02074.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+8025C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867752 | |||||||
chr2:237867788 | G | C | 70 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(67): Show |
70 | HG00609.hp1 HG00639.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.52+8061G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867788 | |||||||
chr2:237867852 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.52+8125A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867852 | |||||||
chr2:237867888 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.52+8161A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237867888 | |||||||
chr2:237868046 | C | CT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG01884.hp1 HG01993.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+8335dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868046 | ||||||
chr2:237868093 | G | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(19): Show |
24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.52+8366G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868093 | |||||||
chr2:237868278 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02559.hp2 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.52+8551C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868278 | |||||||
chr2:237868477 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-8747G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868477 | |||||||
chr2:237868495 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(19): Show |
24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-8729G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868495 | |||||||
chr2:237868568 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8656T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868568 | |||||||
chr2:237868569 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8655C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868569 | |||||||
chr2:237868575 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8649A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868575 | |||||||
chr2:237868577 | C | CA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0122 a0001c0001t0001g0130 others(3): Show |
6 | HG02055.hp2 HG03225.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8635dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868577 | ||||||
chr2:237868585 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8639A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868585 | |||||||
chr2:237868589 | AC | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0196 a0001c0002t0001g0335 others(3): Show |
6 | HG01109.hp1 HG02165.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8634delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868589 | |||||||
chr2:237868590 | C | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-8634C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868590 | |||||||
chr2:237868590 | CAA | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
173 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(170): Show |
intron_variant | MODIFIER | c.53-8622_53-8621del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868590 | ||||||
chr2:237868590 | CAAA | C | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-8623_53-8621del others(3): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868590 | ||||||
chr2:237868591 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8633A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868591 | |||||||
chr2:237868592 | A | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0196 a0001c0002t0001g0335 others(3): Show |
6 | HG01109.hp1 HG02165.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8632A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868592 | |||||||
chr2:237868593 | A | C | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.53-8631A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868593 | |||||||
chr2:237868594 | A | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG00733.hp2 NA18979.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.53-8630A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868594 | |||||||
chr2:237868595 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8629A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868595 | |||||||
chr2:237868617 | T | G | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
12 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-8607T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868617 | |||||||
chr2:237868674 | C | T | 9 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(6): Show |
9 | NA18941.hp2 NA18950.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-8550C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868674 | |||||||
chr2:237868701 | TGCTTGGC others(1): Show |
T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-8515_53-8508del others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237868701 | ||||||
chr2:237868813 | G | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(19): Show |
24 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-8411G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868813 | |||||||
chr2:237868899 | G | A | 1 | a0001c0001t0006g0313 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.53-8325G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868899 | |||||||
chr2:237868901 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-8323C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868901 | |||||||
chr2:237868989 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-8235C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237868989 | |||||||
chr2:237869011 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0189 a0001c0001t0001g0190 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8213G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869011 | |||||||
chr2:237869111 | ACCCTGCA others(140): Show |
A | 1 | a0001c0002t0001g0334 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.53-8112_53-7966del | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869111 | |||||||
chr2:237869115 | T | G | 1 | a0001c0002t0001g0333 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53-8109T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869115 | |||||||
chr2:237869205 | C | G | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0110 others(38): Show |
43 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.53-8019C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869205 | |||||||
chr2:237869319 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-7905T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869319 | |||||||
chr2:237869341 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.53-7883T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869341 | |||||||
chr2:237869353 | C | T | 22 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0131 others(19): Show |
22 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.53-7871C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869353 | |||||||
chr2:237869775 | C | G | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
12 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-7449C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869775 | |||||||
chr2:237869839 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
10 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-7385G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869839 | |||||||
chr2:237869861 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-7363C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869861 | |||||||
chr2:237869889 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02080.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.53-7335C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869889 | |||||||
chr2:237869907 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-7317G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237869907 | |||||||
chr2:237870101 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-7123G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870101 | |||||||
chr2:237870297 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(42): Show |
47 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.53-6927G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870297 | |||||||
chr2:237870407 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.53-6817C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870407 | |||||||
chr2:237870427 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.53-6797G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870427 | |||||||
chr2:237870442 | A | G | 23 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0131 others(20): Show |
23 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6782A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870442 | |||||||
chr2:237870512 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-6712C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870512 | |||||||
chr2:237870589 | C | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(18): Show |
23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6635C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870589 | |||||||
chr2:237870598 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(46): Show |
51 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.53-6626T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870598 | |||||||
chr2:237870660 | G | A | 1 | a0001c0002t0001g0341 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.53-6564G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870660 | |||||||
chr2:237870891 | A | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(82): Show |
87 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.53-6333A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870891 | |||||||
chr2:237870893 | C | A | 1 | a0001c0001t0001g0395 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-6331C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870893 | |||||||
chr2:237870942 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-6282G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237870942 | |||||||
chr2:237871040 | C | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0099 others(39): Show |
44 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.53-6184C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871040 | |||||||
chr2:237871041 | G | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(18): Show |
23 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-6183G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871041 | |||||||
chr2:237871097 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.53-6127G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871097 | |||||||
chr2:237871116 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.53-6108G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871116 | |||||||
chr2:237871302 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53-5922C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871302 | |||||||
chr2:237871430 | C | G | 1 | a0001c0001t0003g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.53-5794C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871430 | |||||||
chr2:237871500 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0132 others(9): Show |
12 | HG01099.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.53-5724T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871500 | |||||||
chr2:237871570 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0003g0021 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.53-5654G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871570 | |||||||
chr2:237871593 | G | GC | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG00544.hp1 HG02071.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5625dupC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237871593 | ||||||
chr2:237871648 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG03239.hp1 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5576G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871648 | |||||||
chr2:237871674 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
200 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(197): Show |
intron_variant | MODIFIER | c.53-5550C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871674 | |||||||
chr2:237871697 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.53-5527G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871697 | |||||||
chr2:237871758 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.53-5466G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237871758 | |||||||
chr2:237872031 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5193G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872031 | |||||||
chr2:237872208 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(105): Show |
110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.53-5016G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872208 | |||||||
chr2:237872217 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-5007C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872217 | |||||||
chr2:237872233 | T | C | 1 | a0001c0001t0001g0390 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.53-4991T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872233 | |||||||
chr2:237872256 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4968G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872256 | |||||||
chr2:237872267 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.53-4957G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872267 | |||||||
chr2:237872267 | G | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4957G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872267 | |||||||
chr2:237872302 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53-4922G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872302 | |||||||
chr2:237872320 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.53-4904A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872320 | |||||||
chr2:237872363 | G | A | 59 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0297 others(56): Show |
59 | HG00639.hp2 HG01109.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.53-4861G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872363 | |||||||
chr2:237872431 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0004g0127 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53-4793C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872431 | |||||||
chr2:237872602 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4622G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872602 | |||||||
chr2:237872611 | G | C | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0110 others(38): Show |
43 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.53-4613G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872611 | |||||||
chr2:237872710 | G | A | 145 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(142): Show |
147 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.53-4514G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872710 | |||||||
chr2:237872740 | A | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0238 others(8): Show |
12 | HG00597.hp2 HG00673.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-4484A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872740 | |||||||
chr2:237872755 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.53-4469T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872755 | |||||||
chr2:237872765 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-4459G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872765 | |||||||
chr2:237872781 | CTGTGGGA others(6): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.53-4442_53-4430del others(13): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872781 | |||||||
chr2:237872803 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.53-4421G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872803 | |||||||
chr2:237872886 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.53-4338G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872886 | |||||||
chr2:237872908 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-4316T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872908 | |||||||
chr2:237872910 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-4314C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872910 | |||||||
chr2:237872914 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.53-4310G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237872914 | |||||||
chr2:237873198 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-4026C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873198 | |||||||
chr2:237873308 | G | C | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-3916G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873308 | |||||||
chr2:237873355 | T | A | 1 | a0001c0001t0001g0394 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-3869T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873355 | |||||||
chr2:237873419 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-3805G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873419 | |||||||
chr2:237873426 | C | T | 1 | a0001c0001t0004g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-3798C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873426 | |||||||
chr2:237873462 | G | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0224 a0001c0001t0003g0126 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3762G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873462 | |||||||
chr2:237873508 | C | T | 61 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0093 others(58): Show |
61 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.53-3716C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873508 | |||||||
chr2:237873551 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0233 a0001c0001t0001g0395 |
3 | HG02818.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.53-3673T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873551 | |||||||
chr2:237873553 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0233 a0001c0001t0001g0395 |
3 | HG02818.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.53-3671A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873553 | |||||||
chr2:237873587 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0093 others(8): Show |
11 | HG02055.hp2 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-3637G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873587 | |||||||
chr2:237873595 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0170 a0001c0001t0001g0224 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3629T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873595 | |||||||
chr2:237873620 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0224 a0001c0001t0001g0233 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3604T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873620 | |||||||
chr2:237873630 | G | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0224 a0001c0001t0001g0233 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3594G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237873630 | |||||||
chr2:237874067 | A | G | 1 | a0001c0002t0001g0376 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-3157A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874067 | |||||||
chr2:237874173 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-3051T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874173 | |||||||
chr2:237874320 | G | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0172 a0001c0001t0001g0210 others(2): Show |
5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-2904G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874320 | |||||||
chr2:237874330 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53-2894C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874330 | |||||||
chr2:237874338 | G | C | 38 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(35): Show |
38 | HG00544.hp1 HG01099.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.53-2886G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874338 | |||||||
chr2:237874406 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
4 | NA18950.hp2 NA18954.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-2818C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874406 | |||||||
chr2:237874469 | C | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0187 a0001c0001t0001g0224 others(5): Show |
8 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-2755C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874469 | |||||||
chr2:237874514 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(19): Show |
24 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-2710G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874514 | |||||||
chr2:237874531 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(19): Show |
24 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-2693G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874531 | |||||||
chr2:237874596 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG02280.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.53-2628G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874596 | |||||||
chr2:237874620 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0224 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.53-2604C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874620 | |||||||
chr2:237874664 | G | A | 1 | a0001c0002t0001g0382 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.53-2560G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874664 | |||||||
chr2:237874677 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0189 |
2 | HG01099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.53-2547C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874677 | |||||||
chr2:237874884 | TA | T | 42 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00544.hp1 HG01099.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.53-2338delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237874884 | ||||||
chr2:237874924 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.53-2300C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874924 | |||||||
chr2:237874943 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.53-2281C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237874943 | |||||||
chr2:237875116 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(89): Show |
94 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.53-2108C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875116 | |||||||
chr2:237875227 | G | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(85): Show |
90 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.53-1997G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875227 | |||||||
chr2:237875228 | G | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0172 a0001c0001t0001g0210 others(2): Show |
5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-1996G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875228 | |||||||
chr2:237875257 | A | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(107): Show |
112 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.53-1967A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875257 | |||||||
chr2:237875266 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-1958G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875266 | |||||||
chr2:237875393 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1831G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875393 | |||||||
chr2:237875395 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1829A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875395 | |||||||
chr2:237875404 | TTCTGCCC others(30): Show |
T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02109.hp1 HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.53-1815_53-1779del others(37): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 237875404 | ||||||
chr2:237875425 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(111): Show |
118 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.53-1799A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875425 | |||||||
chr2:237875486 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG02280.hp1 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-1738G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875486 | |||||||
chr2:237875488 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0039 |
3 | HG01256.hp1 HG01975.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.53-1736G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875488 | |||||||
chr2:237875519 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0204 a0001c0001t0002g0118 |
3 | HG01891.hp2 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-1705G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875519 | |||||||
chr2:237875526 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(89): Show |
96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.53-1698T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875526 | |||||||
chr2:237875530 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(115): Show |
122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.53-1694G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875530 | |||||||
chr2:237875651 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
121 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.53-1573A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875651 | |||||||
chr2:237875680 | T | C | 5 | a0001c0001t0001g0129 a0001c0001t0001g0172 a0001c0001t0001g0210 others(2): Show |
5 | HG00642.hp2 HG01346.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-1544T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875680 | |||||||
chr2:237875682 | G | GA | 3 | a0001c0002t0001g0328 a0001c0002t0001g0359 a0001c0002t0001g0360 |
3 | HG02027.hp1 HG02155.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.53-1542_53-1541ins others(1): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875682 | |||||||
chr2:237875683 | C | G | 3 | a0001c0002t0001g0328 a0001c0002t0001g0359 a0001c0002t0001g0360 |
3 | HG02027.hp1 HG02155.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.53-1541C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875683 | |||||||
chr2:237875692 | C | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1532C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875692 | |||||||
chr2:237875724 | A | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(113): Show |
120 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.53-1500A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875724 | |||||||
chr2:237875821 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.53-1403C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875821 | |||||||
chr2:237875875 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.53-1349C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237875875 | |||||||
chr2:237876030 | T | G | 24 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(21): Show |
24 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-1194T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876030 | |||||||
chr2:237876041 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-1183G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876041 | |||||||
chr2:237876105 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0003g0223 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.53-1119C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876105 | |||||||
chr2:237876108 | C | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-1116C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876108 | |||||||
chr2:237876134 | G | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18961.hp2 NA18962.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.53-1090G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876134 | |||||||
chr2:237876194 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-1030G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876194 | |||||||
chr2:237876343 | G | A | 1 | a0001c0002t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53-881G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876343 | |||||||
chr2:237876372 | G | T | 1 | a0001c0002t0001g0372 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.53-852G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876372 | |||||||
chr2:237876424 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(67): Show |
74 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.53-800G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876424 | |||||||
chr2:237876590 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.53-634C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876590 | |||||||
chr2:237876607 | G | A | 18 | a0001c0001t0001g0121 a0001c0001t0001g0133 a0001c0001t0001g0134 others(15): Show |
18 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.53-617G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876607 | |||||||
chr2:237876608 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.53-616C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876608 | |||||||
chr2:237876631 | C | T | 1 | a0001c0002t0001g0387 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.53-593C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876631 | |||||||
chr2:237876644 | G | A | 23 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(20): Show |
23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-580G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876644 | |||||||
chr2:237876652 | CG | C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(20): Show |
23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-571delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876652 | |||||||
chr2:237876656 | C | G | 23 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(20): Show |
23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-568C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876656 | |||||||
chr2:237876658 | C | A | 23 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(20): Show |
23 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-566C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876658 | |||||||
chr2:237876709 | C | T | 1 | a0001c0002t0001g0371 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876709 | |||||||
chr2:237876752 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.53-472C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876752 | |||||||
chr2:237876786 | G | T | 1 | a0001c0002t0001g0371 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.53-438G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876786 | |||||||
chr2:237876797 | C | T | 1 | a0001c0001t0001g0395 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.53-427C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876797 | |||||||
chr2:237876817 | G | T | 25 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(22): Show |
25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-407G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876817 | |||||||
chr2:237876849 | C | G | 6 | a0001c0002t0001g0341 a0001c0002t0001g0354 a0001c0002t0001g0355 others(3): Show |
6 | NA18950.hp1 NA18975.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-375C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876849 | |||||||
chr2:237876861 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.53-363G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876861 | |||||||
chr2:237876876 | T | G | 1 | a0001c0001t0001g0042 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.53-348T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876876 | |||||||
chr2:237876904 | C | A | 6 | a0001c0002t0001g0346 a0001c0002t0001g0347 a0001c0002t0001g0348 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-320C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876904 | |||||||
chr2:237876956 | A | G | 25 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(22): Show |
25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-268A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876956 | |||||||
chr2:237876978 | T | A | 25 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(22): Show |
25 | HG01099.hp1 HG01175.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-246T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237876978 | |||||||
chr2:237877000 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.53-224C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877000 | |||||||
chr2:237877001 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-223G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877001 | |||||||
chr2:237877018 | C | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(41): Show |
46 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.53-206C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877018 | |||||||
chr2:237877095 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-129G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877095 | |||||||
chr2:237877130 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-94G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877130 | |||||||
chr2:237877133 | G | A | 1 | a0001c0004t0005g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.53-91G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877133 | |||||||
chr2:237877154 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.53-70G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877154 | |||||||
chr2:237877189 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.53-35C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877189 | |||||||
chr2:237877190 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.53-34G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877190 | |||||||
chr2:237877210 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0003g0126 a0001c0001t0004g0127 |
3 | HG00280.hp1 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53-14C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 1/2 | chr2 | 237877210 | |||||||
chr2:237877372 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.191+10A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877372 | |||||||
chr2:237877395 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.191+33G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877395 | |||||||
chr2:237877397 | T | C | 2 | a0001c0002t0001g0379 a0001c0002t0001g0380 |
2 | NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.191+35T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877397 | |||||||
chr2:237877490 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+128G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877490 | |||||||
chr2:237877490 | G | T | 134 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0018 others(131): Show |
135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.191+128G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877490 | |||||||
chr2:237877494 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.191+132G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877494 | |||||||
chr2:237877561 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(19): Show |
24 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.191+199G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877561 | |||||||
chr2:237877631 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191+269C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877631 | |||||||
chr2:237877851 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.191+489G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877851 | |||||||
chr2:237877873 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.191+511A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877873 | |||||||
chr2:237877881 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0390 |
2 | HG01993.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.191+519C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237877881 | |||||||
chr2:237878018 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+656G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878018 | |||||||
chr2:237878082 | C | T | 21 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(18): Show |
21 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.191+720C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878082 | |||||||
chr2:237878230 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.191+868G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878230 | |||||||
chr2:237878417 | T | G | 10 | a0001c0001t0001g0116 a0001c0002t0001g0361 a0001c0002t0001g0375 others(7): Show |
10 | HG02004.hp1 HG02300.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+1055T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878417 | |||||||
chr2:237878518 | G | A | 2 | a0001c0001t0003g0126 a0001c0001t0004g0127 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+1156G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878518 | |||||||
chr2:237878605 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(117): Show |
124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.191+1243C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878605 | |||||||
chr2:237878635 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+1273T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878635 | |||||||
chr2:237878793 | G | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+1431G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878793 | |||||||
chr2:237878870 | G | T | 2 | a0001c0001t0001g0260 a0001c0002t0001g0334 |
2 | NA19003.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.191+1508G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878870 | |||||||
chr2:237878892 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+1530C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237878892 | |||||||
chr2:237879049 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.191+1687A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879049 | |||||||
chr2:237879266 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+1904G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879266 | |||||||
chr2:237879415 | C | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(7): Show |
10 | HG00642.hp2 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.191+2053C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879415 | |||||||
chr2:237879449 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191+2087C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879449 | |||||||
chr2:237879479 | C | T | 2 | a0001c0002t0001g0377 a0001c0002t0001g0387 |
2 | NA19011.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.191+2117C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879479 | |||||||
chr2:237879482 | TTTTTTA | T | 20 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(17): Show |
20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2123_191+2128d others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879482 | ||||||
chr2:237879485 | T | C | 27 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): Show |
27 | HG00544.hp1 HG00642.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.191+2123T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879485 | |||||||
chr2:237879488 | A | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0394 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.191+2126A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879488 | |||||||
chr2:237879491 | A | C | 20 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(17): Show |
20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2129A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879491 | |||||||
chr2:237879502 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+2140T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879502 | |||||||
chr2:237879537 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0210 others(3): Show |
6 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+2175C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879537 | |||||||
chr2:237879584 | C | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2222C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879584 | |||||||
chr2:237879594 | C | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2232C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879594 | |||||||
chr2:237879596 | C | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2234C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879596 | |||||||
chr2:237879597 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2235G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879597 | |||||||
chr2:237879598 | T | C | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2236T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879598 | |||||||
chr2:237879599 | C | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2237C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879599 | |||||||
chr2:237879601 | T | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2239T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879601 | |||||||
chr2:237879611 | T | G | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0182 others(5): Show |
8 | HG00642.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+2249T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879611 | |||||||
chr2:237879622 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
90 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.191+2260A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879622 | |||||||
chr2:237879690 | T | TA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
215 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.191+2342dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879690 | ||||||
chr2:237879705 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
116 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.191+2343T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879705 | |||||||
chr2:237879771 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0394 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.191+2409A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879771 | |||||||
chr2:237879846 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0222 a0001c0001t0003g0223 |
3 | HG02717.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.191+2484C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879846 | |||||||
chr2:237879847 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0001g0235 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+2485G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879847 | |||||||
chr2:237879883 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
90 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.191+2521G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879883 | |||||||
chr2:237879934 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.191+2572G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879934 | |||||||
chr2:237879947 | G | A | 2 | a0001c0001t0003g0126 a0001c0001t0004g0127 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+2585G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237879947 | |||||||
chr2:237879989 | C | CA | 31 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0057 others(28): Show |
31 | HG00544.hp1 HG00597.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+2649dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | C | CAA | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(38): Show |
43 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.191+2648_191+2649d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | C | CAAA | 70 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
71 | HG01074.hp1 HG01099.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.191+2647_191+2649d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | C | CAAAA | 18 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
18 | HG00408.hp1 HG00642.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.191+2646_191+2649d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | C | CAAAAA | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(44): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.191+2645_191+2649d others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | C | CAAAAAA | 12 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0143 others(9): Show |
12 | HG00621.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+2644_191+2649d others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237879989 | CA | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0001t0001g0096 others(9): Show |
12 | HG01261.hp2 HG02132.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.191+2649delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237879989 | ||||||
chr2:237880026 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0121 others(17): Show |
20 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.191+2664G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880026 | |||||||
chr2:237880079 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0222 a0001c0001t0003g0223 |
3 | HG02717.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.191+2717G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880079 | |||||||
chr2:237880156 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+2794G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880156 | |||||||
chr2:237880185 | CACAG | C | 19 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0133 others(16): Show |
19 | HG01099.hp1 HG01175.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.191+2829_191+2832d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237880185 | ||||||
chr2:237880188 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.191+2826A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880188 | |||||||
chr2:237880215 | G | A | 19 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(16): Show |
19 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.191+2853G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880215 | |||||||
chr2:237880232 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+2870T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880232 | |||||||
chr2:237880250 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(64): Show |
71 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.191+2888C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880250 | |||||||
chr2:237880275 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(206): Show |
216 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.191+2913G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880275 | |||||||
chr2:237880379 | C | T | 28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
28 | HG00609.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.191+3017C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880379 | |||||||
chr2:237880398 | C | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+3036C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880398 | |||||||
chr2:237880402 | G | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
354 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.191+3040G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880402 | |||||||
chr2:237880552 | A | G | 15 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+3190A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880552 | |||||||
chr2:237880553 | C | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
87 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.191+3191C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880553 | |||||||
chr2:237880961 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0164 a0001c0002t0001g0329 others(1): Show |
4 | HG02258.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+3599G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880961 | |||||||
chr2:237880970 | C | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(16): Show |
21 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.191+3608C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880970 | |||||||
chr2:237880993 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
83 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.191+3631C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237880993 | |||||||
chr2:237881133 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.191+3771C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881133 | |||||||
chr2:237881216 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(114): Show |
121 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.191+3854C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881216 | |||||||
chr2:237881250 | T | C | 15 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0146 others(12): Show |
15 | HG00544.hp1 HG02056.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.191+3888T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881250 | |||||||
chr2:237881280 | G | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.191+3918G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881280 | |||||||
chr2:237881454 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.191+4092G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881454 | |||||||
chr2:237881500 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0159 others(5): Show |
8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+4138G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881500 | |||||||
chr2:237881544 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0003g0126 a0001c0001t0004g0127 |
3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4182G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881544 | |||||||
chr2:237881547 | T | C | 9 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0159 others(6): Show |
9 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+4185T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881547 | |||||||
chr2:237881603 | G | C | 3 | a0001c0001t0001g0210 a0001c0001t0003g0126 a0001c0001t0004g0127 |
3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4241G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237881603 | |||||||
chr2:237881993 | TCCTCTAG | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+4635_191+4641d others(9): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237881993 | ||||||
chr2:237882004 | G | T | 3 | a0001c0001t0001g0210 a0001c0001t0003g0126 a0001c0001t0004g0127 |
3 | HG00642.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.191+4642G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882004 | |||||||
chr2:237882132 | ATGCAAAC others(9): Show |
A | 1 | a0001c0001t0001g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.191+4774_191+4789d others(18): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882132 | ||||||
chr2:237882142 | C | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(139): Show |
146 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.191+4780C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882142 | |||||||
chr2:237882156 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+4794C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882156 | |||||||
chr2:237882188 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.191+4826A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882188 | |||||||
chr2:237882255 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.191+4893C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882255 | |||||||
chr2:237882368 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+5006C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882368 | |||||||
chr2:237882424 | G | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
85 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.191+5062G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882424 | |||||||
chr2:237882487 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
63 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.191+5125G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882487 | |||||||
chr2:237882524 | C | A | 15 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0161 others(12): Show |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+5162C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882524 | |||||||
chr2:237882524 | C | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
63 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.191+5162C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882524 | |||||||
chr2:237882702 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.191+5340C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882702 | |||||||
chr2:237882741 | T | C | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5379T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882741 | |||||||
chr2:237882754 | G | A | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(348): Show |
360 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.191+5392G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882754 | |||||||
chr2:237882820 | A | AGGCCATC others(10): Show |
67 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
70 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.191+5462_191+5478d others(19): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882820 | ||||||
chr2:237882820 | A | AGGCCATC others(27): Show |
1 | a0001c0001t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.191+5478_191+5479i others(36): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237882820 | ||||||
chr2:237882844 | T | C | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5482T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882844 | |||||||
chr2:237882867 | C | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5505C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882867 | |||||||
chr2:237882913 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
174 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.191+5551T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882913 | |||||||
chr2:237882914 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+5552G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882914 | |||||||
chr2:237882971 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0159 others(5): Show |
8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+5609G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237882971 | |||||||
chr2:237883015 | A | G | 1 | a0001c0002t0001g0343 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.191+5653A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883015 | |||||||
chr2:237883021 | G | C | 8 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0159 others(5): Show |
8 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+5659G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883021 | |||||||
chr2:237883184 | G | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+5822G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883184 | |||||||
chr2:237883279 | G | A | 42 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
42 | HG00544.hp1 HG00741.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.191+5917G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883279 | |||||||
chr2:237883310 | G | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG01496.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+5948G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883310 | |||||||
chr2:237883341 | AG | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0045 others(52): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.191+5981delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883341 | ||||||
chr2:237883361 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
217 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.191+5999A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883361 | |||||||
chr2:237883491 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
222 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.191+6129A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883491 | |||||||
chr2:237883496 | G | A | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+6134G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883496 | |||||||
chr2:237883558 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0003g0223 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.191+6196G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883558 | |||||||
chr2:237883564 | C | T | 1 | a0001c0002t0001g0333 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.191+6202C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883564 | |||||||
chr2:237883749 | A | G | 2 | a0001c0001t0001g0296 a0001c0002t0001g0351 |
2 | HG03490.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.191+6387A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883749 | |||||||
chr2:237883776 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.191+6414A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237883776 | |||||||
chr2:237883816 | C | CA | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(46): Show |
53 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.191+6468dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883816 | ||||||
chr2:237883816 | CA | C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+6468delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883816 | ||||||
chr2:237883818 | AAAAAAAA others(16): Show |
A | 1 | a0001c0002t0001g0350 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.191+6471_191+6493d others(25): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883818 | ||||||
chr2:237883827 | AAAAG | A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0130 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+6469_191+6472d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883827 | ||||||
chr2:237883912 | C | CT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(95): Show |
100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.191+6574dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | ||||||
chr2:237883912 | C | CTT | 48 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
51 | HG00323.hp2 HG00558.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.191+6573_191+6574d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | ||||||
chr2:237883912 | C | CTTT | 22 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0137 others(19): Show |
22 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+6572_191+6574d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | ||||||
chr2:237883912 | CT | C | 16 | a0001c0001t0001g0164 a0001c0001t0001g0183 a0001c0001t0001g0192 others(13): Show |
16 | HG01074.hp1 HG02071.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+6574delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237883912 | ||||||
chr2:237884301 | T | G | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG00735.hp1 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+6939T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884301 | |||||||
chr2:237884308 | A | G | 1 | a0001c0002t0001g0389 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.191+6946A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884308 | |||||||
chr2:237884383 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(11): Show |
15 | HG00642.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+7021C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884383 | |||||||
chr2:237884426 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(128): Show |
132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.191+7064G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884426 | |||||||
chr2:237884622 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.191+7260G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884622 | |||||||
chr2:237884624 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.191+7262G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884624 | |||||||
chr2:237884826 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.191+7464C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884826 | |||||||
chr2:237884888 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191+7526G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884888 | |||||||
chr2:237884889 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191+7527A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884889 | |||||||
chr2:237884903 | C | T | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+7541C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884903 | |||||||
chr2:237884932 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+7570G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884932 | |||||||
chr2:237884942 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+7580G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237884942 | |||||||
chr2:237885023 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+7661C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885023 | |||||||
chr2:237885120 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.191+7758T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885120 | |||||||
chr2:237885130 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191+7768G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885130 | |||||||
chr2:237885210 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.191+7848G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885210 | |||||||
chr2:237885231 | CGAG | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0096 others(45): Show |
49 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+7871_191+7873d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237885231 | ||||||
chr2:237885236 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
58 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.191+7874G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885236 | |||||||
chr2:237885434 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+8072G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885434 | |||||||
chr2:237885439 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0181 |
2 | HG01255.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.191+8077C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885439 | |||||||
chr2:237885487 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.191+8125A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885487 | |||||||
chr2:237885539 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.191+8177C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885539 | |||||||
chr2:237885572 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.191+8210C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885572 | |||||||
chr2:237885589 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0205 a0001c0001t0001g0208 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+8227G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885589 | |||||||
chr2:237885604 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(50): Show |
57 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.191+8242G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885604 | |||||||
chr2:237885667 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.191+8305G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885667 | |||||||
chr2:237885810 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0292 |
2 | HG00673.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.191+8448C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885810 | |||||||
chr2:237885812 | T | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0323 |
3 | HG03209.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.191+8450T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885812 | |||||||
chr2:237885860 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0118 |
3 | HG01891.hp2 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.191+8498C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237885860 | |||||||
chr2:237886062 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
267 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.191+8700A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886062 | |||||||
chr2:237886092 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0087 others(7): Show |
10 | HG01496.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+8730T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886092 | |||||||
chr2:237886100 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0087 others(5): Show |
8 | HG02486.hp2 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.191+8738G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886100 | |||||||
chr2:237886218 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(6): Show |
9 | HG00609.hp1 HG01123.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.191+8856G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886218 | |||||||
chr2:237886310 | A | G | 1 | a0001c0002t0001g0345 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.191+8948A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886310 | |||||||
chr2:237886321 | C | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
35 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.191+8959C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886321 | |||||||
chr2:237886342 | C | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG01496.hp1 HG02071.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+8980C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886342 | |||||||
chr2:237886369 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(264): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.191+9007G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886369 | |||||||
chr2:237886384 | C | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0146 a0001c0001t0001g0222 others(3): Show |
6 | HG02071.hp2 HG03098.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+9022C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886384 | |||||||
chr2:237886451 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0142 |
3 | HG02886.hp1 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191+9089G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886451 | |||||||
chr2:237886569 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.191+9207G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886569 | |||||||
chr2:237886616 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0205 a0001c0001t0003g0223 |
3 | HG02717.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.191+9254G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886616 | |||||||
chr2:237886652 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.191+9290C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886652 | |||||||
chr2:237886656 | G | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0014 others(26): Show |
30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.191+9294G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886656 | |||||||
chr2:237886708 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.191+9346C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886708 | |||||||
chr2:237886735 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.191+9373C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886735 | |||||||
chr2:237886807 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+9445C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886807 | |||||||
chr2:237886814 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0002g0316 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191+9452G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886814 | |||||||
chr2:237886831 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
36 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.191+9469C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886831 | |||||||
chr2:237886839 | C | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.191+9477C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886839 | |||||||
chr2:237886876 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0002g0186 |
3 | HG02109.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191+9514G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886876 | |||||||
chr2:237886911 | T | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.191+9549T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886911 | |||||||
chr2:237886945 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.191+9583G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886945 | |||||||
chr2:237886960 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(172): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.191+9598A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886960 | |||||||
chr2:237886991 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0064 |
3 | HG03490.hp1 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.191+9629G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886991 | |||||||
chr2:237886998 | C | T | 1 | a0001c0002t0001g0382 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.191+9636C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237886998 | |||||||
chr2:237887000 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.191+9638G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887000 | |||||||
chr2:237887010 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0201 a0001c0001t0001g0314 others(1): Show |
4 | HG00735.hp1 HG01978.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+9648G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887010 | |||||||
chr2:237887091 | G | T | 1 | a0001c0001t0001g0291 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+9729G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887091 | |||||||
chr2:237887144 | C | T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0119 others(45): Show |
49 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+9782C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887144 | |||||||
chr2:237887177 | G | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG00735.hp1 HG01358.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+9815G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887177 | |||||||
chr2:237887411 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+10049T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887411 | |||||||
chr2:237887413 | A | AGTATCAA others(3): Show |
46 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0119 others(43): Show |
47 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.191+10052_191+1005 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237887413 | ||||||
chr2:237887436 | C | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG00733.hp2 HG03927.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.191+10074C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887436 | |||||||
chr2:237887478 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.191+10116G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887478 | |||||||
chr2:237887737 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.191+10375G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887737 | |||||||
chr2:237887845 | C | T | 1 | a0001c0001t0001g0006 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.191+10483C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887845 | |||||||
chr2:237887898 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.191+10536A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887898 | |||||||
chr2:237887908 | T | C | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+10546T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887908 | |||||||
chr2:237887962 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(134): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.191+10600T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237887962 | |||||||
chr2:237888011 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(167): Show |
175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.191+10649G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888011 | |||||||
chr2:237888012 | CA | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10652delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237888012 | ||||||
chr2:237888056 | T | A | 1 | a0001c0001t0001g0291 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.191+10694T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888056 | |||||||
chr2:237888056 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.191+10694T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888056 | |||||||
chr2:237888057 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(131): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.191+10695G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888057 | |||||||
chr2:237888062 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0155 |
2 | HG02056.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.191+10700G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888062 | |||||||
chr2:237888093 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10731G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888093 | |||||||
chr2:237888106 | T | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
34 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.191+10744T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888106 | |||||||
chr2:237888193 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0003g0232 |
2 | HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.191+10831A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888193 | |||||||
chr2:237888243 | CAG | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0002g0186 |
3 | HG02109.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191+10882_191+1088 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888243 | |||||||
chr2:237888260 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0212 others(1): Show |
4 | HG01081.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+10898G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888260 | |||||||
chr2:237888457 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11095G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888457 | |||||||
chr2:237888495 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+11136dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237888495 | ||||||
chr2:237888581 | G | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11219G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888581 | |||||||
chr2:237888716 | A | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0119 others(45): Show |
49 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.191+11354A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888716 | |||||||
chr2:237888794 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
39 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.191+11432C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888794 | |||||||
chr2:237888804 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+11442C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888804 | |||||||
chr2:237888817 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
37 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.191+11455G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888817 | |||||||
chr2:237888818 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
37 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.191+11456C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888818 | |||||||
chr2:237888891 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.191+11529C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888891 | |||||||
chr2:237888928 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.191+11566C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237888928 | |||||||
chr2:237889061 | G | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0087 others(19): Show |
22 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.191+11699G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889061 | |||||||
chr2:237889110 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0001g0235 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+11748C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889110 | |||||||
chr2:237889146 | T | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.191+11784T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889146 | |||||||
chr2:237889167 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
74 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.191+11805T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889167 | |||||||
chr2:237889190 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0145 a0001c0001t0003g0021 |
3 | HG02818.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.191+11828A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889190 | |||||||
chr2:237889227 | G | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0119 others(43): Show |
47 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.191+11865G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889227 | |||||||
chr2:237889518 | C | G | 1 | a0001c0001t0001g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.191+12156C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889518 | |||||||
chr2:237889532 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0323 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.191+12170C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889532 | |||||||
chr2:237889938 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.191+12576G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889938 | |||||||
chr2:237889998 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0320 others(1): Show |
4 | HG02486.hp2 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+12636G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237889998 | |||||||
chr2:237890016 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.191+12654G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890016 | |||||||
chr2:237890022 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191+12660G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890022 | |||||||
chr2:237890026 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191+12664C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890026 | |||||||
chr2:237890035 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191+12673C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890035 | |||||||
chr2:237890106 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0145 others(9): Show |
12 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+12744C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890106 | |||||||
chr2:237890207 | T | A | 16 | a0001c0001t0001g0087 a0001c0001t0001g0140 a0001c0001t0001g0144 others(13): Show |
16 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.191+12845T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890207 | |||||||
chr2:237890263 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0002g0316 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191+12901G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890263 | |||||||
chr2:237890275 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.191+12913C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890275 | |||||||
chr2:237890287 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(114): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.191+12925C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890287 | |||||||
chr2:237890360 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.191+12998C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890360 | |||||||
chr2:237890454 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(36): Show |
42 | HG00438.hp2 HG01070.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.191+13092G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890454 | |||||||
chr2:237890494 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0145 a0001c0001t0001g0170 others(1): Show |
4 | HG02818.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+13132A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890494 | |||||||
chr2:237890497 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+13135G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890497 | |||||||
chr2:237890564 | C | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.191+13202C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890564 | |||||||
chr2:237890685 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0246 a0001c0001t0001g0247 others(4): Show |
7 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13323T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890685 | |||||||
chr2:237890729 | TCCTTTAC others(12): Show |
T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+13372_191+1339 others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237890729 | ||||||
chr2:237890736 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.191+13374C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890736 | |||||||
chr2:237890853 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+13491G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890853 | |||||||
chr2:237890872 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(125): Show |
131 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.191+13510G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890872 | |||||||
chr2:237890907 | C | A | 1 | a0001c0002t0001g0369 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.191+13545C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890907 | |||||||
chr2:237890923 | C | T | 32 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0087 others(29): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.191+13561C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237890923 | |||||||
chr2:237891145 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+13783T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891145 | |||||||
chr2:237891150 | TTC | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0093 others(3): Show |
7 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13792_191+1379 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891150 | ||||||
chr2:237891154 | C | CT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0102 others(6): Show |
9 | HG02559.hp1 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.191+13805dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891154 | ||||||
chr2:237891154 | CT | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0109 a0001c0001t0001g0129 others(4): Show |
7 | HG01496.hp1 HG02148.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+13805delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237891154 | ||||||
chr2:237891195 | A | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.191+13833A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891195 | |||||||
chr2:237891196 | G | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.191+13834G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891196 | |||||||
chr2:237891198 | GA | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.191+13837delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891198 | |||||||
chr2:237891201 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.191+13839G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891201 | |||||||
chr2:237891215 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
261 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.191+13853G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891215 | |||||||
chr2:237891244 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0093 others(3): Show |
7 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+13882G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891244 | |||||||
chr2:237891385 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.191+14023C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891385 | |||||||
chr2:237891442 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.191+14080G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891442 | |||||||
chr2:237891578 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0391 |
2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.191+14216G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891578 | |||||||
chr2:237891740 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.191+14378G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891740 | |||||||
chr2:237891829 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.191+14467T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891829 | |||||||
chr2:237891957 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.191+14595C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237891957 | |||||||
chr2:237892181 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191+14819C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892181 | |||||||
chr2:237892232 | T | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(81): Show |
86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.191+14870T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892232 | |||||||
chr2:237892276 | CT | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0037 others(71): Show |
75 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.191+14934delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892276 | ||||||
chr2:237892279 | T | TC | 7 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0163 others(4): Show |
7 | HG01106.hp1 HG01346.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+14917_191+1491 others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892279 | |||||||
chr2:237892280 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.191+14918T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892280 | |||||||
chr2:237892281 | T | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0100 others(5): Show |
8 | HG01496.hp1 HG01515.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+14919T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892281 | |||||||
chr2:237892320 | G | A | 20 | a0001c0001t0001g0087 a0001c0001t0001g0140 a0001c0001t0001g0144 others(17): Show |
20 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.191+14958G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892320 | |||||||
chr2:237892457 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.191+15095A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892457 | |||||||
chr2:237892655 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(248): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.191+15293C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237892655 | |||||||
chr2:237892735 | T | TTC | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.191+15395_191+1539 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237892735 | T | TTCTC | 30 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0039 others(27): Show |
31 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.191+15393_191+1539 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237892735 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.191+15387_191+1539 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237892735 | TTC | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0089 a0001c0002t0001g0350 |
3 | HG01261.hp2 HG03239.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.191+15395_191+1539 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237892735 | TTCTC | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0042 others(44): Show |
48 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.191+15393_191+1539 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237892735 | TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0002g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191+15387_191+1539 others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237892735 | ||||||
chr2:237893144 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(84): Show |
90 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.191+15782A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893144 | |||||||
chr2:237893240 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.191+15878A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893240 | |||||||
chr2:237893657 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0240 a0001c0002t0001g0336 others(1): Show |
4 | HG01074.hp2 HG02071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+16295G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893657 | |||||||
chr2:237893770 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0093 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+16408C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893770 | |||||||
chr2:237893809 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0395 |
3 | HG02109.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.191+16447C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893809 | |||||||
chr2:237893969 | TC | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0119 a0001c0001t0001g0130 others(20): Show |
24 | HG01255.hp1 HG01346.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.191+16608delC | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893969 | |||||||
chr2:237893970 | C | CT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0055 others(13): Show |
16 | HG01167.hp1 HG01496.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.191+16627dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | ||||||
chr2:237893970 | C | CTT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(41): Show |
45 | HG00099.hp2 HG01169.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.191+16626_191+1662 others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | ||||||
chr2:237893970 | C | CTTT | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.191+16625_191+1662 others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | ||||||
chr2:237893970 | C | CTTTT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(12): Show |
15 | HG01175.hp2 HG01891.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.191+16624_191+1662 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237893970 | ||||||
chr2:237893970 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02647.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.191+16608C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237893970 | |||||||
chr2:237894197 | C | T | 1 | a0001c0001t0001g0395 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.191+16835C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894197 | |||||||
chr2:237894268 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.191+16906G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894268 | |||||||
chr2:237894288 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0093 others(4): Show |
7 | HG02486.hp2 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.191+16926A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894288 | |||||||
chr2:237894470 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192-17058G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894470 | |||||||
chr2:237894476 | G | A | 1 | a0001c0002t0001g0343 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.192-17052G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894476 | |||||||
chr2:237894551 | C | T | 11 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0001t0001g0131 others(8): Show |
11 | HG00642.hp2 HG01099.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-16977C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894551 | |||||||
chr2:237894652 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-16876A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894652 | |||||||
chr2:237894654 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.192-16874G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894654 | |||||||
chr2:237894744 | C | G | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(334): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.192-16784C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894744 | |||||||
chr2:237894773 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.192-16755C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894773 | |||||||
chr2:237894776 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0205 a0001c0001t0001g0222 others(2): Show |
5 | HG02717.hp1 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-16752C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894776 | |||||||
chr2:237894836 | A | G | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(340): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.192-16692A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894836 | |||||||
chr2:237894900 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-16628G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894900 | |||||||
chr2:237894932 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0122 |
3 | HG02145.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.192-16596C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894932 | |||||||
chr2:237894938 | G | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(1): Show |
4 | NA18961.hp2 NA18962.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-16590G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237894938 | |||||||
chr2:237895280 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.192-16248G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895280 | |||||||
chr2:237895284 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0307 |
2 | NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.192-16244G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895284 | |||||||
chr2:237895346 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0308 |
2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.192-16182C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895346 | |||||||
chr2:237895427 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(105): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.192-16101A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895427 | |||||||
chr2:237895453 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192-16075G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895453 | |||||||
chr2:237895520 | T | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
352 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.192-16008T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895520 | |||||||
chr2:237895547 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(105): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.192-15981G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895547 | |||||||
chr2:237895583 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.192-15945C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895583 | |||||||
chr2:237895645 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.192-15883C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895645 | |||||||
chr2:237895655 | G | A | 1 | a0001c0002t0001g0348 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192-15873G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895655 | |||||||
chr2:237895703 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(104): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.192-15825A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895703 | |||||||
chr2:237895713 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.192-15815T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895713 | |||||||
chr2:237895729 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.192-15799C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895729 | |||||||
chr2:237895775 | G | A | 1 | a0001c0001t0001g0003 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.192-15753G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895775 | |||||||
chr2:237895803 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(91): Show |
95 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.192-15725C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895803 | |||||||
chr2:237895843 | T | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(103): Show |
108 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.192-15685T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895843 | |||||||
chr2:237895901 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192-15627G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237895901 | |||||||
chr2:237896098 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.192-15430G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896098 | |||||||
chr2:237896256 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-15272C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896256 | |||||||
chr2:237896264 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(106): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.192-15264T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896264 | |||||||
chr2:237896372 | T | C | 2 | a0001c0001t0001g0392 a0001c0001t0001g0393 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.192-15156T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896372 | |||||||
chr2:237896373 | C | G | 3 | a0001c0001t0001g0205 a0001c0001t0002g0186 a0001c0001t0003g0223 |
3 | HG02717.hp1 HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.192-15155C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896373 | |||||||
chr2:237896477 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.192-15051C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896477 | |||||||
chr2:237896535 | C | T | 1 | a0001c0002t0001g0367 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.192-14993C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896535 | |||||||
chr2:237896685 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192-14843G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896685 | |||||||
chr2:237896832 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.192-14696G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237896832 | |||||||
chr2:237897028 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192-14500G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897028 | |||||||
chr2:237897123 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0170 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.192-14405G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897123 | |||||||
chr2:237897421 | T | C | 1 | a0001c0001t0004g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.192-14107T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897421 | |||||||
chr2:237897432 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192-14096T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897432 | |||||||
chr2:237897442 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.192-14086C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897442 | |||||||
chr2:237897541 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.192-13987C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897541 | |||||||
chr2:237897728 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.192-13800T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897728 | |||||||
chr2:237897771 | G | GT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0164 others(6): Show |
10 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.192-13751dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897771 | ||||||
chr2:237897771 | GT | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0221 a0001c0001t0001g0241 others(4): Show |
7 | HG01168.hp1 HG02071.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-13751delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897771 | ||||||
chr2:237897777 | T | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.192-13751T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897777 | |||||||
chr2:237897777 | T | TG | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.192-13742dupG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897777 | ||||||
chr2:237897777 | TG | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(99): Show |
104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.192-13742delG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897777 | ||||||
chr2:237897787 | T | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0058 others(33): Show |
38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.192-13741T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897787 | |||||||
chr2:237897794 | T | TTTTG | 6 | a0001c0001t0001g0108 a0001c0001t0001g0241 a0001c0001t0002g0234 others(3): Show |
6 | HG01168.hp1 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-13718_192-1371 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237897794 | ||||||
chr2:237897910 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0003g0223 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-13618T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897910 | |||||||
chr2:237897915 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.192-13613C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897915 | |||||||
chr2:237897955 | C | T | 1 | a0001c0001t0001g0391 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.192-13573C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897955 | |||||||
chr2:237897965 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.192-13563A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237897965 | |||||||
chr2:237898332 | G | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0164 a0001c0001t0002g0186 others(4): Show |
7 | HG02258.hp1 HG02723.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-13196G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898332 | |||||||
chr2:237898415 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.192-13113G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898415 | |||||||
chr2:237898435 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.192-13093G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898435 | |||||||
chr2:237898527 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0142 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-13001G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898527 | |||||||
chr2:237898542 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.192-12986A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898542 | |||||||
chr2:237898682 | C | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0256 others(1): Show |
4 | HG01928.hp1 NA18943.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-12846C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898682 | |||||||
chr2:237898738 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0170 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.192-12790G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898738 | |||||||
chr2:237898743 | C | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0048 others(4): Show |
7 | HG00558.hp2 NA18951.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-12785C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898743 | |||||||
chr2:237898807 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.192-12721C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898807 | |||||||
chr2:237898808 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.192-12720A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898808 | |||||||
chr2:237898819 | G | A | 1 | a0001c0002t0001g0370 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.192-12709G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898819 | |||||||
chr2:237898872 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.192-12656G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237898872 | |||||||
chr2:237899013 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0001g0218 a0001c0001t0001g0219 others(6): Show |
9 | HG01168.hp1 HG02071.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.192-12515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899013 | |||||||
chr2:237899072 | A | AT | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.192-12444dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237899072 | ||||||
chr2:237899140 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.192-12388C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899140 | |||||||
chr2:237899310 | A | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0054 |
2 | HG02523.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.192-12218A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899310 | |||||||
chr2:237899496 | C | T | 9 | a0001c0001t0001g0093 a0001c0001t0001g0164 a0001c0001t0001g0205 others(6): Show |
9 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.192-12032C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899496 | |||||||
chr2:237899662 | G | T | 2 | a0001c0001t0001g0205 a0001c0001t0003g0223 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-11866G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899662 | |||||||
chr2:237899725 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.192-11803G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899725 | |||||||
chr2:237899838 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.192-11690A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899838 | |||||||
chr2:237899931 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0002g0186 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-11597G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899931 | |||||||
chr2:237899955 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.192-11573C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237899955 | |||||||
chr2:237900124 | ACTT | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0125 a0001c0001t0001g0139 |
4 | HG02055.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-11397_192-1139 others(7): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237900124 | ||||||
chr2:237900282 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0003g0223 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.192-11246C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900282 | |||||||
chr2:237900466 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192-11062T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900466 | |||||||
chr2:237900466 | T | TA | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.192-11062_192-1106 others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900466 | |||||||
chr2:237900556 | TTTTG | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0145 a0001c0001t0003g0021 |
3 | HG02818.hp1 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.192-10968_192-1096 others(8): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237900556 | ||||||
chr2:237900595 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.192-10933T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900595 | |||||||
chr2:237900763 | A | T | 22 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(19): Show |
22 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.192-10765A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900763 | |||||||
chr2:237900804 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0002g0186 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-10724T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237900804 | |||||||
chr2:237901062 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192-10466G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901062 | |||||||
chr2:237901081 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.192-10447C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901081 | |||||||
chr2:237901083 | G | A | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(339): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.192-10445G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901083 | |||||||
chr2:237901145 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0002g0186 |
2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192-10383G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901145 | |||||||
chr2:237901208 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-10320C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901208 | |||||||
chr2:237901273 | G | T | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(339): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.192-10255G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901273 | |||||||
chr2:237901374 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0129 others(2): Show |
5 | HG01496.hp1 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-10154A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901374 | |||||||
chr2:237901430 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0076 |
3 | HG01069.hp2 HG01071.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.192-10098T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901430 | |||||||
chr2:237901660 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.192-9868G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901660 | |||||||
chr2:237901699 | C | T | 14 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0131 others(11): Show |
14 | HG01074.hp1 HG01099.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.192-9829C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901699 | |||||||
chr2:237901837 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.192-9691T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901837 | |||||||
chr2:237901860 | T | TACTC | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.192-9664_192-9661d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237901860 | ||||||
chr2:237901934 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.192-9594C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237901934 | |||||||
chr2:237902086 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.192-9442G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902086 | |||||||
chr2:237902102 | T | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0037 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-9426T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902102 | |||||||
chr2:237902121 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.192-9407G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902121 | |||||||
chr2:237902177 | C | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0055 others(14): Show |
18 | HG01099.hp2 HG01123.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.192-9351C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902177 | |||||||
chr2:237902298 | A | AGGAGGAG others(32): Show |
1 | a0001c0001t0001g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.192-9202_192-9164d others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | ||||||
chr2:237902298 | A | AGGAGGAG others(71): Show |
1 | a0001c0004t0005g0178 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.192-9164_192-9163i others(80): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | ||||||
chr2:237902298 | AGGAGGAG others(32): Show |
A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.192-9202_192-9164d others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902298 | ||||||
chr2:237902300 | G | GAGGAGGG others(13): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0125 a0001c0001t0001g0139 others(1): Show |
5 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-9211_192-9210i others(22): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902300 | ||||||
chr2:237902337 | T | TGGAGGAG others(32): Show |
1 | a0001c0001t0001g0297 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.192-9164_192-9163i others(41): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237902337 | ||||||
chr2:237902450 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
42 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.192-9078C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902450 | |||||||
chr2:237902452 | C | T | 2 | a0001c0001t0001g0255 a0001c0002t0001g0370 |
2 | HG02129.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.192-9076C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902452 | |||||||
chr2:237902463 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0089 a0001c0001t0001g0180 others(2): Show |
5 | HG00735.hp1 HG01261.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-9065G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902463 | |||||||
chr2:237902474 | G | C | 1 | a0001c0002t0001g0345 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.192-9054G>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902474 | |||||||
chr2:237902581 | G | A | 1 | a0001c0002t0001g0340 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.192-8947G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902581 | |||||||
chr2:237902591 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
39 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.192-8937G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902591 | |||||||
chr2:237902651 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0125 others(6): Show |
10 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-8877T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902651 | |||||||
chr2:237902659 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0122 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-8869A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902659 | |||||||
chr2:237902670 | A | G | 154 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(151): Show |
156 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.192-8858A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902670 | |||||||
chr2:237902748 | A | T | 1 | a0001c0002t0001g0381 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192-8780A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902748 | |||||||
chr2:237902873 | A | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0058 others(21): Show |
24 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.192-8655A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902873 | |||||||
chr2:237902974 | C | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0123 others(4): Show |
7 | HG01358.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-8554C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237902974 | |||||||
chr2:237903089 | C | G | 68 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0019 others(65): Show |
68 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.192-8439C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903089 | |||||||
chr2:237903123 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192-8405T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903123 | |||||||
chr2:237903180 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0195 |
3 | HG01255.hp1 HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.192-8348T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903180 | |||||||
chr2:237903187 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0067 others(9): Show |
12 | HG01515.hp2 HG02071.hp2 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.192-8341A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903187 | |||||||
chr2:237903260 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0037 others(12): Show |
16 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.192-8268C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903260 | |||||||
chr2:237903261 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192-8267G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903261 | |||||||
chr2:237903394 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.192-8134C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903394 | |||||||
chr2:237903474 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00597.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.192-8054T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903474 | |||||||
chr2:237903480 | T | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-8048T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903480 | |||||||
chr2:237903501 | C | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-8027C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903501 | |||||||
chr2:237903522 | A | C | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(358): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.192-8006A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903522 | |||||||
chr2:237903527 | CT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(18): Show |
22 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.192-7992delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237903527 | ||||||
chr2:237903551 | T | C | 349 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(346): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.192-7977T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903551 | |||||||
chr2:237903604 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.192-7924A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903604 | |||||||
chr2:237903680 | G | T | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(356): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.192-7848G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903680 | |||||||
chr2:237903765 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0209 |
2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.192-7763G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903765 | |||||||
chr2:237903787 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.192-7741C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903787 | |||||||
chr2:237903844 | G | A | 1 | a0001c0002t0001g0381 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192-7684G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903844 | |||||||
chr2:237903851 | C | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(221): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.192-7677C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903851 | |||||||
chr2:237903855 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-7673C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903855 | |||||||
chr2:237903918 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192-7610T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237903918 | |||||||
chr2:237904004 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0326 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.192-7524G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904004 | |||||||
chr2:237904010 | T | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(27): Show |
32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.192-7518T>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904010 | |||||||
chr2:237904031 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0184 |
2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.192-7497G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904031 | |||||||
chr2:237904165 | G | A | 8 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0157 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-7363G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904165 | |||||||
chr2:237904177 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.192-7351T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904177 | |||||||
chr2:237904195 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-7333C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904195 | |||||||
chr2:237904196 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-7332G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904196 | |||||||
chr2:237904257 | C | CA | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.192-7259dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237904257 | ||||||
chr2:237904257 | CA | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(28): Show |
32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.192-7259delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237904257 | ||||||
chr2:237904279 | C | T | 50 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0025 others(47): Show |
51 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.192-7249C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904279 | |||||||
chr2:237904287 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.192-7241C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904287 | |||||||
chr2:237904469 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | NA18961.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.192-7059G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904469 | |||||||
chr2:237904632 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192-6896C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904632 | |||||||
chr2:237904642 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0077 others(5): Show |
8 | HG00735.hp1 HG01255.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.192-6886G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904642 | |||||||
chr2:237904807 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192-6721C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904807 | |||||||
chr2:237904913 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.192-6615C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904913 | |||||||
chr2:237904941 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.192-6587C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237904941 | |||||||
chr2:237905025 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0129 |
2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-6503C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905025 | |||||||
chr2:237905032 | T | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(67): Show |
71 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.192-6496T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905032 | |||||||
chr2:237905305 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.192-6223A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905305 | |||||||
chr2:237905681 | G | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG02280.hp1 HG03195.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-5847G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905681 | |||||||
chr2:237905714 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.192-5814A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905714 | |||||||
chr2:237905748 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.192-5780C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905748 | |||||||
chr2:237905858 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0152 |
2 | NA18978.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.192-5670A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905858 | |||||||
chr2:237905860 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192-5668A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905860 | |||||||
chr2:237905909 | G | A | 16 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0058 others(13): Show |
16 | HG00741.hp2 HG01070.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.192-5619G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905909 | |||||||
chr2:237905967 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192-5561T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237905967 | |||||||
chr2:237906010 | C | CA | 20 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0078 others(17): Show |
20 | HG00438.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.192-5498dupA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | ||||||
chr2:237906010 | C | CAA | 52 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0044 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.192-5499_192-5498d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | ||||||
chr2:237906010 | C | CAAA | 6 | a0001c0001t0001g0110 a0001c0001t0001g0140 a0001c0001t0001g0163 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-5500_192-5498d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | ||||||
chr2:237906010 | CA | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(118): Show |
123 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.192-5498delA | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906010 | ||||||
chr2:237906037 | A | G | 369 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(366): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.192-5491A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906037 | |||||||
chr2:237906097 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0391 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.192-5431C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906097 | |||||||
chr2:237906181 | A | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.192-5347A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906181 | |||||||
chr2:237906299 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192-5229G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906299 | |||||||
chr2:237906354 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(95): Show |
100 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.192-5174A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906354 | |||||||
chr2:237906585 | T | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0001t0001g0204 others(4): Show |
7 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.192-4943T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906585 | |||||||
chr2:237906610 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.192-4918C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906610 | |||||||
chr2:237906666 | G | A | 15 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0067 others(12): Show |
15 | HG01515.hp2 HG02071.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.192-4862G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906666 | |||||||
chr2:237906717 | C | CT | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.192-4787dupT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | ||||||
chr2:237906717 | C | CTT | 70 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0031 others(67): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.192-4788_192-4787d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | ||||||
chr2:237906717 | C | CTTT | 6 | a0001c0001t0001g0027 a0001c0001t0001g0106 a0001c0001t0001g0183 others(3): Show |
6 | HG01081.hp2 HG02056.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-4789_192-4787d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | ||||||
chr2:237906717 | CT | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0159 others(3): Show |
6 | HG01167.hp1 NA18522.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-4787delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237906717 | ||||||
chr2:237906823 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.192-4705A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906823 | |||||||
chr2:237906847 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.192-4681C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906847 | |||||||
chr2:237906850 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.192-4678G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906850 | |||||||
chr2:237906867 | C | T | 1 | a0001c0001t0001g0003 | 2 | NA18942.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.192-4661C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906867 | |||||||
chr2:237906942 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0129 a0001c0001t0001g0222 |
3 | HG02559.hp1 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.192-4586C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906942 | |||||||
chr2:237906965 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-4563C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906965 | |||||||
chr2:237906966 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.192-4562G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237906966 | |||||||
chr2:237907059 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.192-4469T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907059 | |||||||
chr2:237907122 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0230 |
2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.192-4406C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907122 | |||||||
chr2:237907236 | T | C | 370 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(367): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.192-4292T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907236 | |||||||
chr2:237907314 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0394 |
2 | HG01074.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.192-4214G>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907314 | |||||||
chr2:237907335 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.192-4193C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907335 | |||||||
chr2:237907458 | A | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0259 a0001c0002t0001g0343 |
3 | NA18947.hp1 NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.192-4070A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907458 | |||||||
chr2:237907490 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192-4038G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907490 | |||||||
chr2:237907553 | C | CAT | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.192-3974_192-3973d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237907553 | ||||||
chr2:237907559 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0025 others(80): Show |
84 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.192-3969C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907559 | |||||||
chr2:237907714 | A | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.192-3814A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907714 | |||||||
chr2:237907729 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.192-3799G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907729 | |||||||
chr2:237907946 | T | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(220): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.192-3582T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237907946 | |||||||
chr2:237908002 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-3526C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908002 | |||||||
chr2:237908039 | A | G | 3 | a0001c0001t0001g0074 a0001c0002t0001g0338 a0001c0002t0001g0385 |
3 | NA18990.hp2 NA19000.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.192-3489A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908039 | |||||||
chr2:237908247 | T | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(24): Show |
28 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.192-3281T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908247 | |||||||
chr2:237908374 | T | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0041 others(14): Show |
17 | HG01515.hp2 HG02071.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.192-3154T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908374 | |||||||
chr2:237908410 | C | CTGG | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0171 others(5): Show |
8 | HG01081.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.192-3091_192-3089d others(5): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(5): Show |
1 | a0001c0001t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.192-3108_192-3107i others(14): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(8): Show |
1 | a0001c0001t0001g0072 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.192-3108_192-3107i others(17): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(11): Show |
1 | a0001c0001t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192-3108_192-3107i others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(11): Show |
211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(208): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.192-3108_192-3107i others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(14): Show |
3 | a0001c0001t0001g0291 a0001c0001t0003g0211 a0001c0002t0001g0386 |
3 | HG02300.hp1 HG03139.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.192-3108_192-3107i others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(11): Show |
1 | a0001c0001t0001g0240 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.192-3106_192-3089d others(20): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908410 | C | CTGGTGGT others(14): Show |
1 | a0001c0001t0001g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.192-3109_192-3089d others(23): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237908410 | ||||||
chr2:237908506 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0139 |
3 | HG02257.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.192-3022C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908506 | |||||||
chr2:237908551 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0145 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.192-2977C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908551 | |||||||
chr2:237908564 | C | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.192-2964C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908564 | |||||||
chr2:237908564 | C | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0068 others(7): Show |
10 | HG00741.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.192-2964C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908564 | |||||||
chr2:237908584 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.192-2944C>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908584 | |||||||
chr2:237908587 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(19): Show |
23 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.192-2941G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908587 | |||||||
chr2:237908657 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.192-2871T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908657 | |||||||
chr2:237908682 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0003g0126 a0001c0001t0003g0211 |
3 | HG03139.hp2 HG03540.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.192-2846C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908682 | |||||||
chr2:237908688 | A | G | 372 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(369): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.192-2840A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908688 | |||||||
chr2:237908715 | T | C | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.192-2813T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908715 | |||||||
chr2:237908872 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0131 others(2): Show |
5 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-2656T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908872 | |||||||
chr2:237908941 | C | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
323 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.192-2587C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237908941 | |||||||
chr2:237909046 | A | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0086 others(21): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.192-2482A>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909046 | |||||||
chr2:237909096 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0087 a0001c0001t0001g0120 others(21): Show |
24 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.192-2432A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909096 | |||||||
chr2:237909118 | C | T | 6 | a0001c0001t0001g0128 a0001c0001t0001g0189 a0001c0001t0001g0196 others(3): Show |
6 | HG01069.hp1 HG01099.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-2410C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909118 | |||||||
chr2:237909132 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.192-2396A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909132 | |||||||
chr2:237909204 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.192-2324G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909204 | |||||||
chr2:237909269 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.192-2259C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909269 | |||||||
chr2:237909300 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.192-2228C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909300 | |||||||
chr2:237909325 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.192-2203C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909325 | |||||||
chr2:237909326 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192-2202G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909326 | |||||||
chr2:237909333 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0261 |
3 | NA18943.hp1 NA18984.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.192-2195A>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909333 | |||||||
chr2:237909343 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.192-2185C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909343 | |||||||
chr2:237909365 | T | TG | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(115): Show |
121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.192-2162dupG | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237909365 | ||||||
chr2:237909375 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
133 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.192-2153G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909375 | |||||||
chr2:237909422 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-2106T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909422 | |||||||
chr2:237909470 | C | T | 5 | a0001c0001t0001g0124 a0001c0001t0001g0144 a0001c0001t0001g0183 others(2): Show |
5 | HG02135.hp1 HG02572.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-2058C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909470 | |||||||
chr2:237909618 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.192-1910G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909618 | |||||||
chr2:237909646 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.192-1882C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909646 | |||||||
chr2:237909655 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.192-1873C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909655 | |||||||
chr2:237909746 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192-1782C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909746 | |||||||
chr2:237909747 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.192-1781A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909747 | |||||||
chr2:237909899 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0326 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.192-1629G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909899 | |||||||
chr2:237909915 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.192-1613G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909915 | |||||||
chr2:237909928 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0027 others(42): Show |
46 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.192-1600C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237909928 | |||||||
chr2:237910009 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.192-1519G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910009 | |||||||
chr2:237910133 | T | C | 387 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(384): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.192-1395T>C | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910133 | |||||||
chr2:237910167 | C | T | 1 | a0001c0002t0001g0365 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.192-1361C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910167 | |||||||
chr2:237910243 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.192-1285C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910243 | |||||||
chr2:237910319 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.192-1209G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910319 | |||||||
chr2:237910383 | TCA | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0027 others(43): Show |
47 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.192-1132_192-1131d others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910383 | ||||||
chr2:237910383 | TCACA | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0087 a0001c0001t0001g0119 others(14): Show |
17 | HG01496.hp1 HG02055.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.192-1134_192-1131d others(6): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910383 | ||||||
chr2:237910426 | TAGAATGT others(9): Show |
T | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.192-1098_192-1083d others(18): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910426 | ||||||
chr2:237910539 | A | ACACACAG others(37): Show |
1 | a0001c0001t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.192-974_192-931dup others(44): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910539 | ||||||
chr2:237910583 | TCACACAG others(21): Show |
T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0198 a0001c0001t0001g0213 |
3 | HG02965.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.192-930_192-903del others(28): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910583 | ||||||
chr2:237910666 | CAG | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0041 others(22): Show |
27 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.192-861_192-860del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910666 | |||||||
chr2:237910678 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192-850G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910678 | |||||||
chr2:237910740 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0004g0127 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.192-788A>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910740 | |||||||
chr2:237910754 | TAGTCACA others(5): Show |
T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0044 others(16): Show |
21 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.192-762_192-751del others(12): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910754 | ||||||
chr2:237910769 | TCA | T | 6 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0186 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-752_192-751del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910769 | ||||||
chr2:237910825 | TCACA | T | 5 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0186 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-700_192-697del others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910825 | ||||||
chr2:237910943 | TCACA | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0087 others(15): Show |
18 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.192-578_192-575del others(4): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237910943 | ||||||
chr2:237910956 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.192-572G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237910956 | |||||||
chr2:237911013 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192-515C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911013 | |||||||
chr2:237911033 | CTG | C | 4 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0234 others(1): Show |
4 | HG01891.hp2 HG02135.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-493_192-492del others(2): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237911033 | ||||||
chr2:237911157 | C | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0087 others(14): Show |
17 | HG01496.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.192-371C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911157 | |||||||
chr2:237911160 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192-368G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911160 | |||||||
chr2:237911237 | AT | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.192-288delT | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 237911237 | ||||||
chr2:237911240 | T | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(148): Show |
154 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.192-288T>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911240 | |||||||
chr2:237911372 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0191 a0001c0001t0001g0192 others(2): Show |
5 | HG01074.hp1 HG01192.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.192-156G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911372 | |||||||
chr2:237911403 | G | A | 13 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0142 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.192-125G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911403 | |||||||
chr2:237911406 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(49): Show |
54 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.192-122G>A | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911406 | |||||||
chr2:237911436 | C | T | 6 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0186 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.192-92C>T | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911436 | |||||||
chr2:237911488 | C | G | 1 | a0001c0002t0001g0375 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.192-40C>G | RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 2/2 | chr2 | 237911488 |