Item | Value |
---|---|
geneid | 220441 |
ensemblid | ENSG00000176641.11 |
hgncid | 26811 |
symbol | RNF152 |
name | ring finger protein 152 |
refseq_nuc | NM_173557.3 |
refseq_prot | NP_775828.1 |
ensembl_nuc | ENST00000312828.4 |
ensembl_prot | ENSP00000316628.3 |
mane_status | MANE Select |
chr | chr18 |
start | 61808067 |
end | 61893007 |
strand | - |
ver | v1.2 |
region | chr18:61808067-61893007 |
region5000 | chr18:61803067-61898007 |
regionname0 | RNF152_chr18_61808067_61893007 |
regionname5000 | RNF152_chr18_61803067_61898007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 203 | 308 | 85 | 51 | 128 | 14 | 28 | 96 | RNF152_chr18_61803067_61898007 | RNF152 | METLS others(198): Show |
chr18 | 61803067 | 61898007 |
a0002 | 0/0 | 203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | METLS others(198): Show |
chr18 | 61803067 | 61898007 |
a0003 | 0/0 | 203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | METLS others(198): Show |
chr18 | 61803067 | 61898007 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 609 | 247 | 59 | 43 | 112 | 11 | 21 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0001c0002 | 0/0 | 609 | 55 | 24 | 8 | 15 | 2 | 6 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0001c0003 | 0/1 | 609 | 3 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0001c0004 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0001c0006 | 0/0 | 609 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0001c0008 | 0/0 | 609 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0002c0007 | 0/0 | 609 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 | ||
a0003c0005 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ATGGA others(604): Show |
chr18 | 61803067 | 61898007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8747 | 45 | 4 | 3 | 37 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0002 | 0/0 | 8745 | 22 | 1 | 9 | 6 | 3 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0003 | 1/0 | 8745 | 21 | 7 | 3 | 7 | 1 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0004 | 0/0 | 8745 | 12 | 1 | 3 | 4 | 2 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0006 | 0/0 | 8746 | 10 | 1 | 2 | 6 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0007 | 0/0 | 8746 | 10 | 0 | 1 | 7 | 1 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0008 | 0/0 | 8748 | 6 | 0 | 2 | 3 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0010 | 0/0 | 8745 | 5 | 0 | 0 | 5 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0011 | 0/0 | 8745 | 5 | 4 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0012 | 0/0 | 8745 | 4 | 2 | 1 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0013 | 0/0 | 8746 | 4 | 2 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0014 | 0/0 | 8746 | 4 | 0 | 0 | 4 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0015 | 0/0 | 8743 | 4 | 3 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8738): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0019 | 0/0 | 8745 | 3 | 0 | 3 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0020 | 0/0 | 8746 | 3 | 0 | 2 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0021 | 0/0 | 8748 | 3 | 0 | 0 | 3 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0022 | 0/0 | 8746 | 3 | 2 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0027 | 0/0 | 8746 | 2 | 0 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0028 | 0/0 | 8745 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0029 | 0/0 | 8747 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0030 | 0/0 | 8746 | 2 | 0 | 0 | 1 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0031 | 0/0 | 8749 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8744): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0032 | 0/0 | 8754 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8749): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0033 | 0/0 | 8745 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0034 | 0/0 | 8745 | 2 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0035 | 0/0 | 8746 | 2 | 0 | 0 | 1 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0036 | 0/0 | 8745 | 2 | 0 | 2 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0037 | 0/0 | 8747 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0038 | 0/0 | 8746 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0039 | 0/0 | 8745 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0040 | 0/0 | 8744 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0041 | 0/0 | 8745 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0042 | 0/0 | 8746 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0043 | 0/0 | 8753 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0046 | 0/0 | 8746 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0070 | 0/0 | 8749 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8744): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0071 | 0/0 | 8749 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8744): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0072 | 0/0 | 8745 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0073 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0074 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0075 | 0/0 | 8747 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0076 | 0/0 | 8747 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0077 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0078 | 0/0 | 8748 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0079 | 0/0 | 8744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0080 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0081 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0082 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0083 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0084 | 0/0 | 8744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0085 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0086 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0087 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0088 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0089 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0090 | 0/0 | 8748 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0091 | 0/0 | 9067 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(9062): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0092 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0093 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0095 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0096 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0098 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0099 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0100 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0101 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0102 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0103 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8739): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0104 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8743): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0105 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0106 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0107 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0108 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0109 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0110 | 0/0 | 8746 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0111 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0112 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0113 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0114 | 0/0 | 8752 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8747): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0115 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0116 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0117 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0118 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0001t0119 | 0/0 | 8741 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8736): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0005 | 0/0 | 8753 | 12 | 1 | 2 | 5 | 1 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0009 | 0/0 | 8754 | 5 | 0 | 1 | 3 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8749): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0016 | 0/0 | 8752 | 3 | 2 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8747): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0017 | 0/0 | 8733 | 3 | 3 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8728): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0018 | 0/0 | 8754 | 3 | 2 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8749): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0023 | 0/0 | 8735 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8730): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0024 | 0/0 | 8751 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8746): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0025 | 0/0 | 8738 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8733): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0044 | 0/0 | 8766 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8761): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0045 | 0/0 | 8751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8746): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0047 | 0/0 | 8749 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8744): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0048 | 0/0 | 8751 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8746): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0049 | 0/0 | 8754 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8749): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0050 | 0/0 | 8753 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0051 | 0/0 | 8754 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8749): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0052 | 0/0 | 8755 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8750): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0053 | 0/0 | 8751 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8746): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0054 | 0/0 | 8752 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8747): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0055 | 0/0 | 8736 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8731): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0056 | 0/0 | 8733 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8728): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0057 | 0/0 | 8735 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8730): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0058 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8741): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0059 | 0/0 | 8753 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0060 | 0/0 | 8775 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8770): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0061 | 0/0 | 8773 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8768): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0062 | 0/0 | 8737 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8732): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0063 | 0/0 | 8767 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8762): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0064 | 0/0 | 8751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8746): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0065 | 0/0 | 8750 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8745): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0066 | 0/0 | 8753 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0002t0069 | 0/0 | 8753 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8748): Show |
chr18 | 61803067 | 61898007 |
a0001c0003t0026 | 0/0 | 8745 | 2 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0003t0067 | 0/1 | 8743 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8738): Show |
chr18 | 61803067 | 61898007 |
a0001c0004t0094 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0001c0006t0001 | 0/0 | 8747 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8742): Show |
chr18 | 61803067 | 61898007 |
a0001c0008t0004 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0002c0007t0097 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8740): Show |
chr18 | 61803067 | 61898007 |
a0003c0005t0068 | 0/0 | 8770 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | ACCCG others(8765): Show |
chr18 | 61803067 | 61898007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0012g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0012g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0013g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0014g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0014g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0014g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0015g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0019g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0019g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0019g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0020g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0020g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0020g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0021g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0021g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0022g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0022g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0022g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0027g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0027g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0028g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0028g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0029g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0029g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0030g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0031g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0031g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0032g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0032g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0033g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0033g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0034g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0034g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0035g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0035g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0036g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0036g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0037g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0037g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0038g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0038g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0039g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0039g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0040g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0040g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0041g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0041g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0042g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0042g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0043g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0043g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0046g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0070g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0071g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0072g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0073g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0074g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0075g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0076g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0077g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0078g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0079g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0080g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0081g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0082g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0083g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0084g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0085g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0086g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0087g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0088g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0089g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0090g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0091g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0092g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0093g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0095g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0096g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0098g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0099g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0100g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0101g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0102g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0103g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0104g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0105g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0106g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0107g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0108g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0109g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0110g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0111g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0112g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0113g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0114g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0115g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0116g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0117g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0118g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0001t0119g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0009g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0009g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0016g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0018g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0018g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0018g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0023g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0023g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0024g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0024g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0025g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0025g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0044g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0045g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0047g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0048g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0049g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0050g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0051g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0052g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0053g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0054g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0055g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0056g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0057g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0058g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0059g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0060g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0061g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0062g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0063g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0064g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0065g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0066g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0002t0069g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0003t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0003t0026g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0003t0067g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0004t0094g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0001c0008t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0002c0007t0097g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
a0003c0005t0068g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0072 | g0005 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0036 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0265 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00280 | hp1 | a0001 | c0003 | t0026 | g0282 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00323 | hp2 | a0001 | c0001 | t0030 | g0099 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00408 | hp2 | a0001 | c0001 | t0031 | g0192 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00423 | hp1 | a0001 | c0002 | t0009 | g0307 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00597 | hp1 | a0001 | c0002 | t0051 | g0014 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00597 | hp2 | a0001 | c0001 | t0008 | g0083 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00621 | hp1 | a0001 | c0001 | t0077 | g0225 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00621 | hp2 | a0001 | c0001 | t0118 | g0040 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00639 | hp1 | a0001 | c0001 | t0116 | g0239 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00639 | hp2 | a0001 | c0001 | t0013 | g0247 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00735 | hp2 | a0001 | c0002 | t0018 | g0079 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0109 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01070 | hp1 | a0001 | c0001 | t0019 | g0248 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01070 | hp2 | a0002 | c0007 | t0097 | g0266 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01071 | hp2 | a0001 | c0001 | t0019 | g0233 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01081 | hp2 | a0001 | c0001 | t0107 | g0037 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01099 | hp1 | a0001 | c0001 | t0085 | g0232 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01099 | hp2 | a0001 | c0001 | t0113 | g0003 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01106 | hp1 | a0001 | c0001 | t0083 | g0287 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0269 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0262 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01167 | hp1 | a0001 | c0002 | t0005 | g0226 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01175 | hp1 | a0001 | c0001 | t0020 | g0285 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01175 | hp2 | a0001 | c0001 | t0046 | g0026 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01192 | hp1 | a0001 | c0001 | t0020 | g0288 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01243 | hp1 | a0001 | c0001 | t0036 | g0267 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0163 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01255 | hp1 | a0001 | c0002 | t0063 | g0257 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01255 | hp2 | a0001 | c0001 | t0019 | g0245 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01258 | hp2 | a0001 | c0002 | t0060 | g0295 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01261 | hp1 | a0001 | c0002 | t0009 | g0228 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01261 | hp2 | a0001 | c0001 | t0110 | g0031 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01346 | hp2 | a0001 | c0001 | t0012 | g0264 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01433 | hp1 | a0001 | c0001 | t0036 | g0268 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01433 | hp2 | a0001 | c0001 | t0027 | g0255 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01517 | hp1 | a0001 | c0002 | t0009 | g0227 | EUR | IBS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01517 | hp2 | a0001 | c0001 | t0034 | g0196 | EUR | IBS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01884 | hp2 | a0001 | c0002 | t0017 | g0169 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0071 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01934 | hp1 | a0001 | c0002 | t0061 | g0296 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0132 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01943 | hp2 | a0001 | c0001 | t0080 | g0194 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01975 | hp2 | a0001 | c0002 | t0050 | g0195 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0234 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02055 | hp1 | a0001 | c0001 | t0038 | g0136 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02071 | hp1 | a0001 | c0008 | t0004 | g0064 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02080 | hp1 | a0001 | c0002 | t0016 | g0018 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02083 | hp1 | a0001 | c0001 | t0031 | g0090 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02083 | hp2 | a0001 | c0001 | t0070 | g0155 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02129 | hp2 | a0001 | c0001 | t0082 | g0291 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0063 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02132 | hp2 | a0001 | c0001 | t0086 | g0070 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02135 | hp1 | a0001 | c0001 | t0112 | g0151 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02145 | hp1 | a0001 | c0002 | t0045 | g0254 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02145 | hp2 | a0001 | c0001 | t0091 | g0213 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02155 | hp1 | a0001 | c0002 | t0009 | g0204 | EAS | CDX | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CDX | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02257 | hp1 | a0001 | c0002 | t0025 | g0133 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02257 | hp2 | a0001 | c0002 | t0058 | g0297 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02258 | hp1 | a0001 | c0001 | t0074 | g0212 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02258 | hp2 | a0001 | c0002 | t0062 | g0177 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02280 | hp1 | a0001 | c0002 | t0023 | g0171 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02280 | hp2 | a0001 | c0002 | t0005 | g0022 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02451 | hp1 | a0001 | c0001 | t0114 | g0159 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02451 | hp2 | a0001 | c0002 | t0024 | g0209 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02523 | hp1 | a0001 | c0002 | t0053 | g0218 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02572 | hp1 | a0001 | c0001 | t0089 | g0140 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02572 | hp2 | a0001 | c0001 | t0042 | g0281 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02602 | hp2 | a0001 | c0001 | t0013 | g0152 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0093 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02622 | hp1 | a0001 | c0002 | t0018 | g0186 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0165 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02630 | hp1 | a0001 | c0001 | t0043 | g0158 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02630 | hp2 | a0001 | c0001 | t0039 | g0183 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02647 | hp1 | a0001 | c0001 | t0037 | g0166 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02647 | hp2 | a0001 | c0001 | t0103 | g0068 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02683 | hp2 | a0001 | c0001 | t0040 | g0156 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02717 | hp1 | a0001 | c0001 | t0096 | g0303 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02717 | hp2 | a0001 | c0002 | t0057 | g0168 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02735 | hp1 | a0001 | c0002 | t0054 | g0131 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02735 | hp2 | a0001 | c0002 | t0005 | g0250 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02738 | hp1 | a0001 | c0001 | t0033 | g0117 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02809 | hp1 | a0001 | c0001 | t0117 | g0305 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0164 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02818 | hp1 | a0001 | c0002 | t0017 | g0172 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02818 | hp2 | a0001 | c0001 | t0111 | g0135 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02886 | hp1 | a0001 | c0003 | t0026 | g0041 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02886 | hp2 | a0001 | c0002 | t0023 | g0170 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02896 | hp1 | a0001 | c0001 | t0101 | g0174 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02897 | hp1 | a0001 | c0001 | t0073 | g0277 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02922 | hp1 | a0001 | c0001 | t0104 | g0181 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02922 | hp2 | a0001 | c0002 | t0055 | g0175 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02970 | hp1 | a0001 | c0001 | t0075 | g0211 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02970 | hp2 | a0001 | c0001 | t0022 | g0259 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02976 | hp1 | a0001 | c0002 | t0056 | g0167 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02976 | hp2 | a0001 | c0001 | t0043 | g0157 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03041 | hp1 | a0001 | c0001 | t0099 | g0138 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0261 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03098 | hp1 | a0003 | c0005 | t0068 | g0191 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03098 | hp2 | a0001 | c0004 | t0094 | g0252 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03130 | hp1 | a0001 | c0001 | t0034 | g0025 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03130 | hp2 | a0001 | c0001 | t0102 | g0180 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03139 | hp1 | a0001 | c0001 | t0088 | g0274 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0278 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03195 | hp1 | a0001 | c0001 | t0038 | g0137 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0198 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03453 | hp1 | a0001 | c0002 | t0059 | g0208 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03486 | hp1 | a0001 | c0001 | t0119 | g0260 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03486 | hp2 | a0001 | c0002 | t0018 | g0300 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03516 | hp1 | a0001 | c0001 | t0100 | g0078 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03516 | hp2 | a0001 | c0001 | t0115 | g0306 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03540 | hp1 | a0001 | c0002 | t0017 | g0173 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03579 | hp2 | a0001 | c0002 | t0066 | g0187 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03669 | hp1 | a0001 | c0001 | t0035 | g0053 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03704 | hp2 | a0001 | c0001 | t0033 | g0060 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03710 | hp1 | a0001 | c0002 | t0069 | g0189 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03710 | hp2 | a0001 | c0001 | t0076 | g0294 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03831 | hp1 | a0001 | c0002 | t0005 | g0017 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0293 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03834 | hp1 | a0001 | c0001 | t0040 | g0029 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03834 | hp2 | a0001 | c0002 | t0048 | g0292 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0067 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03942 | hp2 | a0001 | c0001 | t0020 | g0284 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG04115 | hp2 | a0001 | c0001 | t0027 | g0251 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG04204 | hp2 | a0001 | c0001 | t0071 | g0107 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0258 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18906 | hp1 | a0001 | c0002 | t0064 | g0253 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18906 | hp2 | a0001 | c0002 | t0025 | g0178 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18939 | hp1 | a0001 | c0002 | t0052 | g0015 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18942 | hp2 | a0001 | c0001 | t0010 | g0032 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18943 | hp1 | a0001 | c0001 | t0014 | g0298 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0052 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18944 | hp1 | a0001 | c0001 | t0028 | g0299 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18945 | hp1 | a0001 | c0002 | t0044 | g0095 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18946 | hp2 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0062 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18948 | hp2 | a0001 | c0001 | t0084 | g0143 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18949 | hp1 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18949 | hp2 | a0001 | c0001 | t0078 | g0215 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18951 | hp1 | a0001 | c0001 | t0087 | g0241 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18951 | hp2 | a0001 | c0001 | t0090 | g0021 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18956 | hp2 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18959 | hp1 | a0001 | c0001 | t0029 | g0206 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18959 | hp2 | a0001 | c0002 | t0005 | g0057 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18960 | hp2 | a0001 | c0001 | t0035 | g0273 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18964 | hp2 | a0001 | c0001 | t0106 | g0044 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18965 | hp1 | a0001 | c0001 | t0041 | g0048 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18965 | hp2 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18969 | hp2 | a0001 | c0002 | t0049 | g0205 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18972 | hp1 | a0001 | c0002 | t0005 | g0222 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0104 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18989 | hp2 | a0001 | c0002 | t0009 | g0308 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18990 | hp2 | a0001 | c0001 | t0029 | g0224 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18991 | hp1 | a0001 | c0001 | t0032 | g0125 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18991 | hp2 | a0001 | c0001 | t0032 | g0102 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18995 | hp1 | a0001 | c0001 | t0021 | g0115 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19000 | hp1 | a0001 | c0001 | t0092 | g0030 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19000 | hp2 | a0001 | c0001 | t0093 | g0129 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19003 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19009 | hp2 | a0001 | c0002 | t0005 | g0028 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19010 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19010 | hp2 | a0001 | c0001 | t0022 | g0272 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19030 | hp1 | a0001 | c0002 | t0016 | g0256 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0199 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19054 | hp1 | a0001 | c0001 | t0041 | g0049 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19057 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19062 | hp1 | a0001 | c0001 | t0008 | g0141 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19062 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19064 | hp1 | a0001 | c0001 | t0014 | g0238 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19064 | hp2 | a0001 | c0001 | t0079 | g0128 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19065 | hp1 | a0001 | c0001 | t0028 | g0045 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19067 | hp2 | a0001 | c0001 | t0007 | g0110 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19075 | hp1 | a0001 | c0001 | t0109 | g0229 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19075 | hp2 | a0001 | c0001 | t0030 | g0012 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19077 | hp2 | a0001 | c0001 | t0108 | g0242 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19078 | hp1 | a0001 | c0001 | t0105 | g0042 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19078 | hp2 | a0001 | c0001 | t0021 | g0074 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19085 | hp2 | a0001 | c0002 | t0005 | g0016 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19088 | hp2 | a0001 | c0002 | t0047 | g0221 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19240 | hp1 | a0001 | c0001 | t0095 | g0304 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0197 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0207 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0219 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20905 | hp1 | a0001 | c0002 | t0005 | g0230 | SAS | GIH | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20905 | hp2 | a0001 | c0006 | t0001 | g0153 | SAS | GIH | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0072 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02486 | hp1 | a0001 | c0002 | t0024 | g0210 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02486 | hp2 | a0001 | c0002 | t0065 | g0096 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02559 | hp1 | a0001 | c0001 | t0039 | g0184 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG02559 | hp2 | a0001 | c0001 | t0042 | g0280 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03471 | hp1 | a0001 | c0002 | t0016 | g0263 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0085 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG06807 | hp1 | a0001 | c0001 | t0098 | g0179 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
HG06807 | hp2 | a0001 | c0001 | t0081 | g0139 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
NA20300 | hp2 | a0001 | c0001 | t0037 | g0182 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
homoSapiens | chm13v2 | a0001 | c0003 | t0067 | g0283 | REF | REF | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0243 | REF | REF | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:61816015 | G | A | 1 | a0003 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.449C>T | p.Ala150Val | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 797/8745 | 449/612 | 150/203 | chr18 | 61816015 | |||
chr18:61816048 | T | C | 1 | a0002 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.416A>G | p.Gln139Arg | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 764/8745 | 416/612 | 139/203 | chr18 | 61816048 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:61815969 | G | C | 1 | a0001c0003 | 2 | HG00280.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.495C>G | p.Thr165Thr | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 843/8745 | 495/612 | 165/203 | chr18 | 61815969 | |||
chr18:61816077 | G | A | 1 | a0001c0003 | 2 | HG00280.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.387C>T | p.Ser129Ser | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 735/8745 | 387/612 | 129/203 | chr18 | 61816077 | |||
chr18:61816263 | C | T | 1 | a0001c0006 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.201G>A | p.Ser67Ser | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 549/8745 | 201/612 | 67/203 | chr18 | 61816263 | |||
chr18:61816275 | G | T | 1 | a0001c0003 | 2 | HG00280.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.189C>A | p.Gly63Gly | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 537/8745 | 189/612 | 63/203 | chr18 | 61816275 | |||
chr18:61816281 | A | G | 3 | a0001c0002 a0001c0003 a0003c0005 |
58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
synonymous_variant | LOW | c.183T>C | p.Pro61Pro | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 531/8745 | 183/612 | 61/203 | chr18 | 61816281 | |||
chr18:61816299 | G | A | 1 | a0001c0008 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.165C>T | p.Arg55Arg | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 513/8745 | 165/612 | 55/203 | chr18 | 61816299 | |||
chr18:61816455 | C | G | 1 | a0001c0004 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.9G>C | p.Thr3Thr | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 357/8745 | 9/612 | 3/203 | chr18 | 61816455 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:61808167 | C | T | 2 | a0001c0001t0019 a0001c0001t0027 |
5 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7685G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7685 | chr18 | 61808167 | ||||||
chr18:61808387 | T | TA | 23 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0008 others(20): Show |
57 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*7464dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAA | 4 | a0001c0002t0016 a0001c0002t0050 a0001c0002t0051 others(1): Show |
6 | HG00597.hp1 HG01975.hp2 HG02080.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7462_*7464dupTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAA | 9 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(6): Show |
21 | HG00741.hp1 HG01167.hp1 HG02280.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*7461_*7464dupTTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAAA | 7 | a0001c0002t0009 a0001c0002t0018 a0001c0002t0024 others(4): Show |
14 | HG00423.hp1 HG00735.hp2 HG01261.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7460_*7464dupTTTT others(1): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAAAAA others(6): Show |
1 | a0001c0002t0063 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7452_*7464dupTTTT others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAAAAA others(7): Show |
1 | a0003c0005t0068 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7451_*7464dupTTTT others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAAAAA others(14): Show |
2 | a0001c0002t0060 a0001c0002t0061 |
2 | HG01258.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7444_*7464dupTTTT others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | T | TAAAAAAA others(15): Show |
1 | a0001c0002t0044 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7443_*7464dupTTTT others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | ||||||
chr18:61808387 | TAAA | T | 4 | a0001c0002t0017 a0001c0002t0023 a0001c0002t0056 others(1): Show |
7 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7462_*7464delTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7462 | chr18 | 61808387 | ||||||
chr18:61808484 | A | T | 1 | a0001c0001t0085 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7368T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7368 | chr18 | 61808484 | ||||||
chr18:61808543 | G | A | 9 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0099 others(6): Show |
11 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7309C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7309 | chr18 | 61808543 | ||||||
chr18:61808563 | G | A | 22 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(19): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7289C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7289 | chr18 | 61808563 | ||||||
chr18:61808595 | A | T | 33 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(30): Show |
58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*7257T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7257 | chr18 | 61808595 | ||||||
chr18:61808935 | C | T | 1 | a0001c0002t0054 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6917G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6917 | chr18 | 61808935 | ||||||
chr18:61809202 | T | C | 22 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(19): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*6650A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6650 | chr18 | 61809202 | ||||||
chr18:61809236 | A | G | 33 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(30): Show |
58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6616T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6616 | chr18 | 61809236 | ||||||
chr18:61809349 | G | A | 1 | a0001c0001t0080 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6503 | chr18 | 61809349 | ||||||
chr18:61809425 | C | A | 1 | a0001c0001t0085 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6427G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6427 | chr18 | 61809425 | ||||||
chr18:61809747 | A | T | 1 | a0001c0001t0041 | 2 | NA18965.hp1 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6105T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6105 | chr18 | 61809747 | ||||||
chr18:61809856 | G | GA | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(36): Show |
92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*5995dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | ||||||
chr18:61809856 | G | GAA | 21 | a0001c0001t0022 a0001c0001t0075 a0001c0001t0077 others(18): Show |
43 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5994_*5995dupTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | ||||||
chr18:61809856 | GA | G | 9 | a0001c0001t0079 a0001c0001t0084 a0001c0001t0087 others(6): Show |
9 | HG02647.hp2 HG02896.hp1 HG03041.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5995delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | ||||||
chr18:61809856 | GAAAA | G | 6 | a0001c0002t0017 a0001c0002t0023 a0001c0002t0055 others(3): Show |
9 | HG01255.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5992_*5995delTTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5992 | chr18 | 61809856 | ||||||
chr18:61809882 | T | C | 1 | a0001c0001t0096 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5970A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5970 | chr18 | 61809882 | ||||||
chr18:61810026 | A | T | 32 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(29): Show |
57 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*5826T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5826 | chr18 | 61810026 | ||||||
chr18:61810029 | T | C | 22 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(19): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5823A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5823 | chr18 | 61810029 | ||||||
chr18:61810065 | C | T | 22 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(19): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5787G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5787 | chr18 | 61810065 | ||||||
chr18:61810180 | C | G | 3 | a0001c0001t0029 a0001c0001t0077 a0001c0001t0078 |
4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5672G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5672 | chr18 | 61810180 | ||||||
chr18:61810243 | A | C | 3 | a0001c0002t0044 a0001c0002t0060 a0001c0002t0061 |
3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5609T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5609 | chr18 | 61810243 | ||||||
chr18:61810272 | G | GGT | 29 | a0001c0001t0043 a0001c0001t0076 a0001c0001t0095 others(26): Show |
53 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5578_*5579dupAC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | ||||||
chr18:61810272 | G | GGTGTGTG others(3): Show |
2 | a0001c0002t0044 a0003c0005t0068 |
2 | HG03098.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5570_*5579dupACAC others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | ||||||
chr18:61810272 | G | GGTGTGTG others(7): Show |
1 | a0001c0002t0063 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5566_*5579dupACAC others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | ||||||
chr18:61810272 | G | GGTGTGTG others(11): Show |
1 | a0001c0002t0061 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5562_*5579dupACAC others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | ||||||
chr18:61810272 | G | GGTGTGTG others(13): Show |
1 | a0001c0002t0060 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5560_*5579dupACAC others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | ||||||
chr18:61810272 | GGTGT | G | 2 | a0001c0001t0015 a0001c0001t0119 |
5 | HG01109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5576_*5579delACAC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5576 | chr18 | 61810272 | ||||||
chr18:61810362 | T | A | 1 | a0001c0001t0082 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5490A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5490 | chr18 | 61810362 | ||||||
chr18:61810516 | C | T | 1 | a0002c0007t0097 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5336 | chr18 | 61810516 | ||||||
chr18:61810517 | G | A | 2 | a0001c0001t0095 a0001c0001t0096 |
2 | HG02717.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5335C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5335 | chr18 | 61810517 | ||||||
chr18:61810580 | G | A | 1 | a0003c0005t0068 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5272C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5272 | chr18 | 61810580 | ||||||
chr18:61810582 | A | C | 3 | a0001c0001t0012 a0001c0001t0020 a0001c0001t0083 |
8 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5270T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5270 | chr18 | 61810582 | ||||||
chr18:61810648 | C | CATAA | 2 | a0001c0001t0032 a0001c0001t0071 |
3 | HG04204.hp2 NA18991.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5200_*5203dupTTAT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5203 | chr18 | 61810648 | ||||||
chr18:61810710 | G | A | 2 | a0001c0001t0115 a0001c0001t0117 |
2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5142C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5142 | chr18 | 61810710 | ||||||
chr18:61810733 | C | A | 1 | a0001c0002t0069 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5119G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5119 | chr18 | 61810733 | ||||||
chr18:61810807 | T | C | 4 | a0001c0001t0037 a0001c0001t0098 a0001c0001t0102 others(1): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5045A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5045 | chr18 | 61810807 | ||||||
chr18:61810809 | T | C | 2 | a0001c0001t0036 a0002c0007t0097 |
3 | HG01070.hp2 HG01243.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5043A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5043 | chr18 | 61810809 | ||||||
chr18:61811047 | C | CA | 24 | a0001c0001t0043 a0001c0001t0088 a0001c0002t0005 others(21): Show |
46 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4804dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4804 | chr18 | 61811047 | ||||||
chr18:61811047 | CA | C | 24 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(21): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4804delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4804 | chr18 | 61811047 | ||||||
chr18:61811220 | C | T | 7 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0099 others(4): Show |
9 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4632G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4632 | chr18 | 61811220 | ||||||
chr18:61811221 | A | G | 22 | a0001c0001t0043 a0001c0001t0114 a0001c0002t0005 others(19): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4631T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4631 | chr18 | 61811221 | ||||||
chr18:61811256 | A | G | 1 | a0001c0002t0063 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4596T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4596 | chr18 | 61811256 | ||||||
chr18:61811471 | G | A | 1 | a0001c0001t0096 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4381C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4381 | chr18 | 61811471 | ||||||
chr18:61811547 | A | T | 1 | a0001c0001t0086 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4305T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4305 | chr18 | 61811547 | ||||||
chr18:61811568 | A | C | 1 | a0001c0001t0111 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4284T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4284 | chr18 | 61811568 | ||||||
chr18:61811611 | G | C | 1 | a0001c0001t0106 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4241 | chr18 | 61811611 | ||||||
chr18:61812089 | T | G | 2 | a0001c0001t0081 a0001c0001t0089 |
2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3763A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3763 | chr18 | 61812089 | ||||||
chr18:61812148 | G | A | 2 | a0001c0002t0056 a0001c0002t0057 |
2 | HG02717.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3704C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3704 | chr18 | 61812148 | ||||||
chr18:61812174 | T | A | 1 | a0003c0005t0068 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3678A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3678 | chr18 | 61812174 | ||||||
chr18:61812176 | G | A | 2 | a0001c0001t0115 a0001c0001t0117 |
2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3676C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3676 | chr18 | 61812176 | ||||||
chr18:61812180 | T | C | 1 | a0001c0001t0107 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3672A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3672 | chr18 | 61812180 | ||||||
chr18:61812286 | G | A | 2 | a0001c0001t0108 a0001c0001t0109 |
2 | NA19075.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3566C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3566 | chr18 | 61812286 | ||||||
chr18:61812378 | C | T | 1 | a0001c0001t0093 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3474G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3474 | chr18 | 61812378 | ||||||
chr18:61812593 | C | G | 4 | a0001c0001t0037 a0001c0001t0098 a0001c0001t0102 others(1): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3259G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3259 | chr18 | 61812593 | ||||||
chr18:61812597 | T | G | 4 | a0001c0001t0037 a0001c0001t0098 a0001c0001t0102 others(1): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3255A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3255 | chr18 | 61812597 | ||||||
chr18:61812768 | C | T | 1 | a0001c0003t0026 | 2 | HG00280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3084G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3084 | chr18 | 61812768 | ||||||
chr18:61812856 | CA | C | 32 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(29): Show |
57 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2995delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2995 | chr18 | 61812856 | ||||||
chr18:61812970 | G | C | 32 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(29): Show |
57 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2882C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2882 | chr18 | 61812970 | ||||||
chr18:61812994 | C | T | 32 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(29): Show |
57 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2858G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2858 | chr18 | 61812994 | ||||||
chr18:61813239 | C | A | 1 | a0001c0002t0049 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2613G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2613 | chr18 | 61813239 | ||||||
chr18:61813257 | T | TTC | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(13): Show |
71 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2593_*2594dupGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2594 | chr18 | 61813257 | ||||||
chr18:61813257 | T | TTCTC | 4 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0070 others(1): Show |
6 | HG00408.hp2 HG02083.hp1 HG02083.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2591_*2594dupGAGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2594 | chr18 | 61813257 | ||||||
chr18:61813257 | TTC | T | 5 | a0001c0002t0024 a0001c0002t0045 a0001c0002t0058 others(2): Show |
6 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2593_*2594delGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2593 | chr18 | 61813257 | ||||||
chr18:61813257 | TTCTC | T | 2 | a0001c0002t0023 a0001c0002t0057 |
3 | HG02280.hp1 HG02717.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2591_*2594delGAGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2591 | chr18 | 61813257 | ||||||
chr18:61813274 | TCTCTCA | T | 3 | a0001c0002t0017 a0001c0002t0055 a0001c0002t0056 |
5 | HG01884.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2577delTGAG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813274 | ||||||
chr18:61813274 | TCTCTCAC others(1): Show |
T | 2 | a0001c0002t0025 a0001c0002t0062 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2570_*2577delTGTG others(4): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813274 | ||||||
chr18:61813274 | TCTCTCAC others(3): Show |
T | 3 | a0001c0002t0044 a0001c0002t0060 a0001c0002t0061 |
3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2568_*2577delTGTG others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813274 | ||||||
chr18:61813276 | TCTCACA | T | 2 | a0001c0002t0018 a0001c0002t0066 |
3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2570_*2575delTGTG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813276 | ||||||
chr18:61813278 | T | A | 2 | a0001c0002t0018 a0001c0002t0059 |
2 | HG00735.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2574A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2574 | chr18 | 61813278 | ||||||
chr18:61813278 | T | TCA | 8 | a0001c0001t0072 a0001c0002t0005 a0001c0002t0009 others(5): Show |
21 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2573dupTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2573 | chr18 | 61813278 | ||||||
chr18:61813278 | T | TCACA | 3 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0053 |
4 | HG00423.hp1 HG02523.hp1 NA18989.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2570_*2573dupTGTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2573 | chr18 | 61813278 | ||||||
chr18:61813278 | TCA | T | 11 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0028 others(8): Show |
18 | HG01243.hp2 HG01255.hp1 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2573delTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813278 | ||||||
chr18:61813278 | TCACA | T | 28 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(25): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2570_*2573delTGTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813278 | ||||||
chr18:61813278 | TCACACA | T | 7 | a0001c0001t0043 a0001c0001t0073 a0001c0001t0099 others(4): Show |
8 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2568_*2573delTGTG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813278 | ||||||
chr18:61813278 | TCACACAC others(3): Show |
T | 1 | a0001c0003t0026 | 2 | HG00280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2564_*2573delTGTG others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2564 | chr18 | 61813278 | ||||||
chr18:61813280 | A | T | 39 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(36): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2572T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813280 | ||||||
chr18:61813282 | A | T | 30 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(27): Show |
66 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2570T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813282 | ||||||
chr18:61813284 | A | T | 38 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(35): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2568T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813284 | ||||||
chr18:61813286 | A | T | 37 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(34): Show |
88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2566T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2566 | chr18 | 61813286 | ||||||
chr18:61813288 | A | T | 31 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(28): Show |
78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2564T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2564 | chr18 | 61813288 | ||||||
chr18:61813309 | C | A | 14 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(11): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2543G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2543 | chr18 | 61813309 | ||||||
chr18:61813317 | T | C | 1 | a0001c0002t0053 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2535A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2535 | chr18 | 61813317 | ||||||
chr18:61813321 | CA | C | 3 | a0001c0002t0024 a0001c0002t0058 a0001c0002t0059 |
4 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2530 | chr18 | 61813321 | ||||||
chr18:61813343 | C | A | 1 | a0001c0003t0026 | 2 | HG00280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2509G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2509 | chr18 | 61813343 | ||||||
chr18:61813396 | C | T | 7 | a0001c0001t0010 a0001c0001t0092 a0001c0002t0017 others(4): Show |
14 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2456G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2456 | chr18 | 61813396 | ||||||
chr18:61813512 | T | TGGGATTG others(313): Show |
1 | a0001c0001t0091 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2339_*2340insGGCC others(316): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2339 | chr18 | 61813512 | ||||||
chr18:61813688 | T | C | 1 | a0001c0001t0033 | 2 | HG02738.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2164A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2164 | chr18 | 61813688 | ||||||
chr18:61813755 | C | T | 1 | a0001c0001t0072 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2097 | chr18 | 61813755 | ||||||
chr18:61813848 | T | C | 71 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(68): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2004A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2004 | chr18 | 61813848 | ||||||
chr18:61814007 | G | C | 2 | a0001c0001t0042 a0001c0001t0111 |
3 | HG02559.hp2 HG02572.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1845C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1845 | chr18 | 61814007 | ||||||
chr18:61814219 | C | T | 32 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(29): Show |
57 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1633G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1633 | chr18 | 61814219 | ||||||
chr18:61814225 | G | A | 1 | a0001c0002t0054 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1627 | chr18 | 61814225 | ||||||
chr18:61814316 | C | G | 12 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(9): Show |
29 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1536G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1536 | chr18 | 61814316 | ||||||
chr18:61814398 | G | C | 1 | a0001c0001t0112 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1454 | chr18 | 61814398 | ||||||
chr18:61814491 | G | A | 1 | a0001c0001t0113 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1361 | chr18 | 61814491 | ||||||
chr18:61814683 | C | A | 4 | a0001c0001t0043 a0001c0001t0114 a0001c0001t0115 others(1): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1169 | chr18 | 61814683 | ||||||
chr18:61814734 | C | T | 1 | a0001c0001t0071 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1118 | chr18 | 61814734 | ||||||
chr18:61814884 | G | C | 1 | a0001c0002t0069 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 968 | chr18 | 61814884 | ||||||
chr18:61814895 | G | A | 1 | a0001c0001t0011 | 5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 957 | chr18 | 61814895 | ||||||
chr18:61814913 | C | T | 1 | a0001c0001t0070 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 939 | chr18 | 61814913 | ||||||
chr18:61815050 | A | G | 33 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0016 others(30): Show |
58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*802T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 802 | chr18 | 61815050 | ||||||
chr18:61815053 | C | T | 1 | a0001c0001t0046 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 799 | chr18 | 61815053 | ||||||
chr18:61815074 | T | A | 1 | a0001c0001t0116 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 778 | chr18 | 61815074 | ||||||
chr18:61815077 | G | A | 1 | a0001c0001t0116 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 775 | chr18 | 61815077 | ||||||
chr18:61815197 | C | T | 1 | a0001c0002t0045 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 655 | chr18 | 61815197 | ||||||
chr18:61815685 | G | A | 1 | a0001c0001t0117 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 167 | chr18 | 61815685 | ||||||
chr18:61815743 | G | C | 1 | a0001c0001t0118 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 109 | chr18 | 61815743 | ||||||
chr18:61816485 | G | T | 1 | a0001c0002t0044 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 22 | chr18 | 61816485 | ||||||
chr18:61816530 | G | A | 2 | a0001c0001t0015 a0001c0001t0119 |
5 | HG01109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 67 | chr18 | 61816530 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:61816612 | A | G | 1 | a0001c0002t0044g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-135-14T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816612 | |||||||
chr18:61816765 | C | T | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-167G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816765 | |||||||
chr18:61816848 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0185 |
4 | NA18944.hp2 NA18964.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-250G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816848 | |||||||
chr18:61816969 | T | C | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-135-371A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816969 | |||||||
chr18:61817131 | C | G | 84 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-533G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817131 | |||||||
chr18:61817173 | G | A | 3 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0100g0078 |
3 | HG02055.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-135-575C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817173 | |||||||
chr18:61817190 | T | C | 2 | a0001c0003t0026g0041 a0001c0003t0026g0282 |
2 | HG00280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-135-592A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817190 | |||||||
chr18:61817437 | C | G | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-839G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817437 | |||||||
chr18:61817742 | T | TA | 51 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0043g0157 others(48): Show |
51 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-1145dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817742 | |||||||
chr18:61817742 | T | TAAA | 64 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-135-1147_-135-114 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817742 | |||||||
chr18:61817819 | G | A | 1 | a0001c0008t0004g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-1221C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817819 | |||||||
chr18:61817826 | C | T | 2 | a0001c0001t0081g0139 a0001c0001t0089g0140 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-135-1228G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817826 | |||||||
chr18:61817833 | C | T | 1 | a0001c0001t0012g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-135-1235G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817833 | |||||||
chr18:61817851 | G | A | 123 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-1253C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817851 | |||||||
chr18:61817874 | C | A | 2 | a0001c0002t0060g0295 a0001c0002t0061g0296 |
2 | HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-135-1276G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817874 | |||||||
chr18:61817925 | T | C | 6 | a0001c0001t0042g0280 a0001c0001t0042g0281 a0001c0001t0074g0212 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-1327A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817925 | |||||||
chr18:61817938 | T | A | 11 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(8): Show |
11 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-1340A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817938 | |||||||
chr18:61818021 | G | T | 123 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-1423C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818021 | |||||||
chr18:61818054 | T | C | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-1456A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818054 | |||||||
chr18:61818109 | A | C | 1 | a0001c0001t0076g0294 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-135-1511T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818109 | |||||||
chr18:61818259 | C | T | 3 | a0001c0002t0025g0133 a0001c0002t0025g0178 a0001c0002t0062g0177 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-1661G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818259 | |||||||
chr18:61818308 | G | A | 11 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(8): Show |
11 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-1710C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818308 | |||||||
chr18:61818705 | G | C | 11 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(8): Show |
11 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-2107C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818705 | |||||||
chr18:61818895 | G | A | 6 | a0001c0001t0004g0146 a0001c0001t0004g0203 a0001c0001t0004g0219 others(3): Show |
6 | HG00639.hp2 HG01106.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-2297C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818895 | |||||||
chr18:61818949 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0032g0102 |
2 | NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-135-2351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818949 | |||||||
chr18:61818966 | A | G | 11 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(8): Show |
11 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-2368T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818966 | |||||||
chr18:61818989 | C | G | 112 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-135-2391G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818989 | |||||||
chr18:61819032 | A | T | 1 | a0001c0002t0009g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-135-2434T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819032 | |||||||
chr18:61819066 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-135-2468G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819066 | |||||||
chr18:61819067 | G | A | 1 | a0001c0002t0018g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-135-2469C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819067 | |||||||
chr18:61819320 | G | A | 4 | a0001c0001t0029g0206 a0001c0001t0029g0224 a0001c0001t0077g0225 others(1): Show |
4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-2722C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819320 | |||||||
chr18:61819331 | C | T | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-2733G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819331 | |||||||
chr18:61819456 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-135-2858C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819456 | |||||||
chr18:61819499 | G | A | 1 | a0001c0001t0099g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-2901C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819499 | |||||||
chr18:61819554 | G | A | 2 | a0001c0003t0026g0041 a0001c0003t0026g0282 |
2 | HG00280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-135-2956C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819554 | |||||||
chr18:61819557 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-135-2959T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819557 | |||||||
chr18:61819744 | G | C | 4 | a0001c0001t0028g0299 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-3146C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819744 | |||||||
chr18:61819811 | A | G | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3213T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819811 | |||||||
chr18:61819842 | G | A | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-3244C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819842 | |||||||
chr18:61819854 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0004g0011 |
2 | HG02015.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-135-3256G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819854 | |||||||
chr18:61819857 | C | A | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-3259G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819857 | |||||||
chr18:61820020 | C | CA | 9 | a0001c0001t0001g0118 a0001c0001t0001g0220 a0001c0001t0002g0006 others(6): Show |
9 | HG01255.hp1 HG01981.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-135-3423dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820020 | |||||||
chr18:61820020 | CA | C | 49 | a0001c0001t0001g0246 a0001c0001t0003g0301 a0001c0001t0003g0302 others(46): Show |
49 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-135-3423delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820020 | |||||||
chr18:61820052 | G | A | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-3454C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820052 | |||||||
chr18:61820142 | A | C | 3 | a0001c0001t0002g0201 a0001c0001t0007g0067 a0001c0001t0040g0029 |
3 | HG03669.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-3544T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820142 | |||||||
chr18:61820180 | T | A | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-3582A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820180 | |||||||
chr18:61820236 | G | A | 1 | a0001c0001t0014g0298 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-135-3638C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820236 | |||||||
chr18:61820283 | C | G | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3685G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820283 | |||||||
chr18:61820308 | G | A | 5 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0098g0179 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-3710C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820308 | |||||||
chr18:61820322 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-3724G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820322 | |||||||
chr18:61820323 | C | T | 27 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(24): Show |
27 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-135-3725G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820323 | |||||||
chr18:61820328 | C | CA | 113 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0103 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-135-3731dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | |||||||
chr18:61820328 | CACCAAAA others(3): Show |
C | 6 | a0001c0001t0006g0004 a0001c0001t0043g0157 a0001c0001t0043g0158 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-3740_-135-373 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | |||||||
chr18:61820328 | CACCAAAA others(4): Show |
C | 4 | a0001c0001t0022g0259 a0001c0001t0022g0278 a0001c0001t0090g0021 others(1): Show |
4 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-3741_-135-373 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | |||||||
chr18:61820328 | CACCAAAA others(5): Show |
C | 1 | a0001c0001t0003g0240 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-135-3742_-135-373 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | |||||||
chr18:61820328 | CACCAAAA others(10): Show |
C | 1 | a0001c0001t0011g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-135-3747_-135-373 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | |||||||
chr18:61820330 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(177): Show |
182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-135-3732G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820330 | |||||||
chr18:61820331 | C | A | 113 | a0001c0001t0001g0061 a0001c0001t0001g0089 a0001c0001t0001g0103 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-135-3733G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | |||||||
chr18:61820331 | C | CAA | 22 | a0001c0001t0002g0027 a0001c0001t0002g0270 a0001c0001t0007g0108 others(19): Show |
22 | HG01071.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-3735_-135-373 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | |||||||
chr18:61820331 | CA | C | 6 | a0001c0001t0003g0217 a0001c0001t0003g0235 a0001c0001t0003g0236 others(3): Show |
6 | HG00639.hp1 HG01167.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-135-3734delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | |||||||
chr18:61820333 | A | C | 1 | a0001c0001t0087g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-135-3735T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820333 | |||||||
chr18:61820341 | A | C | 6 | a0001c0001t0006g0004 a0001c0001t0043g0157 a0001c0001t0043g0158 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-3743T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820341 | |||||||
chr18:61820342 | A | C | 4 | a0001c0001t0022g0259 a0001c0001t0022g0278 a0001c0001t0090g0021 others(1): Show |
4 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-3744T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820342 | |||||||
chr18:61820343 | A | C | 1 | a0001c0001t0003g0240 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-135-3745T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820343 | |||||||
chr18:61820348 | A | C | 1 | a0001c0001t0011g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-135-3750T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820348 | |||||||
chr18:61820502 | C | T | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-3904G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820502 | |||||||
chr18:61820515 | T | C | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3917A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820515 | |||||||
chr18:61820554 | C | T | 1 | a0001c0001t0106g0044 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-135-3956G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820554 | |||||||
chr18:61820666 | A | G | 2 | a0001c0001t0095g0304 a0001c0001t0096g0303 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-135-4068T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820666 | |||||||
chr18:61820674 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-135-4076A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820674 | |||||||
chr18:61820715 | C | T | 1 | a0001c0001t0034g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-135-4117G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820715 | |||||||
chr18:61820917 | C | T | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-4319G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820917 | |||||||
chr18:61820963 | G | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-4365C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820963 | |||||||
chr18:61821172 | C | T | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-4574G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821172 | |||||||
chr18:61821212 | G | C | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-4614C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821212 | |||||||
chr18:61821289 | C | T | 2 | a0001c0003t0026g0041 a0001c0003t0026g0282 |
2 | HG00280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-135-4691G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821289 | |||||||
chr18:61821325 | T | C | 1 | a0001c0001t0006g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-135-4727A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821325 | |||||||
chr18:61821348 | T | C | 3 | a0001c0002t0044g0095 a0001c0002t0060g0295 a0001c0002t0061g0296 |
3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-4750A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821348 | |||||||
chr18:61821397 | T | C | 1 | a0001c0001t0038g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-135-4799A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821397 | |||||||
chr18:61821430 | C | T | 5 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(2): Show |
5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-4832G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821430 | |||||||
chr18:61821456 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-135-4858C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821456 | |||||||
chr18:61821471 | A | G | 1 | a0001c0002t0044g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-135-4873T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821471 | |||||||
chr18:61821648 | C | T | 61 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-5050G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821648 | |||||||
chr18:61821869 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-135-5271G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821869 | |||||||
chr18:61821889 | C | T | 2 | a0001c0001t0019g0245 a0001c0001t0027g0255 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-135-5291G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821889 | |||||||
chr18:61821898 | A | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-5300T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821898 | |||||||
chr18:61821970 | G | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-5372C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821970 | |||||||
chr18:61822025 | A | G | 4 | a0001c0001t0029g0206 a0001c0001t0029g0224 a0001c0001t0077g0225 others(1): Show |
4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-5427T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822025 | |||||||
chr18:61822120 | C | T | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-5522G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822120 | |||||||
chr18:61822285 | A | C | 1 | a0001c0001t0002g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-135-5687T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822285 | |||||||
chr18:61822394 | A | G | 2 | a0001c0002t0005g0109 a0001c0002t0005g0226 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-135-5796T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822394 | |||||||
chr18:61822499 | G | A | 2 | a0001c0001t0004g0081 a0001c0001t0028g0045 |
2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-135-5901C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822499 | |||||||
chr18:61822501 | A | T | 11 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0042g0280 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-5903T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822501 | |||||||
chr18:61822512 | A | T | 1 | a0001c0002t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-135-5914T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822512 | |||||||
chr18:61822540 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-135-5942T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822540 | |||||||
chr18:61822597 | A | T | 1 | a0001c0001t0002g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-5999T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822597 | |||||||
chr18:61822805 | A | G | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-6207T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822805 | |||||||
chr18:61822900 | C | A | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6302G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822900 | |||||||
chr18:61822981 | C | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-6383G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822981 | |||||||
chr18:61823071 | G | C | 2 | a0001c0002t0045g0254 a0001c0002t0064g0253 |
2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-135-6473C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823071 | |||||||
chr18:61823253 | G | A | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6655C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823253 | |||||||
chr18:61823273 | T | C | 43 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(40): Show |
43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-135-6675A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823273 | |||||||
chr18:61823371 | C | G | 1 | a0001c0001t0087g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-135-6773G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823371 | |||||||
chr18:61823462 | AT | A | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-6865delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823462 | |||||||
chr18:61823488 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-135-6890T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823488 | |||||||
chr18:61823524 | C | G | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6926G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823524 | |||||||
chr18:61823535 | C | G | 44 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(41): Show |
44 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-135-6937G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823535 | |||||||
chr18:61823841 | G | A | 3 | a0001c0002t0025g0133 a0001c0002t0025g0178 a0001c0002t0062g0177 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-7243C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823841 | |||||||
chr18:61823862 | C | T | 1 | a0001c0001t0034g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-135-7264G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823862 | |||||||
chr18:61823883 | G | A | 1 | a0001c0001t0028g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-135-7285C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823883 | |||||||
chr18:61823901 | T | C | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-7303A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823901 | |||||||
chr18:61823923 | G | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-7325C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823923 | |||||||
chr18:61824139 | G | C | 2 | a0001c0002t0045g0254 a0001c0002t0064g0253 |
2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-135-7541C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824139 | |||||||
chr18:61824141 | G | A | 2 | a0001c0002t0023g0170 a0001c0002t0023g0171 |
2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-135-7543C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824141 | |||||||
chr18:61824186 | C | T | 11 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(8): Show |
11 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-7588G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824186 | |||||||
chr18:61824343 | T | C | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-7745A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824343 | |||||||
chr18:61824364 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-135-7766C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824364 | |||||||
chr18:61824431 | T | A | 17 | a0001c0001t0003g0142 a0001c0001t0003g0144 a0001c0001t0003g0149 others(14): Show |
17 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-135-7833A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824431 | |||||||
chr18:61824536 | T | C | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-7938A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824536 | |||||||
chr18:61824538 | G | T | 1 | a0001c0002t0016g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-135-7940C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824538 | |||||||
chr18:61824577 | T | C | 1 | a0001c0003t0026g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-135-7979A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824577 | |||||||
chr18:61824721 | C | T | 3 | a0001c0002t0044g0095 a0001c0002t0060g0295 a0001c0002t0061g0296 |
3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-8123G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824721 | |||||||
chr18:61824794 | A | T | 1 | a0001c0001t0013g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-8196T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824794 | |||||||
chr18:61824944 | T | C | 123 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-8346A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824944 | |||||||
chr18:61825116 | T | C | 2 | a0001c0001t0019g0245 a0001c0001t0027g0255 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-135-8518A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825116 | |||||||
chr18:61825381 | G | A | 1 | a0001c0002t0052g0015 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-135-8783C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825381 | |||||||
chr18:61825728 | G | T | 1 | a0001c0001t0117g0305 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-135-9130C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825728 | |||||||
chr18:61825740 | C | T | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-9142G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825740 | |||||||
chr18:61825836 | G | T | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-9238C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825836 | |||||||
chr18:61826019 | G | A | 1 | a0001c0001t0104g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-9421C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826019 | |||||||
chr18:61826101 | G | T | 69 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-9503C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826101 | |||||||
chr18:61826238 | C | G | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-135-9640G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826238 | |||||||
chr18:61826272 | A | G | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-135-9674T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826272 | |||||||
chr18:61826307 | C | T | 1 | a0001c0001t0021g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-135-9709G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826307 | |||||||
chr18:61826511 | T | G | 1 | a0001c0002t0065g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-9913A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826511 | |||||||
chr18:61826563 | C | CT | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-9966dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826563 | |||||||
chr18:61826579 | C | T | 15 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(12): Show |
15 | HG00280.hp1 HG01255.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-9981G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826579 | |||||||
chr18:61826743 | T | G | 1 | a0001c0001t0020g0284 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-135-10145A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826743 | |||||||
chr18:61826804 | C | T | 15 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(12): Show |
15 | HG00280.hp1 HG01255.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-10206G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826804 | |||||||
chr18:61826836 | C | T | 94 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-135-10238G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826836 | |||||||
chr18:61826857 | G | A | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-10259C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826857 | |||||||
chr18:61826973 | A | T | 7 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-10375T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826973 | |||||||
chr18:61827022 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0008g0293 a0001c0006t0001g0153 |
3 | HG00609.hp2 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-10424T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827022 | |||||||
chr18:61827032 | A | G | 79 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-135-10434T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827032 | |||||||
chr18:61827360 | C | G | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-10762G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827360 | |||||||
chr18:61827536 | G | A | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10938C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827536 | |||||||
chr18:61827592 | T | TTATA | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10998_-135-10 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827592 | |||||||
chr18:61827597 | G | T | 40 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10999C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827597 | |||||||
chr18:61827693 | A | G | 5 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0098g0179 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-11095T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827693 | |||||||
chr18:61827893 | C | T | 1 | a0001c0002t0054g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-135-11295G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827893 | |||||||
chr18:61828138 | C | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-11540G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828138 | |||||||
chr18:61828139 | G | A | 1 | a0001c0001t0013g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-11541C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828139 | |||||||
chr18:61828223 | T | C | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-11625A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828223 | |||||||
chr18:61828247 | CCTTT | C | 69 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-11653_-135-11 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828247 | |||||||
chr18:61828266 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-135-11668C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828266 | |||||||
chr18:61828295 | T | C | 142 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(139): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-135-11697A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828295 | |||||||
chr18:61828343 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-135-11745G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828343 | |||||||
chr18:61828373 | C | G | 86 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-135-11775G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828373 | |||||||
chr18:61828447 | C | T | 1 | a0001c0008t0004g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-11849G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828447 | |||||||
chr18:61828448 | G | A | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-11850C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828448 | |||||||
chr18:61828481 | G | A | 52 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0039g0183 others(49): Show |
52 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-135-11883C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828481 | |||||||
chr18:61828629 | G | GA | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12032dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828629 | |||||||
chr18:61828682 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-135-12084C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828682 | |||||||
chr18:61828932 | G | T | 69 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-12334C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828932 | |||||||
chr18:61829072 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-135-12474C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829072 | |||||||
chr18:61829236 | C | T | 1 | a0001c0002t0017g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-135-12638G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829236 | |||||||
chr18:61829254 | C | G | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-12656G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829254 | |||||||
chr18:61829472 | G | A | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-12874C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829472 | |||||||
chr18:61829504 | G | T | 44 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0071g0107 others(41): Show |
44 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-135-12906C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829504 | |||||||
chr18:61829506 | T | G | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12908A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829506 | |||||||
chr18:61829508 | T | G | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12910A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829508 | |||||||
chr18:61829510 | T | G | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12912A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829510 | |||||||
chr18:61829512 | T | G | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12914A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829512 | |||||||
chr18:61829568 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-12970A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829568 | |||||||
chr18:61829597 | G | GGAGA | 75 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-135-13003_-135-13 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | |||||||
chr18:61829597 | G | GGAGAGA | 36 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0002t0005g0016 others(33): Show |
36 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-135-13005_-135-13 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | |||||||
chr18:61829597 | G | GGAGAGAG others(1): Show |
5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-13007_-135-13 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | |||||||
chr18:61829597 | GGAGA | G | 7 | a0001c0002t0017g0172 a0001c0002t0017g0173 a0001c0002t0023g0170 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-13003_-135-13 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | |||||||
chr18:61829629 | T | A | 15 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0001t0043g0157 others(12): Show |
15 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-13031A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829629 | |||||||
chr18:61829637 | G | A | 34 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(31): Show |
34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-13039C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829637 | |||||||
chr18:61829764 | C | T | 34 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(31): Show |
34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-13166G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829764 | |||||||
chr18:61829820 | C | T | 5 | a0001c0001t0111g0135 a0001c0002t0018g0186 a0001c0002t0018g0300 others(2): Show |
5 | HG02622.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-13222G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829820 | |||||||
chr18:61829971 | G | C | 1 | a0001c0001t0007g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-13373C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829971 | |||||||
chr18:61830025 | C | CTT | 68 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-13429_-135-13 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830025 | |||||||
chr18:61830114 | C | T | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-13516G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830114 | |||||||
chr18:61830115 | G | A | 1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-13517C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830115 | |||||||
chr18:61830146 | C | T | 1 | a0001c0001t0080g0194 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-135-13548G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830146 | |||||||
chr18:61830170 | C | G | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13572G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830170 | |||||||
chr18:61830171 | A | G | 119 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-135-13573T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830171 | |||||||
chr18:61830278 | G | A | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13680C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830278 | |||||||
chr18:61830322 | A | G | 117 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-13724T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830322 | |||||||
chr18:61830530 | G | A | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-13932C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830530 | |||||||
chr18:61830562 | C | T | 123 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-13964G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830562 | |||||||
chr18:61830587 | G | A | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13989C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830587 | |||||||
chr18:61830607 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-135-14009A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830607 | |||||||
chr18:61830763 | A | AAGG | 85 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-14168_-135-14 others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830763 | |||||||
chr18:61830771 | T | C | 70 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-14173A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830771 | |||||||
chr18:61830909 | T | C | 40 | a0001c0001t0080g0194 a0001c0002t0005g0016 a0001c0002t0005g0017 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-14311A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830909 | |||||||
chr18:61831123 | C | A | 61 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14525G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831123 | |||||||
chr18:61831182 | G | A | 10 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0002t0017g0172 others(7): Show |
10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-14584C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831182 | |||||||
chr18:61831309 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-135-14711G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831309 | |||||||
chr18:61831321 | C | T | 1 | a0001c0001t0006g0269 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-135-14723G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831321 | |||||||
chr18:61831322 | G | A | 61 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14724C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831322 | |||||||
chr18:61831554 | G | A | 1 | a0001c0002t0061g0296 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-135-14956C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831554 | |||||||
chr18:61831680 | GAACA | G | 76 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-135-15086_-135-15 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831680 | |||||||
chr18:61831780 | TC | T | 76 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(73): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-135-15183delG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831780 | |||||||
chr18:61831915 | ATG | A | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(28): Show |
31 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-135-15319_-135-15 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831915 | |||||||
chr18:61831919 | GT | G | 4 | a0001c0002t0009g0228 a0001c0002t0024g0209 a0001c0002t0024g0210 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-15322delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831919 | |||||||
chr18:61831921 | GT | G | 69 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-15324delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831921 | |||||||
chr18:61831922 | T | G | 35 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(32): Show |
35 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-135-15324A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831922 | |||||||
chr18:61831922 | TG | T | 7 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-15325delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831922 | |||||||
chr18:61831943 | A | G | 1 | a0001c0002t0069g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-135-15345T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831943 | |||||||
chr18:61832002 | A | T | 10 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0002t0017g0172 others(7): Show |
10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-15404T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832002 | |||||||
chr18:61832161 | G | A | 1 | a0001c0001t0080g0194 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-135-15563C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832161 | |||||||
chr18:61832180 | T | C | 1 | a0001c0001t0012g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-135-15582A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832180 | |||||||
chr18:61832522 | T | G | 7 | a0001c0001t0003g0217 a0001c0001t0003g0237 a0001c0001t0003g0240 others(4): Show |
7 | HG02027.hp1 NA18943.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-15924A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832522 | |||||||
chr18:61832539 | G | C | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0132 |
3 | HG00280.hp2 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-135-15941C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832539 | |||||||
chr18:61832588 | T | C | 1 | a0001c0001t0040g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-135-15990A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832588 | |||||||
chr18:61832660 | T | A | 13 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0039g0183 others(10): Show |
13 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-135-16062A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832660 | |||||||
chr18:61832664 | C | T | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16066G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832664 | |||||||
chr18:61832679 | G | A | 67 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-16081C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832679 | |||||||
chr18:61832747 | C | T | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16149G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832747 | |||||||
chr18:61832755 | T | C | 1 | a0001c0001t0013g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-16157A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832755 | |||||||
chr18:61832949 | TAACATGG others(2): Show |
T | 5 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0098g0179 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-16360_-135-16 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832949 | |||||||
chr18:61833028 | C | G | 81 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-135-16430G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833028 | |||||||
chr18:61833076 | T | C | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16478A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833076 | |||||||
chr18:61833077 | G | A | 67 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-16479C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833077 | |||||||
chr18:61833107 | A | T | 55 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-135-16509T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833107 | |||||||
chr18:61833228 | A | C | 10 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0002t0017g0172 others(7): Show |
10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-16630T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833228 | |||||||
chr18:61833242 | G | T | 1 | a0001c0001t0013g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-135-16644C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833242 | |||||||
chr18:61833389 | C | A | 1 | a0001c0002t0005g0016 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-135-16791G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833389 | |||||||
chr18:61833408 | C | A | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16810G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833408 | |||||||
chr18:61833428 | A | G | 1 | a0001c0001t0012g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-135-16830T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833428 | |||||||
chr18:61833472 | C | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-16874G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833472 | |||||||
chr18:61833514 | G | A | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16916C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833514 | |||||||
chr18:61833566 | A | G | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-16968T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833566 | |||||||
chr18:61833569 | T | C | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16971A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833569 | |||||||
chr18:61833612 | C | T | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-17014G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833612 | |||||||
chr18:61833814 | G | A | 5 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0098g0179 others(2): Show |
5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-17216C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833814 | |||||||
chr18:61833829 | A | C | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17231T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833829 | |||||||
chr18:61833884 | TA | T | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17287delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833884 | |||||||
chr18:61833899 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(301): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-135-17301G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833899 | |||||||
chr18:61833904 | A | T | 68 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-17306T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833904 | |||||||
chr18:61833917 | T | A | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-17319A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833917 | |||||||
chr18:61833927 | T | C | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-17329A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833927 | |||||||
chr18:61833955 | T | C | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17357A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833955 | |||||||
chr18:61834114 | C | T | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17516G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834114 | |||||||
chr18:61834253 | A | G | 3 | a0001c0002t0025g0133 a0001c0002t0025g0178 a0001c0002t0062g0177 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-17655T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834253 | |||||||
chr18:61834266 | C | T | 10 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0002t0017g0172 others(7): Show |
10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-17668G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834266 | |||||||
chr18:61834519 | A | G | 68 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-17921T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834519 | |||||||
chr18:61834624 | A | G | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-18026T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834624 | |||||||
chr18:61834663 | T | G | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-18065A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834663 | |||||||
chr18:61834679 | AT | A | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-18082delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834679 | |||||||
chr18:61834718 | T | C | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-18120A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834718 | |||||||
chr18:61834779 | A | G | 14 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0001t0080g0194 others(11): Show |
14 | HG01255.hp1 HG01258.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-18181T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834779 | |||||||
chr18:61834791 | A | T | 2 | a0001c0001t0081g0139 a0001c0001t0089g0140 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-135-18193T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834791 | |||||||
chr18:61834913 | A | C | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-18315T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834913 | |||||||
chr18:61834988 | T | C | 68 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-18390A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834988 | |||||||
chr18:61835166 | C | T | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-18568G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835166 | |||||||
chr18:61835198 | T | G | 55 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-135-18600A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835198 | |||||||
chr18:61835208 | C | T | 8 | a0001c0002t0017g0172 a0001c0002t0017g0173 a0001c0002t0023g0170 others(5): Show |
8 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-18610G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835208 | |||||||
chr18:61835273 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-135-18675A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835273 | |||||||
chr18:61835292 | C | T | 1 | a0001c0001t0002g0007 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-135-18694G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835292 | |||||||
chr18:61835388 | C | T | 3 | a0001c0002t0005g0028 a0001c0002t0005g0222 a0001c0002t0047g0221 |
3 | NA18972.hp1 NA19009.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-135-18790G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835388 | |||||||
chr18:61835489 | G | A | 67 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-18891C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835489 | |||||||
chr18:61835612 | T | G | 116 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-19014A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835612 | |||||||
chr18:61835620 | A | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-19022T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835620 | |||||||
chr18:61835998 | C | A | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-19400G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835998 | |||||||
chr18:61836086 | C | A | 1 | a0001c0001t0104g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-19488G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836086 | |||||||
chr18:61836123 | G | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-19525C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836123 | |||||||
chr18:61836428 | T | C | 24 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0001t0038g0136 others(21): Show |
24 | HG01255.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.-135-19830A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836428 | |||||||
chr18:61836461 | G | C | 1 | a0001c0001t0071g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-135-19863C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836461 | |||||||
chr18:61836677 | C | A | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20079G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836677 | |||||||
chr18:61836685 | G | A | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20087C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836685 | |||||||
chr18:61836700 | T | C | 1 | a0001c0001t0043g0158 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-135-20102A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836700 | |||||||
chr18:61836727 | T | TA | 64 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-135-20130dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836727 | |||||||
chr18:61836862 | A | C | 3 | a0001c0002t0025g0133 a0001c0002t0025g0178 a0001c0002t0062g0177 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-20264T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836862 | |||||||
chr18:61836926 | G | A | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-20328C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836926 | |||||||
chr18:61836928 | C | A | 117 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-20330G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836928 | |||||||
chr18:61836969 | T | C | 1 | a0001c0001t0096g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-20371A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836969 | |||||||
chr18:61836997 | C | A | 2 | a0001c0001t0108g0242 a0001c0001t0109g0229 |
2 | NA19075.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-135-20399G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836997 | |||||||
chr18:61836997 | C | T | 34 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0022 others(31): Show |
34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-20399G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836997 | |||||||
chr18:61837116 | C | T | 35 | a0001c0001t0013g0164 a0001c0002t0005g0016 a0001c0002t0005g0017 others(32): Show |
35 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-135-20518G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837116 | |||||||
chr18:61837117 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(60): Show |
65 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-135-20519C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837117 | |||||||
chr18:61837308 | T | C | 1 | a0001c0001t0004g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-135-20710A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837308 | |||||||
chr18:61837327 | A | C | 130 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-135-20729T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837327 | |||||||
chr18:61837411 | G | A | 1 | a0001c0002t0023g0171 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-135-20813C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837411 | |||||||
chr18:61837426 | T | C | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-20828A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837426 | |||||||
chr18:61837426 | T | G | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20828A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837426 | |||||||
chr18:61837473 | C | T | 3 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 |
3 | HG02451.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-135-20875G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837473 | |||||||
chr18:61837881 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-135-21283C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837881 | |||||||
chr18:61838017 | AAC | A | 63 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-135-21421_-135-21 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838017 | |||||||
chr18:61838052 | C | T | 1 | a0001c0002t0017g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-135-21454G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838052 | |||||||
chr18:61838115 | A | G | 130 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-135-21517T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838115 | |||||||
chr18:61838326 | C | A | 4 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0060g0295 others(1): Show |
4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-21728G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838326 | |||||||
chr18:61838406 | C | A | 1 | a0001c0001t0028g0299 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-135-21808G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838406 | |||||||
chr18:61838407 | G | A | 1 | a0001c0001t0015g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-135-21809C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838407 | |||||||
chr18:61838529 | G | A | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-21931C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838529 | |||||||
chr18:61838564 | T | A | 119 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-135-21966A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838564 | |||||||
chr18:61838706 | C | T | 1 | a0001c0008t0004g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-22108G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838706 | |||||||
chr18:61838802 | C | T | 2 | a0001c0001t0038g0136 a0001c0001t0038g0137 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-135-22204G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838802 | |||||||
chr18:61839000 | G | A | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-22402C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839000 | |||||||
chr18:61839054 | C | CA | 8 | a0001c0001t0001g0116 a0001c0001t0001g0124 a0001c0001t0001g0289 others(5): Show |
8 | HG01433.hp2 HG01975.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-22457dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | |||||||
chr18:61839054 | CA | C | 56 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(53): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-135-22457delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | |||||||
chr18:61839054 | CAA | C | 33 | a0001c0001t0101g0174 a0001c0002t0005g0016 a0001c0002t0005g0017 others(30): Show |
33 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-135-22458_-135-22 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | |||||||
chr18:61839179 | T | C | 13 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0102g0180 others(10): Show |
13 | HG02280.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-135-22581A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839179 | |||||||
chr18:61839301 | C | G | 1 | a0001c0001t0032g0125 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-135-22703G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839301 | |||||||
chr18:61839385 | A | G | 22 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(19): Show |
22 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-22787T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839385 | |||||||
chr18:61839415 | G | C | 1 | a0001c0001t0107g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-135-22817C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839415 | |||||||
chr18:61839548 | G | T | 1 | a0001c0001t0007g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-135-22950C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839548 | |||||||
chr18:61839671 | G | A | 43 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.-135-23073C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839671 | |||||||
chr18:61839684 | G | A | 89 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-135-23086C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839684 | |||||||
chr18:61839714 | C | T | 90 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(87): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-135-23116G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839714 | |||||||
chr18:61839756 | G | A | 118 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-135-23158C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839756 | |||||||
chr18:61839757 | T | C | 3 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0003c0005t0068g0191 |
3 | HG03098.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-23159A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839757 | |||||||
chr18:61840056 | A | G | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23458T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840056 | |||||||
chr18:61840094 | A | G | 17 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0039g0183 others(14): Show |
17 | HG00735.hp2 HG01258.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-135-23496T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840094 | |||||||
chr18:61840209 | G | A | 1 | a0001c0002t0018g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-135-23611C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840209 | |||||||
chr18:61840374 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-135-23776A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840374 | |||||||
chr18:61840405 | T | C | 91 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-23807A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840405 | |||||||
chr18:61840479 | C | T | 5 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(2): Show |
5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23881G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840479 | |||||||
chr18:61840503 | T | A | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23905A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840503 | |||||||
chr18:61840611 | G | A | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-24013C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840611 | |||||||
chr18:61840813 | C | G | 1 | a0001c0001t0099g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-24215G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840813 | |||||||
chr18:61840875 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-135-24277A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840875 | |||||||
chr18:61840879 | C | T | 21 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0011g0066 others(18): Show |
21 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-135-24281G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840879 | |||||||
chr18:61840978 | A | C | 129 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-135-24380T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840978 | |||||||
chr18:61841064 | G | A | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-24466C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841064 | |||||||
chr18:61841104 | C | T | 3 | a0001c0002t0024g0209 a0001c0002t0024g0210 a0001c0002t0059g0208 |
3 | HG02451.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-135-24506G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841104 | |||||||
chr18:61841373 | C | T | 2 | a0001c0001t0012g0265 a0001c0001t0020g0285 |
2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-135-24775G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841373 | |||||||
chr18:61841471 | G | A | 117 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-24873C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841471 | |||||||
chr18:61841516 | A | C | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-24918T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841516 | |||||||
chr18:61841575 | T | A | 91 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-24977A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841575 | |||||||
chr18:61841642 | G | A | 117 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-25044C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841642 | |||||||
chr18:61841733 | C | G | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-25135G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841733 | |||||||
chr18:61841922 | T | C | 91 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-25324A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841922 | |||||||
chr18:61841947 | C | T | 117 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-25349G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841947 | |||||||
chr18:61842029 | A | G | 12 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0039g0183 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-135-25431T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842029 | |||||||
chr18:61842053 | A | T | 12 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0001t0039g0183 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-135-25455T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842053 | |||||||
chr18:61842126 | T | C | 1 | a0001c0002t0009g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-135-25528A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842126 | |||||||
chr18:61842271 | T | C | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-25673A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842271 | |||||||
chr18:61842347 | C | G | 1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-25749G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842347 | |||||||
chr18:61842474 | G | A | 94 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-135-25876C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842474 | |||||||
chr18:61842631 | G | A | 1 | a0001c0002t0065g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-26033C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842631 | |||||||
chr18:61842633 | G | A | 1 | a0001c0001t0076g0294 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-135-26035C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842633 | |||||||
chr18:61842732 | T | C | 1 | a0001c0002t0025g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-135-26134A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842732 | |||||||
chr18:61842749 | C | A | 3 | a0001c0002t0044g0095 a0001c0002t0060g0295 a0001c0002t0061g0296 |
3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-26151G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842749 | |||||||
chr18:61842775 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0098 |
3 | NA18944.hp2 NA19054.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-135-26177A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842775 | |||||||
chr18:61842953 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-135-26355C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842953 | |||||||
chr18:61843143 | C | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-26545G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843143 | |||||||
chr18:61843147 | T | TAAGTGCC others(35): Show |
2 | a0001c0001t0022g0272 a0001c0001t0035g0273 |
2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-135-26591_-135-26 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843147 | |||||||
chr18:61843211 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0103g0068 |
2 | HG00735.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-135-26613G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843211 | |||||||
chr18:61843327 | C | T | 118 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-135-26729G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843327 | |||||||
chr18:61843434 | G | A | 3 | a0001c0002t0024g0209 a0001c0002t0024g0210 a0001c0002t0059g0208 |
3 | HG02451.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-135-26836C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843434 | |||||||
chr18:61843448 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-135-26850C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843448 | |||||||
chr18:61843498 | C | T | 7 | a0001c0002t0017g0172 a0001c0002t0017g0173 a0001c0002t0023g0170 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-26900G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843498 | |||||||
chr18:61843510 | T | C | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-26912A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843510 | |||||||
chr18:61843558 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-135-26960G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843558 | |||||||
chr18:61843651 | G | A | 2 | a0001c0001t0022g0272 a0001c0001t0035g0273 |
2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-135-27053C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843651 | |||||||
chr18:61843655 | T | C | 1 | a0001c0001t0099g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-27057A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843655 | |||||||
chr18:61843797 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-135-27199C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843797 | |||||||
chr18:61843967 | T | C | 96 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-135-27369A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843967 | |||||||
chr18:61843978 | A | C | 7 | a0001c0001t0006g0056 a0001c0001t0010g0019 a0001c0001t0010g0032 others(4): Show |
7 | NA18942.hp2 NA18949.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-27380T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843978 | |||||||
chr18:61844077 | G | GGAAA | 48 | a0001c0001t0001g0061 a0001c0001t0001g0082 a0001c0001t0001g0088 others(45): Show |
48 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-135-27483_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(1): Show |
24 | a0001c0001t0001g0089 a0001c0001t0001g0185 a0001c0001t0001g0290 others(21): Show |
24 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-135-27487_-135-27 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(5): Show |
6 | a0001c0001t0001g0244 a0001c0001t0004g0146 a0001c0001t0007g0111 others(3): Show |
6 | HG00621.hp2 HG01106.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-27491_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(9): Show |
3 | a0001c0001t0001g0113 a0001c0001t0020g0288 a0001c0001t0039g0183 |
3 | HG01192.hp1 HG02630.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-135-27495_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(31): Show |
1 | a0001c0004t0094g0252 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(35): Show |
3 | a0001c0002t0005g0216 a0001c0002t0047g0221 a0001c0002t0069g0189 |
3 | HG03710.hp1 NA18956.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-135-27480_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(43): Show |
1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(56): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(43): Show |
1 | a0001c0002t0005g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(56): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(47): Show |
1 | a0001c0002t0024g0209 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(60): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(44): Show |
1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(57): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(36): Show |
1 | a0001c0002t0016g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(49): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(31): Show |
1 | a0001c0002t0005g0028 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | G | GGAAAGAA others(35): Show |
1 | a0001c0002t0005g0222 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | GGAAA | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0047 others(34): Show |
38 | HG00323.hp2 HG00408.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.-135-27483_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | GGAAAGAA others(1): Show |
G | 33 | a0001c0001t0001g0086 a0001c0001t0001g0112 a0001c0001t0001g0275 others(30): Show |
33 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-135-27487_-135-27 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | GGAAAGAA others(5): Show |
G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0130 others(11): Show |
15 | HG00280.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-27491_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | GGAAAGAA others(9): Show |
G | 6 | a0001c0001t0001g0098 a0001c0001t0003g0193 a0001c0001t0004g0176 others(3): Show |
6 | HG00597.hp2 HG02602.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-27495_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844077 | GGAAAGAA others(17): Show |
G | 2 | a0001c0001t0037g0182 a0001c0002t0017g0169 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-135-27503_-135-27 others(30): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | |||||||
chr18:61844078 | G | GAAAGAAA others(35): Show |
2 | a0001c0002t0005g0226 a0001c0002t0024g0210 |
2 | HG01167.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-135-27522_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844078 | |||||||
chr18:61844078 | G | GAAAGAAA others(39): Show |
1 | a0001c0002t0005g0109 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-135-27526_-135-27 others(52): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844078 | |||||||
chr18:61844082 | G | GAAAGAAA others(31): Show |
1 | a0001c0002t0009g0227 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-135-27522_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844082 | |||||||
chr18:61844082 | G | GAAAGAAA others(35): Show |
1 | a0001c0002t0059g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-135-27526_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844082 | |||||||
chr18:61844084 | A | AGAAAGAA others(30): Show |
1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-27487_-135-27 others(43): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844084 | |||||||
chr18:61844086 | G | A | 1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-27488C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844086 | |||||||
chr18:61844086 | G | GAAAGAAA others(31): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0162 |
2 | HG00738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-135-27526_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844086 | |||||||
chr18:61844098 | G | GAAAGAAA others(31): Show |
1 | a0001c0001t0010g0123 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-135-27538_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844098 | |||||||
chr18:61844103 | A | G | 1 | a0001c0001t0008g0069 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-135-27505T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844103 | |||||||
chr18:61844110 | G | GAA | 5 | a0001c0001t0006g0056 a0001c0001t0108g0242 a0001c0001t0109g0229 others(2): Show |
5 | HG00423.hp1 HG02486.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-27514_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844110 | |||||||
chr18:61844114 | G | GAA | 7 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0034 others(4): Show |
7 | HG00323.hp1 HG01167.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-27518_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844114 | |||||||
chr18:61844118 | G | GAA | 16 | a0001c0001t0002g0006 a0001c0001t0002g0020 a0001c0001t0002g0027 others(13): Show |
16 | HG00099.hp2 HG00408.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-135-27522_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844118 | |||||||
chr18:61844122 | G | GAA | 19 | a0001c0001t0002g0013 a0001c0001t0002g0039 a0001c0001t0002g0050 others(16): Show |
19 | HG00597.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-135-27526_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844122 | |||||||
chr18:61844126 | G | GAA | 3 | a0001c0001t0001g0024 a0001c0001t0007g0036 a0001c0001t0040g0029 |
3 | HG00140.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-135-27530_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844126 | |||||||
chr18:61844139 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0004g0081 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-135-27542_-135-27 others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844139 | |||||||
chr18:61844139 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0003g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-27542_-135-27 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844139 | |||||||
chr18:61844142 | T | G | 60 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27544A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844142 | |||||||
chr18:61844143 | T | A | 60 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27545A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844143 | |||||||
chr18:61844148 | G | A | 60 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27550C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844148 | |||||||
chr18:61844149 | A | AG | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27552_-135-27 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844149 | |||||||
chr18:61844150 | A | G | 57 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27552T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844150 | |||||||
chr18:61844153 | G | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27555C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844153 | |||||||
chr18:61844154 | G | A | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27556C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844154 | |||||||
chr18:61844157 | G | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27559C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844157 | |||||||
chr18:61844157 | G | T | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27559C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844157 | |||||||
chr18:61844158 | G | T | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27560C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844158 | |||||||
chr18:61844161 | G | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27563C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844161 | |||||||
chr18:61844162 | G | A | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27564C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | |||||||
chr18:61844162 | G | GAAATTAA | 18 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0027 others(15): Show |
18 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-27565_-135-27 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | |||||||
chr18:61844162 | G | T | 12 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0051 others(9): Show |
12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27564C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | |||||||
chr18:61844163 | G | A | 27 | a0001c0001t0001g0246 a0001c0001t0002g0008 a0001c0001t0002g0010 others(24): Show |
27 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-135-27565C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844163 | |||||||
chr18:61844163 | G | T | 12 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0051 others(9): Show |
12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27565C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844163 | |||||||
chr18:61844164 | AG | A | 3 | a0001c0001t0007g0067 a0001c0001t0015g0093 a0001c0002t0016g0018 |
3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27567delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844164 | |||||||
chr18:61844165 | G | A | 39 | a0001c0001t0001g0246 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
39 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.-135-27567C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844165 | |||||||
chr18:61844165 | G | GA | 18 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0027 others(15): Show |
18 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-27568_-135-27 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844165 | |||||||
chr18:61844166 | G | A | 21 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0027 others(18): Show |
21 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-135-27568C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | |||||||
chr18:61844166 | G | GAAAGAAA others(13): Show |
1 | a0001c0001t0002g0010 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-135-27569_-135-27 others(26): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | |||||||
chr18:61844166 | G | GAAATAAA others(9): Show |
1 | a0001c0001t0001g0246 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-135-27569_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | |||||||
chr18:61844166 | G | GAAATTAA others(5): Show |
25 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0023 others(22): Show |
25 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-135-27569_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | |||||||
chr18:61844166 | G | GAGAA | 12 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0051 others(9): Show |
12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27569_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | |||||||
chr18:61844170 | G | A | 25 | a0001c0001t0002g0043 a0001c0001t0002g0162 a0001c0001t0010g0123 others(22): Show |
25 | HG00738.hp1 HG00741.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-135-27572C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844170 | |||||||
chr18:61844171 | G | A | 60 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27573C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844171 | |||||||
chr18:61844176 | AGAGAGGA others(10): Show |
A | 19 | a0001c0001t0002g0043 a0001c0001t0002g0162 a0001c0001t0010g0123 others(16): Show |
19 | HG00738.hp1 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-135-27595_-135-27 others(23): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844176 | |||||||
chr18:61844178 | A | G | 61 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27580T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844178 | |||||||
chr18:61844186 | G | A | 61 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27588C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844186 | |||||||
chr18:61844187 | A | G | 61 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27589T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844187 | |||||||
chr18:61844187 | AAGGAAGG others(5): Show |
A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01081.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-135-27601_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844187 | |||||||
chr18:61844191 | A | AAGGGAAG others(5): Show |
14 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(11): Show |
14 | HG00735.hp2 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-27605_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844191 | |||||||
chr18:61844191 | A | AAGGGAAG others(17): Show |
11 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0012g0085 others(8): Show |
11 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-27617_-135-27 others(30): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844191 | |||||||
chr18:61844192 | AG | A | 61 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27595delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844192 | |||||||
chr18:61844203 | G | A | 1 | a0001c0001t0007g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27605C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844203 | |||||||
chr18:61844212 | A | AGGGAGGG others(12): Show |
1 | a0001c0001t0001g0188 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-135-27633_-135-27 others(25): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844212 | |||||||
chr18:61844216 | A | G | 1 | a0001c0001t0007g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27618T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844216 | |||||||
chr18:61844221 | A | G | 84 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-27623T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844221 | |||||||
chr18:61844223 | G | A | 84 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(81): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-27625C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844223 | |||||||
chr18:61844231 | C | T | 7 | a0001c0002t0017g0172 a0001c0002t0017g0173 a0001c0002t0023g0170 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-27633G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844231 | |||||||
chr18:61844255 | CCATAGTA others(3): Show |
C | 1 | a0001c0001t0007g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27667_-135-27 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844255 | |||||||
chr18:61844413 | A | G | 1 | a0001c0001t0004g0150 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-135-27815T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844413 | |||||||
chr18:61844426 | A | G | 82 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-135-27828T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844426 | |||||||
chr18:61844458 | G | A | 1 | a0001c0002t0061g0296 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-135-27860C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844458 | |||||||
chr18:61844798 | G | A | 2 | a0001c0001t0022g0259 a0001c0001t0022g0278 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-135-28200C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844798 | |||||||
chr18:61844870 | CA | C | 8 | a0001c0001t0001g0289 a0001c0001t0029g0206 a0001c0001t0029g0224 others(5): Show |
8 | HG00621.hp1 HG01255.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-28273delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844870 | |||||||
chr18:61844874 | A | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(77): Show |
82 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-135-28276T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844874 | |||||||
chr18:61844903 | C | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-28305G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844903 | |||||||
chr18:61844916 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0107g0037 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-135-28318C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844916 | |||||||
chr18:61844968 | C | T | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-28370G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844968 | |||||||
chr18:61844969 | A | G | 110 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-135-28371T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844969 | |||||||
chr18:61844975 | C | G | 1 | a0001c0008t0004g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-28377G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844975 | |||||||
chr18:61844977 | T | C | 1 | a0001c0001t0004g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-135-28379A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844977 | |||||||
chr18:61844994 | C | T | 2 | a0001c0001t0042g0280 a0001c0001t0042g0281 |
2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-135-28396G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844994 | |||||||
chr18:61844996 | C | T | 1 | a0001c0001t0008g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-135-28398G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844996 | |||||||
chr18:61845083 | T | C | 83 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-135-28485A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845083 | |||||||
chr18:61845437 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-28839C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845437 | |||||||
chr18:61845451 | C | T | 1 | a0001c0003t0026g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-135-28853G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845451 | |||||||
chr18:61845796 | C | G | 1 | a0001c0001t0104g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-29198G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845796 | |||||||
chr18:61845904 | C | G | 15 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0074g0212 others(12): Show |
15 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-29306G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845904 | |||||||
chr18:61845920 | T | TG | 13 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(10): Show |
13 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-135-29323dupC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845920 | |||||||
chr18:61845922 | G | T | 1 | a0001c0002t0069g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-135-29324C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845922 | |||||||
chr18:61845926 | G | T | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-29328C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845926 | |||||||
chr18:61845927 | GC | G | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-29330delG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845927 | |||||||
chr18:61845928 | C | G | 105 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(102): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-135-29330G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845928 | |||||||
chr18:61845930 | T | G | 51 | a0001c0001t0001g0046 a0001c0001t0001g0214 a0001c0001t0001g0220 others(48): Show |
51 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-29332A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845930 | |||||||
chr18:61845988 | A | G | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-29390T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845988 | |||||||
chr18:61846149 | T | C | 1 | a0001c0001t0007g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-135-29551A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846149 | |||||||
chr18:61846272 | C | A | 14 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0074g0212 others(11): Show |
14 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-29674G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846272 | |||||||
chr18:61846683 | G | C | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-30085C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846683 | |||||||
chr18:61846744 | T | C | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-30146A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846744 | |||||||
chr18:61846761 | C | T | 3 | a0001c0001t0036g0267 a0001c0001t0036g0268 a0002c0007t0097g0266 |
3 | HG01070.hp2 HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-135-30163G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846761 | |||||||
chr18:61846794 | A | T | 1 | a0001c0001t0004g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-135-30196T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846794 | |||||||
chr18:61846949 | C | T | 7 | a0001c0002t0005g0109 a0001c0002t0005g0207 a0001c0002t0005g0226 others(4): Show |
7 | HG00741.hp1 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-30351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846949 | |||||||
chr18:61847032 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-30434A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847032 | |||||||
chr18:61847083 | G | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-30485C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847083 | |||||||
chr18:61847090 | C | T | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-30492G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847090 | |||||||
chr18:61847151 | CAG | C | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-30555_-135-30 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847151 | |||||||
chr18:61847184 | T | C | 1 | a0001c0001t0028g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-135-30586A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847184 | |||||||
chr18:61847191 | A | G | 1 | a0001c0001t0104g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-30593T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847191 | |||||||
chr18:61847212 | T | A | 1 | a0001c0001t0015g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-135-30614A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847212 | |||||||
chr18:61847383 | G | C | 1 | a0001c0001t0020g0288 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-135-30785C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847383 | |||||||
chr18:61847600 | C | G | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-31002G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847600 | |||||||
chr18:61847613 | A | C | 1 | a0001c0001t0100g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-31015T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847613 | |||||||
chr18:61847750 | C | T | 110 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-135-31152G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847750 | |||||||
chr18:61848022 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-135-31424A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848022 | |||||||
chr18:61848105 | C | T | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-31507G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848105 | |||||||
chr18:61848162 | T | C | 7 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-31564A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848162 | |||||||
chr18:61848195 | A | G | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-31597T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848195 | |||||||
chr18:61848389 | G | A | 1 | a0001c0001t0033g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-135-31791C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848389 | |||||||
chr18:61848531 | G | A | 132 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(129): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-135-31933C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848531 | |||||||
chr18:61848537 | C | G | 1 | a0001c0001t0096g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-31939G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848537 | |||||||
chr18:61848558 | T | A | 1 | a0001c0001t0013g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-31960A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848558 | |||||||
chr18:61848604 | C | G | 22 | a0001c0001t0012g0085 a0001c0001t0012g0134 a0001c0001t0037g0166 others(19): Show |
22 | HG00735.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-32006G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848604 | |||||||
chr18:61848638 | C | T | 5 | a0001c0001t0080g0194 a0001c0002t0044g0095 a0001c0002t0050g0195 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-32040G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848638 | |||||||
chr18:61848962 | C | T | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0132 |
3 | HG00280.hp2 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-135-32364G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848962 | |||||||
chr18:61849087 | G | T | 1 | a0001c0001t0096g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-32489C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849087 | |||||||
chr18:61849101 | G | A | 11 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0095g0304 others(8): Show |
11 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-135-32503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849101 | |||||||
chr18:61849328 | A | C | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-32730T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849328 | |||||||
chr18:61849329 | A | C | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-32731T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849329 | |||||||
chr18:61849392 | A | G | 3 | a0001c0001t0001g0188 a0001c0001t0072g0005 a0001c0006t0001g0153 |
3 | HG00099.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-32794T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849392 | |||||||
chr18:61849517 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-135-32919G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849517 | |||||||
chr18:61849627 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0021g0115 |
2 | NA18969.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-135-33029T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849627 | |||||||
chr18:61849634 | A | G | 23 | a0001c0001t0001g0246 a0001c0001t0108g0242 a0001c0001t0109g0229 others(20): Show |
23 | HG00423.hp1 HG00741.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-135-33036T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849634 | |||||||
chr18:61849646 | A | G | 1 | a0001c0002t0059g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-135-33048T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849646 | |||||||
chr18:61849859 | G | A | 2 | a0001c0001t0095g0304 a0001c0001t0096g0303 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-135-33261C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849859 | |||||||
chr18:61849881 | T | C | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-33283A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849881 | |||||||
chr18:61849912 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-135-33314T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849912 | |||||||
chr18:61849957 | C | T | 1 | a0001c0001t0006g0269 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-135-33359G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849957 | |||||||
chr18:61850428 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0072g0005 a0001c0006t0001g0153 |
3 | HG00099.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-33830A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850428 | |||||||
chr18:61850469 | C | T | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-33871G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850469 | |||||||
chr18:61850508 | T | A | 1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-33910A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850508 | |||||||
chr18:61850563 | G | A | 1 | a0001c0001t0114g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-135-33965C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850563 | |||||||
chr18:61850571 | G | C | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-33973C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850571 | |||||||
chr18:61850652 | T | C | 132 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(129): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-135-34054A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850652 | |||||||
chr18:61850764 | C | T | 8 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0098g0179 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-34166G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850764 | |||||||
chr18:61850928 | G | A | 8 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0011g0197 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-34330C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850928 | |||||||
chr18:61850959 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-135-34361T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850959 | |||||||
chr18:61851042 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-135-34444G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851042 | |||||||
chr18:61851090 | T | TA | 18 | a0001c0001t0001g0112 a0001c0001t0006g0004 a0001c0001t0007g0077 others(15): Show |
18 | HG00735.hp2 HG01258.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-34493dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851090 | |||||||
chr18:61851090 | T | TAA | 20 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0037g0166 others(17): Show |
20 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-135-34494_-135-34 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851090 | |||||||
chr18:61851165 | C | A | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-135-34567G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851165 | |||||||
chr18:61851421 | G | A | 24 | a0001c0001t0037g0166 a0001c0001t0037g0182 a0001c0001t0038g0136 others(21): Show |
24 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-135-34823C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851421 | |||||||
chr18:61851425 | G | T | 1 | a0001c0002t0065g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-34827C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851425 | |||||||
chr18:61851507 | T | C | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-34909A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851507 | |||||||
chr18:61851718 | T | C | 79 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-135-35120A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851718 | |||||||
chr18:61851787 | T | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-35189A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851787 | |||||||
chr18:61851787 | T | C | 45 | a0001c0001t0003g0190 a0001c0001t0003g0193 a0001c0001t0003g0200 others(42): Show |
45 | HG00735.hp2 HG01243.hp2 HG01258.hp2 others(42): Show |
intron_variant | MODIFIER | c.-135-35189A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851787 | |||||||
chr18:61852066 | G | T | 9 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0011g0197 others(6): Show |
9 | HG02615.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-135-35468C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852066 | |||||||
chr18:61852101 | G | A | 34 | a0001c0001t0001g0246 a0001c0001t0029g0206 a0001c0001t0029g0224 others(31): Show |
34 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-135-35503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852101 | |||||||
chr18:61852256 | T | G | 138 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(135): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-135-35658A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852256 | |||||||
chr18:61852324 | G | A | 6 | a0001c0001t0074g0212 a0001c0001t0075g0211 a0001c0001t0091g0213 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-35726C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852324 | |||||||
chr18:61852397 | G | A | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0002t0025g0133 |
3 | HG02257.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-135-35799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852397 | |||||||
chr18:61852521 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0007g0076 |
2 | NA18945.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-135-35923G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852521 | |||||||
chr18:61852553 | T | C | 51 | a0001c0001t0001g0246 a0001c0001t0003g0193 a0001c0001t0003g0200 others(48): Show |
51 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-35955A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852553 | |||||||
chr18:61852810 | C | A | 1 | a0001c0001t0021g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-135-36212G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852810 | |||||||
chr18:61852932 | A | G | 3 | a0001c0001t0039g0183 a0001c0001t0039g0184 a0001c0002t0058g0297 |
3 | HG02257.hp2 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-135-36334T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852932 | |||||||
chr18:61853127 | C | T | 135 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0006 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-135-36529G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853127 | |||||||
chr18:61853296 | C | CT | 32 | a0001c0001t0001g0091 a0001c0001t0002g0010 a0001c0001t0002g0038 others(29): Show |
32 | HG00735.hp1 HG00735.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.-135-36699dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853296 | |||||||
chr18:61853296 | C | CTT | 56 | a0001c0001t0001g0024 a0001c0001t0002g0006 a0001c0001t0002g0007 others(53): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-135-36700_-135-36 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853296 | |||||||
chr18:61853353 | G | A | 3 | a0001c0002t0048g0292 a0001c0002t0060g0295 a0001c0002t0061g0296 |
3 | HG01258.hp2 HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-135-36755C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853353 | |||||||
chr18:61853470 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-135-36872A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853470 | |||||||
chr18:61853541 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-135-36943G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853541 | |||||||
chr18:61853559 | C | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-36961G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853559 | |||||||
chr18:61853814 | T | C | 7 | a0001c0001t0076g0294 a0001c0001t0080g0194 a0001c0002t0044g0095 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-37216A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853814 | |||||||
chr18:61853859 | C | T | 1 | a0001c0001t0096g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-37261G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853859 | |||||||
chr18:61853874 | G | A | 17 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(14): Show |
17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-135-37276C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853874 | |||||||
chr18:61854102 | C | T | 2 | a0001c0001t0100g0078 a0001c0002t0018g0079 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-135-37504G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854102 | |||||||
chr18:61854116 | G | C | 1 | a0001c0001t0010g0123 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-135-37518C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854116 | |||||||
chr18:61854178 | C | A | 17 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(14): Show |
17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-135-37580G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854178 | |||||||
chr18:61854211 | T | C | 1 | a0001c0001t0033g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-135-37613A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854211 | |||||||
chr18:61854339 | G | GTTTTCCC others(2): Show |
3 | a0001c0001t0029g0206 a0001c0001t0029g0224 a0001c0001t0078g0215 |
3 | NA18949.hp2 NA18959.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-135-37742_-135-37 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854339 | |||||||
chr18:61854410 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-135-37812T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854410 | |||||||
chr18:61854433 | G | A | 77 | a0001c0001t0001g0024 a0001c0001t0001g0214 a0001c0001t0002g0006 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-135-37835C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854433 | |||||||
chr18:61854457 | T | A | 11 | a0001c0001t0001g0246 a0001c0001t0108g0242 a0001c0001t0109g0229 others(8): Show |
11 | HG00423.hp1 HG02155.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-135-37859A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854457 | |||||||
chr18:61854551 | G | A | 1 | a0001c0002t0056g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-135-37953C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854551 | |||||||
chr18:61854846 | A | G | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+37949T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854846 | |||||||
chr18:61854917 | A | T | 34 | a0001c0001t0001g0246 a0001c0001t0012g0085 a0001c0001t0012g0134 others(31): Show |
34 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-136+37878T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854917 | |||||||
chr18:61855041 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(73): Show |
78 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-136+37754T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855041 | |||||||
chr18:61855082 | C | T | 1 | a0001c0001t0076g0294 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-136+37713G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855082 | |||||||
chr18:61855332 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(71): Show |
76 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-136+37463A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855332 | |||||||
chr18:61855406 | G | A | 32 | a0001c0001t0001g0246 a0001c0001t0029g0206 a0001c0001t0029g0224 others(29): Show |
32 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+37389C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855406 | |||||||
chr18:61855422 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+37373C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855422 | |||||||
chr18:61855676 | CCCACACT others(6): Show |
C | 1 | a0001c0001t0031g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-136+37106_-136+37 others(19): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855676 | |||||||
chr18:61855765 | G | A | 1 | a0001c0001t0008g0071 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-136+37030C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855765 | |||||||
chr18:61855851 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+36944G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855851 | |||||||
chr18:61855957 | C | T | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+36838G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855957 | |||||||
chr18:61855997 | A | G | 1 | a0001c0002t0063g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+36798T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855997 | |||||||
chr18:61856209 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(72): Show |
77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+36586C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856209 | |||||||
chr18:61856267 | A | G | 1 | a0001c0003t0026g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-136+36528T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856267 | |||||||
chr18:61856293 | G | A | 2 | a0001c0001t0080g0194 a0001c0002t0050g0195 |
2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-136+36502C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856293 | |||||||
chr18:61856392 | C | T | 19 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0082 others(16): Show |
19 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+36403G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856392 | |||||||
chr18:61856466 | T | C | 5 | a0001c0001t0043g0157 a0001c0001t0043g0158 a0001c0001t0114g0159 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+36329A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856466 | |||||||
chr18:61856517 | C | G | 1 | a0001c0002t0016g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136+36278G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856517 | |||||||
chr18:61856602 | G | A | 2 | a0001c0001t0039g0183 a0001c0001t0039g0184 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+36193C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856602 | |||||||
chr18:61856995 | C | T | 1 | a0001c0001t0028g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-136+35800G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856995 | |||||||
chr18:61857028 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(81): Show |
86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-136+35767C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857028 | |||||||
chr18:61857079 | C | T | 32 | a0001c0001t0001g0246 a0001c0001t0029g0206 a0001c0001t0029g0224 others(29): Show |
32 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+35716G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857079 | |||||||
chr18:61857095 | C | T | 4 | a0001c0001t0003g0080 a0001c0001t0003g0092 a0001c0001t0015g0093 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+35700G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857095 | |||||||
chr18:61857160 | C | T | 8 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(5): Show |
8 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+35635G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857160 | |||||||
chr18:61857203 | C | T | 1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+35592G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857203 | |||||||
chr18:61857217 | A | C | 17 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(14): Show |
17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+35578T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857217 | |||||||
chr18:61857410 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0047 others(81): Show |
86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-136+35385C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857410 | |||||||
chr18:61857427 | T | C | 1 | a0001c0001t0111g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-136+35368A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857427 | |||||||
chr18:61857630 | G | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+35165C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857630 | |||||||
chr18:61857694 | TAAAC | T | 38 | a0001c0001t0001g0246 a0001c0001t0029g0206 a0001c0001t0029g0224 others(35): Show |
38 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136+35097_-136+35 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857694 | |||||||
chr18:61857760 | A | C | 1 | a0001c0004t0094g0252 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-136+35035T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857760 | |||||||
chr18:61857981 | C | T | 27 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(24): Show |
27 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-136+34814G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857981 | |||||||
chr18:61858036 | G | C | 1 | a0001c0001t0095g0304 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-136+34759C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858036 | |||||||
chr18:61858077 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0013g0152 a0001c0001t0072g0005 others(1): Show |
4 | HG00099.hp1 HG02602.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+34718G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858077 | |||||||
chr18:61858194 | T | C | 1 | a0001c0001t0028g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-136+34601A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858194 | |||||||
chr18:61858415 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+34380G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858415 | |||||||
chr18:61858612 | G | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+34183C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858612 | |||||||
chr18:61858906 | A | G | 2 | a0001c0001t0038g0136 a0001c0001t0038g0137 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-136+33889T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858906 | |||||||
chr18:61858973 | T | C | 1 | a0001c0002t0049g0205 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-136+33822A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858973 | |||||||
chr18:61858986 | G | A | 1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+33809C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858986 | |||||||
chr18:61859010 | GA | G | 17 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(14): Show |
17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+33784delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859010 | |||||||
chr18:61859018 | A | G | 4 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0095g0304 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+33777T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859018 | |||||||
chr18:61859126 | C | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+33669G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859126 | |||||||
chr18:61859301 | G | A | 1 | a0001c0001t0087g0241 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-136+33494C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859301 | |||||||
chr18:61859364 | G | A | 3 | a0001c0002t0017g0169 a0001c0002t0023g0170 a0001c0002t0023g0171 |
3 | HG01884.hp2 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-136+33431C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859364 | |||||||
chr18:61859390 | G | A | 44 | a0001c0001t0001g0246 a0001c0001t0003g0193 a0001c0001t0003g0200 others(41): Show |
44 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-136+33405C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859390 | |||||||
chr18:61859391 | G | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(62): Show |
67 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-136+33404C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859391 | |||||||
chr18:61859880 | A | AAAAAG | 9 | a0001c0001t0038g0136 a0001c0001t0038g0137 a0001c0002t0017g0169 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+32910_-136+32 others(11): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | |||||||
chr18:61859880 | A | AAAAAGAA others(3): Show |
8 | a0001c0001t0037g0182 a0001c0001t0039g0184 a0001c0001t0098g0179 others(5): Show |
8 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+32905_-136+32 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | |||||||
chr18:61859880 | A | AAAAAGAA others(8): Show |
8 | a0001c0001t0039g0183 a0001c0001t0099g0138 a0001c0001t0101g0174 others(5): Show |
8 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+32900_-136+32 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | |||||||
chr18:61859880 | A | AAAAAGAA others(13): Show |
2 | a0001c0002t0025g0178 a0001c0002t0062g0177 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-136+32895_-136+32 others(26): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | |||||||
chr18:61859980 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+32815A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859980 | |||||||
chr18:61860030 | C | T | 2 | a0001c0001t0038g0136 a0001c0001t0038g0137 |
2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-136+32765G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860030 | |||||||
chr18:61860034 | A | C | 2 | a0001c0001t0036g0267 a0001c0001t0036g0268 |
2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-136+32761T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860034 | |||||||
chr18:61860037 | ACAGAAAA others(4): Show |
A | 1 | a0001c0002t0005g0230 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+32747_-136+32 others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860037 | |||||||
chr18:61860284 | T | C | 2 | a0001c0001t0007g0110 a0001c0001t0007g0111 |
2 | NA18946.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-136+32511A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860284 | |||||||
chr18:61860382 | G | A | 10 | a0001c0001t0101g0174 a0001c0002t0017g0169 a0001c0002t0017g0172 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+32413C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860382 | |||||||
chr18:61860523 | G | A | 29 | a0001c0001t0001g0246 a0001c0001t0029g0206 a0001c0001t0029g0224 others(26): Show |
29 | HG00423.hp1 HG00621.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-136+32272C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860523 | |||||||
chr18:61860558 | A | G | 90 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0214 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-136+32237T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860558 | |||||||
chr18:61860734 | T | C | 1 | a0001c0001t0006g0062 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-136+32061A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860734 | |||||||
chr18:61860745 | G | C | 30 | a0001c0001t0001g0246 a0001c0001t0002g0043 a0001c0001t0029g0206 others(27): Show |
30 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-136+32050C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860745 | |||||||
chr18:61860928 | T | A | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+31867A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860928 | |||||||
chr18:61861189 | T | C | 16 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(13): Show |
16 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136+31606A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861189 | |||||||
chr18:61861194 | TCCACTCA | T | 10 | a0001c0001t0101g0174 a0001c0002t0017g0169 a0001c0002t0017g0172 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+31594_-136+31 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861194 | |||||||
chr18:61861219 | C | T | 3 | a0001c0002t0018g0186 a0001c0002t0018g0300 a0001c0002t0066g0187 |
3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-136+31576G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861219 | |||||||
chr18:61861350 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-136+31445A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861350 | |||||||
chr18:61861444 | C | T | 44 | a0001c0001t0001g0246 a0001c0001t0002g0201 a0001c0001t0003g0193 others(41): Show |
44 | HG00423.hp1 HG00621.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.-136+31351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861444 | |||||||
chr18:61861481 | C | A | 100 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0214 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.-136+31314G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861481 | |||||||
chr18:61861541 | C | G | 10 | a0001c0001t0002g0201 a0001c0001t0003g0193 a0001c0001t0003g0200 others(7): Show |
10 | HG01346.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136+31254G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861541 | |||||||
chr18:61861752 | C | G | 1 | a0001c0001t0111g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-136+31043G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861752 | |||||||
chr18:61861757 | A | C | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31038T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861757 | |||||||
chr18:61861759 | C | G | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31036G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861759 | |||||||
chr18:61861760 | A | G | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31035T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861760 | |||||||
chr18:61861802 | G | C | 1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+30993C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861802 | |||||||
chr18:61861940 | A | C | 17 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(14): Show |
17 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-136+30855T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861940 | |||||||
chr18:61862195 | C | T | 44 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-136+30600G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862195 | |||||||
chr18:61862348 | T | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0112 a0001c0001t0001g0121 others(2): Show |
5 | NA18939.hp2 NA18948.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+30447A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862348 | |||||||
chr18:61862534 | A | C | 1 | a0001c0001t0082g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136+30261T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862534 | |||||||
chr18:61862544 | G | A | 3 | a0001c0001t0004g0054 a0001c0001t0004g0058 a0001c0001t0004g0059 |
3 | HG00280.hp2 HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-136+30251C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862544 | |||||||
chr18:61862546 | TA | T | 8 | a0001c0001t0011g0066 a0001c0001t0011g0163 a0001c0001t0013g0164 others(5): Show |
8 | HG00735.hp2 HG01243.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+30248delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862546 | |||||||
chr18:61862586 | C | G | 1 | a0001c0001t0033g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-136+30209G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862586 | |||||||
chr18:61862633 | T | C | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0002t0025g0133 |
3 | HG02257.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-136+30162A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862633 | |||||||
chr18:61862681 | A | C | 5 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+30114T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862681 | |||||||
chr18:61862695 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+30100G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862695 | |||||||
chr18:61862755 | G | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+30040C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862755 | |||||||
chr18:61862783 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(4): Show |
7 | HG01975.hp1 HG02523.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+30012C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862783 | |||||||
chr18:61862828 | C | T | 1 | a0001c0001t0082g0291 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136+29967G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862828 | |||||||
chr18:61862849 | T | C | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+29946A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862849 | |||||||
chr18:61863254 | G | A | 58 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0220 others(55): Show |
58 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-136+29541C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863254 | |||||||
chr18:61863263 | T | C | 1 | a0001c0001t0099g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-136+29532A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863263 | |||||||
chr18:61863296 | G | A | 1 | a0001c0001t0112g0151 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-136+29499C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863296 | |||||||
chr18:61863307 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-136+29488G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863307 | |||||||
chr18:61863313 | T | C | 2 | a0001c0001t0081g0139 a0001c0001t0089g0140 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+29482A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863313 | |||||||
chr18:61863366 | T | C | 14 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(11): Show |
14 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+29429A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863366 | |||||||
chr18:61863429 | G | A | 3 | a0001c0001t0039g0183 a0001c0001t0039g0184 a0001c0001t0103g0068 |
3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+29366C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863429 | |||||||
chr18:61863433 | C | CA | 38 | a0001c0001t0001g0089 a0001c0001t0001g0118 a0001c0001t0002g0201 others(35): Show |
38 | HG01255.hp1 HG01346.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.-136+29361dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | |||||||
chr18:61863433 | CA | C | 89 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0119 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-136+29361delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | |||||||
chr18:61863433 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0088 a0001c0001t0093g0129 |
2 | HG00609.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-136+29352_-136+29 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | |||||||
chr18:61863482 | C | T | 2 | a0001c0001t0015g0258 a0001c0002t0063g0257 |
2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+29313G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863482 | |||||||
chr18:61863834 | C | T | 1 | a0001c0001t0112g0151 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-136+28961G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863834 | |||||||
chr18:61863930 | C | T | 103 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0220 others(100): Show |
103 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-136+28865G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863930 | |||||||
chr18:61863974 | C | T | 204 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-136+28821G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863974 | |||||||
chr18:61864017 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+28778A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864017 | |||||||
chr18:61864123 | C | T | 4 | a0001c0001t0006g0269 a0001c0001t0036g0267 a0001c0001t0036g0268 others(1): Show |
4 | HG01070.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+28672G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864123 | |||||||
chr18:61864164 | C | T | 2 | a0001c0001t0041g0048 a0001c0001t0041g0049 |
2 | NA18965.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-136+28631G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864164 | |||||||
chr18:61864269 | A | G | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+28526T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864269 | |||||||
chr18:61864289 | C | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+28506G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864289 | |||||||
chr18:61864298 | C | T | 1 | a0001c0001t0004g0150 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-136+28497G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864298 | |||||||
chr18:61864574 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-136+28221A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864574 | |||||||
chr18:61864680 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-136+28115C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864680 | |||||||
chr18:61864700 | C | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+28095G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864700 | |||||||
chr18:61864739 | G | T | 12 | a0001c0001t0101g0174 a0001c0001t0115g0306 a0001c0001t0117g0305 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+28056C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864739 | |||||||
chr18:61864770 | G | A | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+28025C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864770 | |||||||
chr18:61864780 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+28015G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864780 | |||||||
chr18:61864784 | C | T | 6 | a0001c0001t0015g0261 a0001c0001t0015g0262 a0001c0001t0022g0259 others(3): Show |
6 | HG01109.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+28011G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864784 | |||||||
chr18:61864836 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27959A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864836 | |||||||
chr18:61864845 | C | T | 3 | a0001c0001t0003g0080 a0001c0001t0003g0092 a0001c0001t0015g0093 |
3 | HG02615.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-136+27950G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864845 | |||||||
chr18:61864847 | C | T | 1 | a0001c0001t0033g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-136+27948G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864847 | |||||||
chr18:61864996 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864996 | |||||||
chr18:61865296 | G | C | 3 | a0001c0001t0028g0045 a0001c0001t0090g0021 a0001c0001t0106g0044 |
3 | NA18951.hp2 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-136+27499C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865296 | |||||||
chr18:61865417 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+27378C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865417 | |||||||
chr18:61865440 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27355T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865440 | |||||||
chr18:61865494 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27301A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865494 | |||||||
chr18:61865525 | G | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+27270C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865525 | |||||||
chr18:61865525 | G | C | 1 | a0001c0001t0104g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-136+27270C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865525 | |||||||
chr18:61865527 | A | C | 1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+27268T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865527 | |||||||
chr18:61865628 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136+27167G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865628 | |||||||
chr18:61865643 | G | C | 7 | a0001c0001t0074g0212 a0001c0001t0075g0211 a0001c0001t0091g0213 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+27152C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865643 | |||||||
chr18:61865720 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-136+27075A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865720 | |||||||
chr18:61866323 | C | T | 1 | a0001c0002t0017g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-136+26472G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866323 | |||||||
chr18:61866422 | A | C | 5 | a0001c0001t0002g0201 a0001c0001t0003g0202 a0001c0001t0004g0203 others(2): Show |
5 | HG01346.hp1 HG02145.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+26373T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866422 | |||||||
chr18:61866459 | C | T | 1 | a0001c0001t0088g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136+26336G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866459 | |||||||
chr18:61866460 | G | A | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+26335C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866460 | |||||||
chr18:61866546 | C | G | 2 | a0001c0001t0073g0277 a0003c0005t0068g0191 |
2 | HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-136+26249G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866546 | |||||||
chr18:61866548 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(72): Show |
77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+26247G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866548 | |||||||
chr18:61866554 | T | C | 11 | a0001c0001t0073g0277 a0001c0001t0101g0174 a0001c0002t0017g0169 others(8): Show |
11 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-136+26241A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866554 | |||||||
chr18:61866653 | C | T | 4 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0095g0304 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+26142G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866653 | |||||||
chr18:61866687 | A | G | 20 | a0001c0001t0008g0293 a0001c0001t0037g0182 a0001c0001t0038g0136 others(17): Show |
20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+26108T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866687 | |||||||
chr18:61866752 | G | A | 1 | a0001c0001t0037g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136+26043C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866752 | |||||||
chr18:61866797 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-136+25998G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866797 | |||||||
chr18:61866896 | C | G | 12 | a0001c0001t0101g0174 a0001c0001t0115g0306 a0001c0001t0117g0305 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+25899G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866896 | |||||||
chr18:61866901 | C | CA | 32 | a0001c0001t0001g0188 a0001c0001t0001g0214 a0001c0001t0002g0162 others(29): Show |
32 | HG00423.hp2 HG00438.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+25893dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866901 | |||||||
chr18:61866961 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-136+25834C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866961 | |||||||
chr18:61867143 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-136+25652A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867143 | |||||||
chr18:61867335 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-136+25460A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867335 | |||||||
chr18:61867452 | A | C | 1 | a0001c0002t0016g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-136+25343T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867452 | |||||||
chr18:61867537 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(72): Show |
77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+25258T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867537 | |||||||
chr18:61867566 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-136+25229A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867566 | |||||||
chr18:61867596 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+25199C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867596 | |||||||
chr18:61867651 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+25144C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867651 | |||||||
chr18:61867657 | A | C | 1 | a0001c0001t0031g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136+25138T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867657 | |||||||
chr18:61867794 | A | G | 15 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0088 others(12): Show |
15 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136+25001T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867794 | |||||||
chr18:61867903 | C | T | 15 | a0001c0001t0012g0264 a0001c0001t0012g0265 a0001c0001t0020g0284 others(12): Show |
15 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136+24892G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867903 | |||||||
chr18:61867925 | C | T | 91 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0214 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-136+24870G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867925 | |||||||
chr18:61867950 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24845T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867950 | |||||||
chr18:61868079 | G | T | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+24716C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868079 | |||||||
chr18:61868183 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24612C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868183 | |||||||
chr18:61868195 | A | G | 97 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.-136+24600T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868195 | |||||||
chr18:61868213 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(72): Show |
77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+24582A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868213 | |||||||
chr18:61868340 | C | G | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+24455G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868340 | |||||||
chr18:61868364 | C | A | 1 | a0001c0001t0021g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-136+24431G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868364 | |||||||
chr18:61868445 | G | A | 20 | a0001c0001t0008g0293 a0001c0001t0037g0182 a0001c0001t0038g0136 others(17): Show |
20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+24350C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868445 | |||||||
chr18:61868519 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24276C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868519 | |||||||
chr18:61868560 | G | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+24235C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868560 | |||||||
chr18:61868608 | C | T | 2 | a0001c0002t0005g0222 a0001c0002t0047g0221 |
2 | NA18972.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-136+24187G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868608 | |||||||
chr18:61868658 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24137T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868658 | |||||||
chr18:61868715 | T | TA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(65): Show |
70 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-136+24079dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868715 | |||||||
chr18:61868985 | G | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23810C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868985 | |||||||
chr18:61869036 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23759A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869036 | |||||||
chr18:61869058 | C | T | 5 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0011g0197 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+23737G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869058 | |||||||
chr18:61869120 | C | T | 2 | a0001c0001t0012g0085 a0001c0001t0012g0134 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-136+23675G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869120 | |||||||
chr18:61869284 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23511A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869284 | |||||||
chr18:61869472 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23323A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869472 | |||||||
chr18:61869778 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+23017G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869778 | |||||||
chr18:61869897 | C | A | 2 | a0001c0001t0019g0245 a0001c0001t0027g0255 |
2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-136+22898G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869897 | |||||||
chr18:61870091 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+22704C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870091 | |||||||
chr18:61870308 | G | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+22487C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870308 | |||||||
chr18:61870455 | A | C | 30 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-136+22340T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870455 | |||||||
chr18:61870490 | C | T | 3 | a0001c0001t0039g0183 a0001c0001t0039g0184 a0001c0001t0103g0068 |
3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+22305G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870490 | |||||||
chr18:61870742 | T | A | 1 | a0001c0001t0007g0077 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-136+22053A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870742 | |||||||
chr18:61870879 | C | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(211): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-136+21916G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870879 | |||||||
chr18:61870880 | C | A | 95 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.-136+21915G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870880 | |||||||
chr18:61870914 | C | T | 1 | a0001c0001t0006g0147 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-136+21881G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870914 | |||||||
chr18:61870973 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+21822G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870973 | |||||||
chr18:61871078 | T | G | 5 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+21717A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871078 | |||||||
chr18:61871092 | C | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+21703G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871092 | |||||||
chr18:61871216 | A | C | 1 | a0001c0001t0021g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-136+21579T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871216 | |||||||
chr18:61871221 | A | T | 1 | a0001c0001t0008g0071 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-136+21574T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871221 | |||||||
chr18:61871301 | C | T | 4 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0095g0304 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+21494G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871301 | |||||||
chr18:61871416 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+21379A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871416 | |||||||
chr18:61871551 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0004g0219 a0001c0001t0006g0004 others(1): Show |
4 | HG00639.hp2 HG01981.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+21244G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871551 | |||||||
chr18:61871607 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-136+21188A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871607 | |||||||
chr18:61871707 | C | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-136+21088G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871707 | |||||||
chr18:61871776 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+21019G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871776 | |||||||
chr18:61871861 | A | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20934T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871861 | |||||||
chr18:61871892 | T | C | 6 | a0001c0001t0012g0264 a0001c0001t0012g0265 a0001c0001t0020g0284 others(3): Show |
6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+20903A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871892 | |||||||
chr18:61871907 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20888T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871907 | |||||||
chr18:61871989 | A | G | 19 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+20806T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871989 | |||||||
chr18:61872057 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20738G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872057 | |||||||
chr18:61872061 | T | C | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+20734A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872061 | |||||||
chr18:61872118 | T | A | 30 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-136+20677A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872118 | |||||||
chr18:61872193 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0034g0025 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-136+20602T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872193 | |||||||
chr18:61872410 | A | G | 1 | a0001c0001t0008g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-136+20385T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872410 | |||||||
chr18:61872425 | G | A | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20370C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872425 | |||||||
chr18:61872541 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20254T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872541 | |||||||
chr18:61872542 | T | C | 20 | a0001c0001t0008g0293 a0001c0001t0037g0182 a0001c0001t0038g0136 others(17): Show |
20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+20253A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872542 | |||||||
chr18:61872614 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-136+20181A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872614 | |||||||
chr18:61872689 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20106A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872689 | |||||||
chr18:61872779 | G | C | 1 | a0001c0001t0003g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-136+20016C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872779 | |||||||
chr18:61872931 | T | G | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+19864A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872931 | |||||||
chr18:61872942 | G | C | 1 | a0001c0001t0004g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-136+19853C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872942 | |||||||
chr18:61873043 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19752A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873043 | |||||||
chr18:61873046 | G | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19749C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873046 | |||||||
chr18:61873105 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19690A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873105 | |||||||
chr18:61873118 | T | C | 1 | a0001c0001t0022g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136+19677A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873118 | |||||||
chr18:61873233 | A | G | 1 | a0001c0001t0086g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-136+19562T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873233 | |||||||
chr18:61873311 | C | T | 1 | a0001c0002t0053g0218 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+19484G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873311 | |||||||
chr18:61873313 | C | A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.-136+19482G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873313 | |||||||
chr18:61873336 | T | C | 1 | a0001c0001t0010g0123 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-136+19459A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873336 | |||||||
chr18:61873441 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-136+19354C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873441 | |||||||
chr18:61873614 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19181T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873614 | |||||||
chr18:61873620 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0004g0081 |
2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-136+19175G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873620 | |||||||
chr18:61873877 | C | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+18918G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873877 | |||||||
chr18:61873962 | C | T | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+18833G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873962 | |||||||
chr18:61874346 | C | T | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+18449G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874346 | |||||||
chr18:61874347 | G | A | 6 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0055 others(3): Show |
6 | HG00408.hp1 NA18943.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+18448C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874347 | |||||||
chr18:61874425 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18370G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874425 | |||||||
chr18:61874443 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+18352C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874443 | |||||||
chr18:61874476 | C | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18319G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874476 | |||||||
chr18:61874476 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0008g0069 |
2 | NA18965.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-136+18319G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874476 | |||||||
chr18:61874477 | A | G | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18318T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874477 | |||||||
chr18:61874523 | A | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18272T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874523 | |||||||
chr18:61874594 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18201G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874594 | |||||||
chr18:61874742 | G | T | 1 | a0001c0001t0012g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-136+18053C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874742 | |||||||
chr18:61875022 | T | C | 8 | a0001c0002t0017g0169 a0001c0002t0017g0172 a0001c0002t0017g0173 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+17773A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875022 | |||||||
chr18:61875135 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+17660C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875135 | |||||||
chr18:61875264 | G | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17531C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875264 | |||||||
chr18:61875283 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17512G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875283 | |||||||
chr18:61875409 | G | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17386C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875409 | |||||||
chr18:61875454 | T | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17341A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875454 | |||||||
chr18:61875495 | C | A | 2 | a0001c0001t0100g0078 a0001c0002t0018g0079 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-136+17300G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875495 | |||||||
chr18:61875572 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0006g0062 a0001c0001t0032g0125 |
3 | NA18948.hp1 NA18991.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-136+17223G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875572 | |||||||
chr18:61875581 | T | TA | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17213_-136+17 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875581 | |||||||
chr18:61875635 | C | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17160G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875635 | |||||||
chr18:61875776 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-136+17019C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875776 | |||||||
chr18:61875787 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-136+17008G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875787 | |||||||
chr18:61875944 | C | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+16851G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875944 | |||||||
chr18:61876032 | T | C | 2 | a0001c0001t0022g0272 a0001c0001t0035g0273 |
2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-136+16763A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876032 | |||||||
chr18:61876152 | A | G | 2 | a0001c0001t0080g0194 a0001c0002t0050g0195 |
2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-136+16643T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876152 | |||||||
chr18:61876184 | G | A | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+16611C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876184 | |||||||
chr18:61876197 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(74): Show |
79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+16598A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876197 | |||||||
chr18:61876662 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+16133A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876662 | |||||||
chr18:61876745 | C | T | 114 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-136+16050G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876745 | |||||||
chr18:61876779 | C | T | 1 | a0001c0001t0099g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-136+16016G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876779 | |||||||
chr18:61876801 | G | A | 1 | a0001c0001t0007g0076 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-136+15994C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876801 | |||||||
chr18:61876907 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-136+15888C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876907 | |||||||
chr18:61877110 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-136+15685G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877110 | |||||||
chr18:61877111 | G | A | 3 | a0001c0001t0003g0142 a0001c0001t0003g0144 a0001c0001t0084g0143 |
3 | HG00423.hp2 HG02071.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-136+15684C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877111 | |||||||
chr18:61877201 | G | A | 1 | a0001c0001t0015g0262 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136+15594C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877201 | |||||||
chr18:61877292 | A | G | 2 | a0001c0002t0056g0167 a0001c0002t0057g0168 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-136+15503T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877292 | |||||||
chr18:61877497 | C | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+15298G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877497 | |||||||
chr18:61877602 | T | C | 2 | a0001c0002t0017g0172 a0001c0002t0017g0173 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-136+15193A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877602 | |||||||
chr18:61877646 | G | T | 1 | a0001c0002t0016g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136+15149C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877646 | |||||||
chr18:61877692 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+15103G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877692 | |||||||
chr18:61877757 | C | A | 1 | a0001c0001t0034g0196 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-136+15038G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877757 | |||||||
chr18:61877767 | T | G | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+15028A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877767 | |||||||
chr18:61877968 | C | A | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0006g0269 others(6): Show |
9 | HG01070.hp2 HG01106.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+14827G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877968 | |||||||
chr18:61878068 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(74): Show |
79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+14727G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878068 | |||||||
chr18:61878088 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+14707G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878088 | |||||||
chr18:61878159 | C | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+14636G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878159 | |||||||
chr18:61878312 | A | C | 5 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0011g0197 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+14483T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878312 | |||||||
chr18:61878318 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-136+14477C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878318 | |||||||
chr18:61878471 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0190 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-136+14324G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878471 | |||||||
chr18:61878472 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+14323C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878472 | |||||||
chr18:61878656 | C | T | 2 | a0001c0001t0003g0301 a0001c0001t0003g0302 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-136+14139G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878656 | |||||||
chr18:61878749 | C | T | 1 | a0001c0002t0056g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-136+14046G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878749 | |||||||
chr18:61878818 | C | G | 6 | a0001c0001t0012g0264 a0001c0001t0012g0265 a0001c0001t0020g0284 others(3): Show |
6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+13977G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878818 | |||||||
chr18:61878942 | G | A | 1 | a0001c0002t0016g0018 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-136+13853C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878942 | |||||||
chr18:61879020 | T | G | 19 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+13775A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879020 | |||||||
chr18:61879191 | G | A | 1 | a0001c0002t0005g0216 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-136+13604C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879191 | |||||||
chr18:61879274 | T | G | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+13521A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879274 | |||||||
chr18:61879288 | C | T | 1 | a0001c0002t0005g0022 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136+13507G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879288 | |||||||
chr18:61879295 | AT | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13499delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879295 | |||||||
chr18:61879299 | C | G | 2 | a0001c0001t0042g0280 a0001c0001t0042g0281 |
2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-136+13496G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879299 | |||||||
chr18:61879472 | C | T | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+13323G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879472 | |||||||
chr18:61879473 | G | A | 1 | a0001c0001t0090g0021 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-136+13322C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879473 | |||||||
chr18:61879521 | C | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13274G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879521 | |||||||
chr18:61879561 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13234C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879561 | |||||||
chr18:61879793 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+13002T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879793 | |||||||
chr18:61879833 | C | T | 2 | a0001c0001t0100g0078 a0001c0002t0018g0079 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-136+12962G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879833 | |||||||
chr18:61879837 | C | T | 2 | a0001c0002t0045g0254 a0001c0002t0064g0253 |
2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-136+12958G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879837 | |||||||
chr18:61879842 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-136+12953C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879842 | |||||||
chr18:61879920 | C | G | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+12875G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879920 | |||||||
chr18:61879953 | G | A | 14 | a0001c0001t0002g0201 a0001c0001t0003g0193 a0001c0001t0003g0200 others(11): Show |
14 | HG01346.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136+12842C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879953 | |||||||
chr18:61879965 | CA | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-136+12829delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879965 | |||||||
chr18:61879965 | CAA | C | 11 | a0001c0001t0002g0020 a0001c0001t0007g0077 a0001c0001t0008g0293 others(8): Show |
11 | HG01169.hp2 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-136+12828_-136+12 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879965 | |||||||
chr18:61879982 | T | A | 6 | a0001c0001t0003g0190 a0001c0001t0115g0306 a0001c0001t0117g0305 others(3): Show |
6 | HG02155.hp1 HG02735.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+12813A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879982 | |||||||
chr18:61879992 | G | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-136+12803C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879992 | |||||||
chr18:61880185 | C | T | 7 | a0001c0001t0006g0056 a0001c0002t0005g0016 a0001c0002t0005g0017 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+12610G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880185 | |||||||
chr18:61880279 | T | A | 7 | a0001c0001t0074g0212 a0001c0001t0075g0211 a0001c0001t0091g0213 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+12516A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880279 | |||||||
chr18:61880545 | T | G | 89 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-136+12250A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880545 | |||||||
chr18:61880638 | T | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+12157A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880638 | |||||||
chr18:61880742 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-136+12053C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880742 | |||||||
chr18:61880752 | T | C | 3 | a0001c0001t0115g0306 a0001c0001t0117g0305 a0003c0005t0068g0191 |
3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+12043A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880752 | |||||||
chr18:61880913 | C | CT | 12 | a0001c0001t0003g0145 a0001c0001t0004g0146 a0001c0001t0008g0293 others(9): Show |
12 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+11881dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | |||||||
chr18:61880913 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(97): Show |
102 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-136+11881delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | |||||||
chr18:61880913 | CTT | C | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+11880_-136+11 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | |||||||
chr18:61880935 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-136+11860G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880935 | |||||||
chr18:61881017 | G | A | 3 | a0001c0001t0115g0306 a0001c0001t0117g0305 a0003c0005t0068g0191 |
3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+11778C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881017 | |||||||
chr18:61881020 | TCTC | T | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+11772_-136+11 others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881020 | |||||||
chr18:61881059 | G | A | 1 | a0001c0001t0032g0125 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-136+11736C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881059 | |||||||
chr18:61881113 | C | T | 3 | a0001c0001t0039g0183 a0001c0001t0039g0184 a0001c0001t0103g0068 |
3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+11682G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881113 | |||||||
chr18:61881222 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG03195.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-136+11573G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881222 | |||||||
chr18:61881264 | T | C | 1 | a0001c0001t0101g0174 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+11531A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881264 | |||||||
chr18:61881279 | A | T | 9 | a0001c0001t0001g0075 a0001c0001t0001g0130 a0001c0001t0006g0073 others(6): Show |
9 | HG00738.hp2 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+11516T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881279 | |||||||
chr18:61881567 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+11228G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881567 | |||||||
chr18:61881585 | A | C | 87 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.-136+11210T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881585 | |||||||
chr18:61881592 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+11203C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881592 | |||||||
chr18:61881657 | T | C | 3 | a0001c0001t0115g0306 a0001c0001t0117g0305 a0003c0005t0068g0191 |
3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+11138A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881657 | |||||||
chr18:61881742 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+11053C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881742 | |||||||
chr18:61881752 | G | A | 5 | a0001c0001t0003g0190 a0001c0001t0115g0306 a0001c0001t0117g0305 others(2): Show |
5 | HG02257.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+11043C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881752 | |||||||
chr18:61881881 | T | A | 2 | a0001c0001t0081g0139 a0001c0001t0089g0140 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+10914A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881881 | |||||||
chr18:61881916 | C | A | 1 | a0001c0001t0113g0003 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-136+10879G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881916 | |||||||
chr18:61882046 | G | A | 1 | a0001c0003t0026g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-136+10749C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882046 | |||||||
chr18:61882064 | A | G | 6 | a0001c0001t0074g0212 a0001c0001t0075g0211 a0001c0001t0091g0213 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+10731T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882064 | |||||||
chr18:61882158 | C | T | 4 | a0001c0001t0003g0190 a0001c0001t0115g0306 a0001c0001t0117g0305 others(1): Show |
4 | HG02809.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+10637G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882158 | |||||||
chr18:61882300 | C | A | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+10495G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882300 | |||||||
chr18:61882371 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02155.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-136+10424C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882371 | |||||||
chr18:61882464 | C | T | 1 | a0001c0002t0005g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-136+10331G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882464 | |||||||
chr18:61882678 | G | A | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+10117C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882678 | |||||||
chr18:61882833 | T | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-136+9962A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882833 | |||||||
chr18:61883194 | A | C | 3 | a0001c0001t0003g0142 a0001c0001t0003g0144 a0001c0001t0084g0143 |
3 | HG00423.hp2 HG02071.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-136+9601T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883194 | |||||||
chr18:61883209 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-136+9586T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883209 | |||||||
chr18:61883270 | G | A | 1 | a0001c0002t0005g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-136+9525C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883270 | |||||||
chr18:61883286 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+9509C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883286 | |||||||
chr18:61883384 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0004g0127 a0001c0001t0079g0128 |
3 | NA18947.hp1 NA19060.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-136+9411A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883384 | |||||||
chr18:61883758 | C | T | 3 | a0001c0001t0039g0183 a0001c0001t0039g0184 a0001c0001t0103g0068 |
3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+9037G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883758 | |||||||
chr18:61883861 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+8934A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883861 | |||||||
chr18:61883967 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8828G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883967 | |||||||
chr18:61884053 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-136+8742T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884053 | |||||||
chr18:61884078 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0003g0202 a0001c0001t0004g0203 others(2): Show |
5 | HG01346.hp1 HG02145.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+8717A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884078 | |||||||
chr18:61884228 | G | T | 6 | a0001c0001t0012g0264 a0001c0001t0012g0265 a0001c0001t0020g0284 others(3): Show |
6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+8567C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884228 | |||||||
chr18:61884229 | C | T | 6 | a0001c0001t0012g0264 a0001c0001t0012g0265 a0001c0001t0020g0284 others(3): Show |
6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+8566G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884229 | |||||||
chr18:61884243 | A | AG | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8551_-136+855 others(5): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884243 | |||||||
chr18:61884295 | C | A | 1 | a0001c0002t0055g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-136+8500G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884295 | |||||||
chr18:61884390 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-136+8405C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884390 | |||||||
chr18:61884399 | T | C | 1 | a0001c0001t0027g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-136+8396A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884399 | |||||||
chr18:61884444 | CA | C | 9 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(6): Show |
9 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+8350delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884444 | |||||||
chr18:61884444 | CAA | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(192): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-136+8349_-136+835 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884444 | |||||||
chr18:61884453 | A | T | 9 | a0001c0001t0101g0174 a0001c0002t0017g0169 a0001c0002t0017g0172 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+8342T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884453 | |||||||
chr18:61884637 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8158G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884637 | |||||||
chr18:61884718 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+8077G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884718 | |||||||
chr18:61884722 | C | T | 1 | a0001c0001t0008g0293 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-136+8073G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884722 | |||||||
chr18:61884789 | C | T | 4 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0095g0304 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+8006G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884789 | |||||||
chr18:61884814 | C | T | 1 | a0001c0001t0014g0298 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-136+7981G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884814 | |||||||
chr18:61884906 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+7889A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884906 | |||||||
chr18:61885230 | T | G | 1 | a0001c0008t0004g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-136+7565A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885230 | |||||||
chr18:61885310 | T | TTTTGTTT others(1): Show |
197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+7477_-136+748 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885310 | |||||||
chr18:61885588 | G | A | 1 | a0001c0002t0005g0057 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-136+7207C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885588 | |||||||
chr18:61885601 | C | A | 2 | a0001c0001t0039g0183 a0001c0001t0039g0184 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+7194G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885601 | |||||||
chr18:61885723 | A | G | 1 | a0001c0001t0008g0141 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-136+7072T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885723 | |||||||
chr18:61885770 | G | C | 1 | a0001c0001t0037g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136+7025C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885770 | |||||||
chr18:61885818 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+6977C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885818 | |||||||
chr18:61885856 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0031g0192 |
2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-136+6939G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885856 | |||||||
chr18:61885887 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+6908C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885887 | |||||||
chr18:61885907 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+6888C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885907 | |||||||
chr18:61885975 | CTTTTGCT others(5): Show |
C | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+6808_-136+681 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885975 | |||||||
chr18:61885985 | C | CT | 8 | a0001c0001t0029g0224 a0001c0001t0078g0215 a0001c0001t0108g0242 others(5): Show |
8 | HG01167.hp1 HG01255.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+6809dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CT | C | 21 | a0001c0001t0001g0214 a0001c0001t0001g0220 a0001c0001t0001g0244 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-136+6809delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTT | C | 33 | a0001c0001t0001g0276 a0001c0001t0001g0279 a0001c0001t0002g0201 others(30): Show |
33 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-136+6808_-136+680 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTT | C | 8 | a0001c0001t0003g0200 a0001c0001t0003g0301 a0001c0001t0003g0302 others(5): Show |
8 | HG01192.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+6807_-136+680 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTTTTTT | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0091 a0001c0001t0001g0119 others(14): Show |
17 | HG00323.hp1 HG00597.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+6803_-136+680 others(11): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTTTTTT others(1): Show |
C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-136+6802_-136+680 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0003g0190 others(16): Show |
19 | HG01192.hp2 HG02258.hp2 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+6801_-136+680 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0098g0179 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-136+6800_-136+680 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61885985 | CTTTTTTT others(4): Show |
C | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+6799_-136+680 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | |||||||
chr18:61886127 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+6668A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886127 | |||||||
chr18:61886201 | T | G | 22 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(19): Show |
22 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136+6594A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886201 | |||||||
chr18:61886296 | T | C | 1 | a0001c0004t0094g0252 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-136+6499A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886296 | |||||||
chr18:61886561 | T | C | 1 | a0001c0002t0066g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136+6234A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886561 | |||||||
chr18:61886641 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+6154T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886641 | |||||||
chr18:61886688 | C | G | 1 | a0001c0002t0048g0292 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-136+6107G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886688 | |||||||
chr18:61886789 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(74): Show |
79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+6006C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886789 | |||||||
chr18:61886800 | C | T | 2 | a0001c0001t0081g0139 a0001c0001t0089g0140 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+5995G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886800 | |||||||
chr18:61886996 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-136+5799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886996 | |||||||
chr18:61887040 | A | G | 5 | a0001c0001t0003g0193 a0001c0001t0003g0200 a0001c0001t0011g0197 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+5755T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887040 | |||||||
chr18:61887131 | G | A | 1 | a0003c0005t0068g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+5664C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887131 | |||||||
chr18:61887408 | GA | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+5386delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887408 | |||||||
chr18:61887414 | G | A | 2 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
2 | HG00280.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-136+5381C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887414 | |||||||
chr18:61887432 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-136+5363G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887432 | |||||||
chr18:61887651 | G | T | 13 | a0001c0001t0037g0182 a0001c0001t0038g0136 a0001c0001t0038g0137 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+5144C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887651 | |||||||
chr18:61887688 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(244): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-136+5107A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887688 | |||||||
chr18:61887701 | C | CA | 14 | a0001c0001t0003g0302 a0001c0001t0006g0286 a0001c0001t0020g0284 others(11): Show |
14 | HG01175.hp1 HG01433.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+5093dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | |||||||
chr18:61887701 | CA | C | 112 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-136+5093delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | |||||||
chr18:61887701 | CAA | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(75): Show |
80 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-136+5092_-136+509 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | |||||||
chr18:61887832 | C | A | 2 | a0001c0001t0015g0258 a0001c0002t0063g0257 |
2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+4963G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887832 | |||||||
chr18:61887854 | C | T | 1 | a0001c0001t0004g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-136+4941G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887854 | |||||||
chr18:61888104 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+4691A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888104 | |||||||
chr18:61888172 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+4623C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888172 | |||||||
chr18:61888204 | G | A | 2 | a0001c0001t0020g0288 a0001c0001t0083g0287 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-136+4591C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888204 | |||||||
chr18:61888239 | C | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(73): Show |
78 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-136+4556G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888239 | |||||||
chr18:61888323 | T | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-136+4472A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888323 | |||||||
chr18:61888423 | T | C | 2 | a0001c0001t0039g0183 a0001c0001t0039g0184 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+4372A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888423 | |||||||
chr18:61888525 | A | C | 3 | a0001c0001t0015g0261 a0001c0001t0015g0262 a0001c0001t0119g0260 |
3 | HG01109.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-136+4270T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888525 | |||||||
chr18:61888764 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0031g0192 |
2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-136+4031C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888764 | |||||||
chr18:61888831 | C | T | 1 | a0001c0002t0009g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-136+3964G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888831 | |||||||
chr18:61888840 | T | C | 3 | a0001c0002t0018g0186 a0001c0002t0018g0300 a0001c0002t0066g0187 |
3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-136+3955A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888840 | |||||||
chr18:61889096 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-136+3699A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889096 | |||||||
chr18:61889141 | G | T | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+3654C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889141 | |||||||
chr18:61889188 | A | G | 1 | a0001c0001t0011g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-136+3607T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889188 | |||||||
chr18:61889464 | C | T | 1 | a0001c0001t0006g0065 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-136+3331G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889464 | |||||||
chr18:61889484 | G | C | 1 | a0001c0002t0069g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-136+3311C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889484 | |||||||
chr18:61889563 | C | T | 2 | a0001c0001t0006g0063 a0001c0008t0004g0064 |
2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-136+3232G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889563 | |||||||
chr18:61889718 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0006g0062 |
2 | NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-136+3077G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889718 | |||||||
chr18:61889723 | C | G | 1 | a0001c0001t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+3072G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889723 | |||||||
chr18:61889879 | T | A | 5 | a0001c0001t0003g0190 a0001c0001t0115g0306 a0001c0001t0117g0305 others(2): Show |
5 | HG02257.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+2916A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889879 | |||||||
chr18:61889958 | C | T | 1 | a0001c0001t0022g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-136+2837G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889958 | |||||||
chr18:61890048 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+2747G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890048 | |||||||
chr18:61890218 | C | G | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+2577G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890218 | |||||||
chr18:61890267 | T | C | 1 | a0001c0001t0031g0192 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-136+2528A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890267 | |||||||
chr18:61890395 | A | C | 56 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0047 others(53): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-136+2400T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890395 | |||||||
chr18:61890404 | C | A | 2 | a0001c0001t0015g0258 a0001c0002t0063g0257 |
2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+2391G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890404 | |||||||
chr18:61890537 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+2258T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890537 | |||||||
chr18:61890690 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+2105T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890690 | |||||||
chr18:61890764 | T | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+2031A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890764 | |||||||
chr18:61890819 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(187): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-136+1976A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890819 | |||||||
chr18:61890827 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+1968G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890827 | |||||||
chr18:61890851 | A | G | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+1944T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890851 | |||||||
chr18:61891019 | G | C | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+1776C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891019 | |||||||
chr18:61891435 | TA | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+1359delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891435 | |||||||
chr18:61891835 | A | C | 41 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(38): Show |
41 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.-136+960T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891835 | |||||||
chr18:61891863 | G | C | 29 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0279 others(26): Show |
29 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.-136+932C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891863 | |||||||
chr18:61891912 | G | A | 7 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0001t0080g0194 others(4): Show |
7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+883C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891912 | |||||||
chr18:61891927 | T | C | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0082g0291 |
3 | HG02129.hp2 HG02155.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-136+868A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891927 | |||||||
chr18:61891982 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+813G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891982 | |||||||
chr18:61892014 | G | A | 5 | a0001c0001t0008g0293 a0001c0001t0076g0294 a0001c0002t0048g0292 others(2): Show |
5 | HG01258.hp2 HG01934.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+781C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892014 | |||||||
chr18:61892071 | G | A | 1 | a0001c0002t0058g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+724C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892071 | |||||||
chr18:61892274 | C | T | 1 | a0001c0001t0006g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-136+521G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892274 | |||||||
chr18:61892383 | G | A | 2 | a0001c0001t0014g0298 a0001c0001t0028g0299 |
2 | NA18943.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-136+412C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892383 | |||||||
chr18:61892457 | T | C | 1 | a0001c0002t0018g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-136+338A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892457 | |||||||
chr18:61892498 | AAC | A | 4 | a0001c0001t0003g0301 a0001c0001t0003g0302 a0001c0001t0095g0304 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+295_-136+296d others(4): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892498 | |||||||
chr18:61892658 | G | A | 2 | a0001c0001t0115g0306 a0001c0001t0117g0305 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+137C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892658 | |||||||
chr18:61892739 | T | C | 2 | a0001c0002t0009g0307 a0001c0002t0009g0308 |
2 | HG00423.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-136+56A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892739 | |||||||
chr18:61892794 | C | T | 1 | a0001c0001t0113g0003 | 1 | HG01099.hp2 | splice_donor_variant&intron_variant | HIGH | c.-136+1G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892794 |