Item | Value |
---|---|
geneid | 150864 |
ensemblid | ENSG00000138439.12 |
hgncid | 14440 |
symbol | FAM117B |
name | family with sequence similarity 117 member B |
refseq_nuc | NM_173511.4 |
refseq_prot | NP_775782.2 |
ensembl_nuc | ENST00000392238.3 |
ensembl_prot | ENSP00000376071.2 |
mane_status | MANE Select |
chr | chr2 |
start | 202634969 |
end | 202769757 |
strand | + |
ver | v1.2 |
region | chr2:202634969-202769757 |
region5000 | chr2:202629969-202774757 |
regionname0 | FAM117B_chr2_202634969_202769757 |
regionname5000 | FAM117B_chr2_202629969_202774757 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 589 | 279 | 48 | 59 | 124 | 6 | 40 | 90 | FAM117B_chr2_202629969_202774757 | FAM117B | MSQRV others(584): Show |
chr2 | 202629969 | 202774757 |
a0002 | 0/0 | 590 | 30 | 25 | 5 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | MSQRV others(585): Show |
chr2 | 202629969 | 202774757 |
a0003 | 0/0 | 591 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | MSQRV others(586): Show |
chr2 | 202629969 | 202774757 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1767 | 272 | 46 | 55 | 123 | 6 | 40 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1762): Show |
chr2 | 202629969 | 202774757 | ||
a0001c0004 | 0/0 | 1767 | 4 | 0 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1762): Show |
chr2 | 202629969 | 202774757 | ||
a0001c0006 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1762): Show |
chr2 | 202629969 | 202774757 | ||
a0001c0007 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1762): Show |
chr2 | 202629969 | 202774757 | ||
a0001c0008 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1762): Show |
chr2 | 202629969 | 202774757 | ||
a0002c0002 | 0/0 | 1770 | 29 | 24 | 5 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1765): Show |
chr2 | 202629969 | 202774757 | ||
a0002c0005 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1765): Show |
chr2 | 202629969 | 202774757 | ||
a0003c0003 | 0/0 | 1773 | 9 | 9 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | ATGTC others(1768): Show |
chr2 | 202629969 | 202774757 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5982 | 37 | 2 | 9 | 19 | 1 | 6 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0002 | 0/0 | 5981 | 21 | 0 | 3 | 16 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0003 | 0/0 | 5984 | 12 | 1 | 3 | 8 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0004 | 0/0 | 5974 | 12 | 1 | 5 | 4 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5969): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0005 | 1/0 | 5982 | 11 | 2 | 1 | 4 | 0 | 3 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0007 | 0/0 | 5983 | 7 | 0 | 3 | 2 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0008 | 0/0 | 5980 | 7 | 3 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0009 | 0/0 | 5980 | 7 | 1 | 1 | 3 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0010 | 0/0 | 5981 | 5 | 3 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0011 | 0/0 | 5979 | 5 | 0 | 3 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5974): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0013 | 0/0 | 5978 | 5 | 0 | 1 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0014 | 0/0 | 5983 | 5 | 0 | 0 | 3 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0015 | 0/0 | 5984 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0017 | 0/0 | 5984 | 4 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0018 | 0/0 | 5961 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5956): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0019 | 0/0 | 5978 | 4 | 0 | 2 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0020 | 0/0 | 5974 | 4 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5969): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0022 | 0/0 | 5998 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5993): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0023 | 0/0 | 5991 | 3 | 1 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5986): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0024 | 0/0 | 5990 | 3 | 0 | 1 | 1 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5985): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0025 | 0/0 | 5980 | 3 | 1 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0026 | 0/0 | 5981 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0027 | 0/0 | 5982 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0028 | 0/0 | 5978 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0029 | 0/0 | 5972 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0030 | 0/0 | 5973 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5968): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0031 | 0/0 | 5976 | 3 | 0 | 0 | 2 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5971): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0032 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0033 | 0/0 | 5988 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5983): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0034 | 0/0 | 5985 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0035 | 0/0 | 5983 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0036 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5972): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0039 | 0/0 | 5989 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5984): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0040 | 0/0 | 5985 | 2 | 0 | 1 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0041 | 0/0 | 5988 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5983): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0042 | 0/0 | 5981 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0043 | 0/0 | 5983 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0044 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0045 | 0/0 | 5985 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0046 | 0/0 | 5983 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0047 | 0/0 | 5978 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0048 | 0/0 | 5978 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0049 | 0/0 | 5976 | 2 | 0 | 1 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5971): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0050 | 0/0 | 5974 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5969): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0051 | 0/0 | 5980 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0052 | 0/0 | 5998 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5993): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0053 | 0/0 | 5996 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5991): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0054 | 0/0 | 5992 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5987): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0055 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0056 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0057 | 0/0 | 5986 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5981): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0063 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5972): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0064 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0065 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5974): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0072 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5969): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0077 | 0/0 | 5992 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5987): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0078 | 0/0 | 5993 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5988): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0079 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5989): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0080 | 0/0 | 5992 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5987): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0081 | 0/0 | 5985 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0082 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5981): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0083 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0084 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5981): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0085 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5982): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0086 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0087 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0088 | 0/0 | 5982 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0089 | 0/0 | 5981 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0090 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0091 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0092 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0093 | 0/0 | 5984 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0094 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0095 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0096 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0097 | 0/0 | 5982 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0098 | 0/0 | 5982 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0099 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0100 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0101 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5970): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0102 | 0/0 | 5973 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5968): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0103 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0104 | 0/0 | 5966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5961): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0105 | 0/0 | 5963 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5958): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0106 | 0/0 | 5960 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5955): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0107 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5985): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0108 | 0/0 | 6001 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5996): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0109 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0111 | 0/0 | 5985 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5980): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0113 | 0/0 | 5976 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5971): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0114 | 0/0 | 5984 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0115 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5982): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0116 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0117 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5974): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0118 | 0/0 | 5976 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5971): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0119 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5969): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0120 | 0/1 | 5978 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0121 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0001t0122 | 0/0 | 5975 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5970): Show |
chr2 | 202629969 | 202774757 |
a0001c0004t0038 | 0/0 | 5995 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5990): Show |
chr2 | 202629969 | 202774757 |
a0001c0004t0075 | 0/0 | 5999 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5994): Show |
chr2 | 202629969 | 202774757 |
a0001c0004t0076 | 0/0 | 5997 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5992): Show |
chr2 | 202629969 | 202774757 |
a0001c0006t0110 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5979): Show |
chr2 | 202629969 | 202774757 |
a0001c0007t0068 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5964): Show |
chr2 | 202629969 | 202774757 |
a0001c0008t0074 | 0/0 | 5998 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5993): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0006 | 0/0 | 5972 | 9 | 5 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0016 | 0/0 | 5982 | 3 | 2 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0021 | 0/0 | 5976 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5971): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0032 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5970): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0037 | 0/0 | 5958 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5953): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0058 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5970): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0059 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0060 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0061 | 0/0 | 5981 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5976): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0062 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5975): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0066 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5972): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0067 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0069 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5967): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0070 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0071 | 0/0 | 6335 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(6330): Show |
chr2 | 202629969 | 202774757 |
a0002c0002t0073 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5972): Show |
chr2 | 202629969 | 202774757 |
a0002c0005t0016 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0003c0003t0010 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5982): Show |
chr2 | 202629969 | 202774757 |
a0003c0003t0012 | 0/0 | 5982 | 5 | 5 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5977): Show |
chr2 | 202629969 | 202774757 |
a0003c0003t0032 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5973): Show |
chr2 | 202629969 | 202774757 |
a0003c0003t0044 | 0/0 | 5986 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5981): Show |
chr2 | 202629969 | 202774757 |
a0003c0003t0112 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | AGAGG others(5978): Show |
chr2 | 202629969 | 202774757 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0010g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0010g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0024g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0030g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0030g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0032g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0033g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0033g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0034g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0035g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0035g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0036g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0036g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0039g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0039g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0040g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0040g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0041g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0041g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0042g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0042g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0043g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0043g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0044g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0045g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0045g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0046g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0046g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0047g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0047g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0048g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0048g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0049g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0049g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0050g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0050g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0051g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0051g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0052g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0053g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0054g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0055g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0056g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0057g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0063g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0064g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0065g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0072g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0077g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0078g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0079g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0080g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0081g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0082g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0083g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0084g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0085g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0086g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0087g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0088g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0089g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0090g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0091g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0092g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0093g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0094g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0095g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0096g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0097g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0098g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0099g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0100g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0101g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0102g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0103g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0104g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0105g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0106g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0107g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0108g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0109g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0111g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0113g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0114g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0115g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0116g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0117g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0118g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0119g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0120g0001 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0121g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0122g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0038g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0038g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0075g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0076g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0006t0110g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0007t0068g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0008t0074g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0006g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0021g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0021g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0021g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0032g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0037g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0037g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0058g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0059g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0060g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0061g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0062g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0066g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0067g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0069g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0070g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0071g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0073g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0005t0016g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0012g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0032g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0044g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0112g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0039 | g0015 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00099 | hp2 | a0001 | c0001 | t0024 | g0177 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00140 | hp1 | a0001 | c0001 | t0051 | g0179 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00140 | hp2 | a0001 | c0001 | t0019 | g0034 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00323 | hp2 | a0001 | c0001 | t0042 | g0264 | EUR | FIN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00408 | hp1 | a0001 | c0001 | t0077 | g0210 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00544 | hp1 | a0001 | c0001 | t0092 | g0211 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00544 | hp2 | a0001 | c0001 | t0122 | g0009 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00558 | hp2 | a0001 | c0001 | t0015 | g0279 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00597 | hp1 | a0001 | c0001 | t0084 | g0134 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00597 | hp2 | a0001 | c0001 | t0035 | g0278 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00609 | hp1 | a0001 | c0001 | t0121 | g0047 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00609 | hp2 | a0001 | c0001 | t0013 | g0041 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00639 | hp2 | a0001 | c0001 | t0113 | g0263 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00642 | hp1 | a0001 | c0001 | t0119 | g0023 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0094 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00733 | hp1 | a0002 | c0002 | t0006 | g0314 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00733 | hp2 | a0001 | c0001 | t0086 | g0265 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00738 | hp2 | a0001 | c0001 | t0017 | g0050 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00741 | hp2 | a0001 | c0001 | t0020 | g0032 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01081 | hp2 | a0001 | c0001 | t0017 | g0040 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01099 | hp2 | a0001 | c0001 | t0109 | g0258 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0030 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01106 | hp2 | a0001 | c0004 | t0076 | g0056 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0078 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01109 | hp2 | a0002 | c0002 | t0006 | g0302 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01167 | hp1 | a0001 | c0001 | t0019 | g0035 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01167 | hp2 | a0001 | c0004 | t0038 | g0012 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01168 | hp1 | a0002 | c0002 | t0006 | g0312 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01169 | hp1 | a0002 | c0002 | t0006 | g0313 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01169 | hp2 | a0001 | c0004 | t0038 | g0013 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0100 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0137 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01243 | hp1 | a0002 | c0002 | t0016 | g0296 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0165 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01255 | hp1 | a0001 | c0001 | t0099 | g0175 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0189 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01261 | hp1 | a0001 | c0001 | t0025 | g0259 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01261 | hp2 | a0001 | c0001 | t0072 | g0025 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01346 | hp1 | a0001 | c0001 | t0051 | g0111 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01346 | hp2 | a0001 | c0001 | t0090 | g0260 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01358 | hp1 | a0001 | c0001 | t0096 | g0148 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01358 | hp2 | a0001 | c0004 | t0075 | g0055 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01361 | hp1 | a0001 | c0001 | t0007 | g0076 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01433 | hp1 | a0001 | c0001 | t0019 | g0033 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0067 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01496 | hp1 | a0001 | c0001 | t0025 | g0213 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01884 | hp1 | a0001 | c0001 | t0107 | g0266 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01884 | hp2 | a0002 | c0002 | t0021 | g0289 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01891 | hp1 | a0001 | c0001 | t0050 | g0270 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01891 | hp2 | a0001 | c0001 | t0023 | g0086 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0049 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01943 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01952 | hp2 | a0001 | c0001 | t0047 | g0225 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0122 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01981 | hp1 | a0001 | c0001 | t0108 | g0180 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02055 | hp2 | a0001 | c0001 | t0044 | g0267 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02071 | hp1 | a0001 | c0001 | t0013 | g0132 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02080 | hp1 | a0001 | c0001 | t0055 | g0282 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02080 | hp2 | a0001 | c0001 | t0085 | g0052 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02083 | hp1 | a0001 | c0001 | t0033 | g0281 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02083 | hp2 | a0001 | c0001 | t0022 | g0201 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02132 | hp1 | a0001 | c0001 | t0115 | g0048 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02132 | hp2 | a0001 | c0001 | t0027 | g0235 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02145 | hp1 | a0003 | c0003 | t0112 | g0249 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02145 | hp2 | a0001 | c0001 | t0057 | g0205 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02155 | hp1 | a0001 | c0001 | t0022 | g0110 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02165 | hp1 | a0001 | c0001 | t0041 | g0138 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02257 | hp1 | a0001 | c0001 | t0034 | g0185 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02258 | hp1 | a0002 | c0002 | t0061 | g0310 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02258 | hp2 | a0001 | c0001 | t0026 | g0252 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02273 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02293 | hp1 | a0001 | c0001 | t0024 | g0222 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02293 | hp2 | a0001 | c0001 | t0049 | g0223 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02300 | hp1 | a0001 | c0001 | t0007 | g0066 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02300 | hp2 | a0001 | c0001 | t0040 | g0208 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02451 | hp1 | a0003 | c0003 | t0012 | g0246 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02451 | hp2 | a0002 | c0002 | t0067 | g0315 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02523 | hp1 | a0001 | c0001 | t0091 | g0188 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02523 | hp2 | a0001 | c0001 | t0023 | g0159 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02572 | hp1 | a0002 | c0002 | t0006 | g0305 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0104 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02602 | hp2 | a0001 | c0001 | t0111 | g0244 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0224 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02615 | hp2 | a0002 | c0002 | t0071 | g0301 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02622 | hp1 | a0001 | c0001 | t0035 | g0183 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02683 | hp2 | a0001 | c0001 | t0081 | g0087 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02698 | hp2 | a0001 | c0001 | t0042 | g0257 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02717 | hp1 | a0002 | c0002 | t0006 | g0308 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02717 | hp2 | a0003 | c0003 | t0012 | g0247 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02723 | hp1 | a0002 | c0002 | t0016 | g0299 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02723 | hp2 | a0001 | c0001 | t0064 | g0284 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02738 | hp1 | a0001 | c0001 | t0019 | g0036 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02818 | hp1 | a0002 | c0002 | t0069 | g0303 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02818 | hp2 | a0001 | c0001 | t0030 | g0127 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02886 | hp1 | a0002 | c0002 | t0062 | g0304 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02886 | hp2 | a0003 | c0003 | t0010 | g0103 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02895 | hp1 | a0002 | c0002 | t0037 | g0293 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02895 | hp2 | a0003 | c0003 | t0044 | g0063 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02896 | hp1 | a0002 | c0002 | t0006 | g0306 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02896 | hp2 | a0003 | c0003 | t0012 | g0248 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02897 | hp1 | a0002 | c0002 | t0037 | g0311 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02897 | hp2 | a0003 | c0003 | t0012 | g0062 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02965 | hp1 | a0001 | c0001 | t0028 | g0162 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0254 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02970 | hp1 | a0002 | c0005 | t0016 | g0298 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02970 | hp2 | a0001 | c0008 | t0074 | g0116 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02976 | hp1 | a0001 | c0001 | t0101 | g0174 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0214 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03017 | hp2 | a0001 | c0001 | t0009 | g0084 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03041 | hp1 | a0002 | c0002 | t0032 | g0294 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03041 | hp2 | a0001 | c0001 | t0030 | g0005 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03098 | hp1 | a0001 | c0001 | t0032 | g0007 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03098 | hp2 | a0002 | c0002 | t0060 | g0317 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03130 | hp1 | a0001 | c0001 | t0095 | g0199 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03130 | hp2 | a0002 | c0002 | t0021 | g0290 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03139 | hp1 | a0001 | c0001 | t0047 | g0006 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03139 | hp2 | a0001 | c0001 | t0036 | g0286 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03195 | hp1 | a0001 | c0001 | t0029 | g0269 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03195 | hp2 | a0001 | c0001 | t0100 | g0204 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03209 | hp1 | a0002 | c0002 | t0070 | g0295 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03209 | hp2 | a0001 | c0001 | t0103 | g0109 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03225 | hp1 | a0001 | c0001 | t0083 | g0102 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03225 | hp2 | a0002 | c0002 | t0058 | g0318 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03453 | hp1 | a0001 | c0007 | t0068 | g0285 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03490 | hp2 | a0001 | c0001 | t0102 | g0262 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03491 | hp2 | a0001 | c0001 | t0020 | g0021 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03492 | hp2 | a0001 | c0001 | t0020 | g0024 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03516 | hp1 | a0003 | c0003 | t0032 | g0245 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03516 | hp2 | a0002 | c0002 | t0073 | g0292 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03579 | hp1 | a0003 | c0003 | t0012 | g0250 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0161 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03654 | hp1 | a0001 | c0001 | t0014 | g0143 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03669 | hp1 | a0001 | c0001 | t0031 | g0083 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03669 | hp2 | a0001 | c0001 | t0008 | g0226 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03688 | hp2 | a0001 | c0001 | t0080 | g0150 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0221 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03704 | hp2 | a0001 | c0001 | t0089 | g0016 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0238 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03710 | hp2 | a0001 | c0001 | t0014 | g0059 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03831 | hp1 | a0001 | c0001 | t0049 | g0209 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0169 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03927 | hp1 | a0001 | c0001 | t0114 | g0237 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0072 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03942 | hp2 | a0001 | c0001 | t0017 | g0187 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04115 | hp2 | a0001 | c0001 | t0088 | g0198 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04199 | hp1 | a0001 | c0001 | t0045 | g0112 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04199 | hp2 | a0001 | c0001 | t0039 | g0239 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0206 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04204 | hp2 | a0001 | c0001 | t0046 | g0168 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04228 | hp1 | a0001 | c0001 | t0017 | g0197 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04228 | hp2 | a0001 | c0001 | t0093 | g0125 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18522 | hp1 | a0001 | c0001 | t0028 | g0002 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18747 | hp1 | a0001 | c0001 | t0043 | g0099 | EAS | CHB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18747 | hp2 | a0001 | c0001 | t0022 | g0194 | EAS | CHB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18906 | hp1 | a0002 | c0002 | t0016 | g0297 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18906 | hp2 | a0001 | c0001 | t0026 | g0124 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18939 | hp2 | a0001 | c0001 | t0015 | g0271 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18940 | hp1 | a0001 | c0001 | t0046 | g0121 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18940 | hp2 | a0001 | c0001 | t0011 | g0095 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18945 | hp1 | a0001 | c0001 | t0011 | g0283 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18949 | hp1 | a0001 | c0006 | t0110 | g0064 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18950 | hp1 | a0001 | c0001 | t0031 | g0151 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18950 | hp2 | a0001 | c0001 | t0087 | g0190 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18951 | hp1 | a0001 | c0001 | t0023 | g0135 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18952 | hp2 | a0001 | c0001 | t0009 | g0119 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18954 | hp2 | a0001 | c0001 | t0043 | g0069 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18962 | hp2 | a0001 | c0001 | t0024 | g0202 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18964 | hp1 | a0001 | c0001 | t0014 | g0108 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18965 | hp1 | a0001 | c0001 | t0078 | g0096 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18969 | hp1 | a0001 | c0001 | t0104 | g0236 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18969 | hp2 | a0001 | c0001 | t0098 | g0044 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18970 | hp1 | a0001 | c0001 | t0048 | g0129 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18970 | hp2 | a0001 | c0001 | t0117 | g0046 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18972 | hp1 | a0001 | c0001 | t0027 | g0233 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18972 | hp2 | a0001 | c0001 | t0013 | g0170 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18974 | hp1 | a0001 | c0001 | t0053 | g0273 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18974 | hp2 | a0001 | c0001 | t0097 | g0039 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18980 | hp1 | a0001 | c0001 | t0018 | g0182 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18981 | hp1 | a0001 | c0001 | t0079 | g0240 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18981 | hp2 | a0001 | c0001 | t0056 | g0280 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18983 | hp1 | a0001 | c0001 | t0015 | g0275 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18986 | hp2 | a0001 | c0001 | t0116 | g0229 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18988 | hp1 | a0001 | c0001 | t0082 | g0231 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18991 | hp1 | a0001 | c0001 | t0007 | g0082 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18991 | hp2 | a0001 | c0001 | t0045 | g0171 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18994 | hp1 | a0001 | c0001 | t0094 | g0230 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18999 | hp1 | a0001 | c0001 | t0018 | g0181 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19003 | hp1 | a0001 | c0001 | t0054 | g0272 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19004 | hp1 | a0001 | c0001 | t0052 | g0274 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19004 | hp2 | a0001 | c0001 | t0065 | g0126 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19009 | hp1 | a0001 | c0001 | t0105 | g0243 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19009 | hp2 | a0001 | c0001 | t0048 | g0130 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19010 | hp2 | a0001 | c0001 | t0018 | g0192 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19011 | hp1 | a0001 | c0001 | t0041 | g0193 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19030 | hp1 | a0002 | c0002 | t0066 | g0300 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19030 | hp2 | a0002 | c0002 | t0006 | g0309 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19043 | hp1 | a0001 | c0001 | t0034 | g0184 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19043 | hp2 | a0001 | c0001 | t0029 | g0268 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19058 | hp2 | a0001 | c0001 | t0031 | g0157 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19064 | hp1 | a0001 | c0001 | t0027 | g0242 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19064 | hp2 | a0001 | c0001 | t0014 | g0131 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19065 | hp1 | a0001 | c0001 | t0040 | g0195 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19078 | hp1 | a0001 | c0001 | t0014 | g0219 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19078 | hp2 | a0001 | c0001 | t0106 | g0212 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19082 | hp1 | a0001 | c0001 | t0033 | g0277 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19082 | hp2 | a0001 | c0001 | t0118 | g0145 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19083 | hp1 | a0001 | c0001 | t0015 | g0276 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19085 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19088 | hp1 | a0001 | c0001 | t0018 | g0232 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19240 | hp1 | a0001 | c0001 | t0050 | g0053 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0256 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01123 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02109 | hp1 | a0001 | c0001 | t0063 | g0288 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02559 | hp1 | a0001 | c0001 | t0029 | g0079 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02559 | hp2 | a0002 | c0002 | t0006 | g0307 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03471 | hp1 | a0002 | c0002 | t0059 | g0316 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03471 | hp2 | a0001 | c0001 | t0026 | g0251 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG06807 | hp1 | a0001 | c0001 | t0030 | g0128 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG06807 | hp2 | a0002 | c0002 | t0021 | g0291 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA20300 | hp1 | a0001 | c0001 | t0036 | g0287 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA21309 | hp1 | a0001 | c0001 | t0025 | g0261 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0227 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
homoSapiens | chm13v2 | a0001 | c0001 | t0120 | g0001 | REF | REF | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0178 | REF | REF | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635418 | A | AGGC | 1 | a0002 | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
disruptive_inframe_insertion | MODERATE | c.246_248dupCGG | p.Gly83dup | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 468/5982 | 249/1770 | 83/589 | INFO_REALIGN_3_PRIME | chr2 | 202635418 | ||
chr2:202635418 | A | AGGCGGC | 1 | a0003 | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.243_248dupCGGCGG | p.Gly82_Gly83dup | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 468/5982 | 249/1770 | 83/589 | INFO_REALIGN_3_PRIME | chr2 | 202635418 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635226 | G | A | 1 | a0001c0004 | 4 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
synonymous_variant | LOW | c.39G>A | p.Pro13Pro | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 258/5982 | 39/1770 | 13/589 | chr2 | 202635226 | |||
chr2:202695900 | T | C | 1 | a0001c0006 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.621T>C | p.Pro207Pro | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/8 | 840/5982 | 621/1770 | 207/589 | chr2 | 202695900 | |||
chr2:202757305 | G | A | 1 | a0001c0007 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1197G>A | p.Gly399Gly | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/8 | 1416/5982 | 1197/1770 | 399/589 | chr2 | 202757305 | |||
chr2:202757383 | T | C | 1 | a0002c0005 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1275T>C | p.Gly425Gly | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/8 | 1494/5982 | 1275/1770 | 425/589 | chr2 | 202757383 | |||
chr2:202759294 | T | C | 1 | a0001c0008 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1392T>C | p.Tyr464Tyr | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/8 | 1611/5982 | 1392/1770 | 464/589 | chr2 | 202759294 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202634993 | G | GAGC | 10 | a0001c0001t0015 a0001c0001t0033 a0001c0001t0034 others(7): Show |
16 | HG00558.hp2 HG00597.hp2 HG02080.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-194_-192dupAGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 191 | INFO_REALIGN_3_PRIME | chr2 | 202634993 | |||||
chr2:202634994 | AGCG | A | 19 | a0001c0001t0036 a0001c0001t0063 a0001c0001t0064 others(16): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171delGGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 171 | INFO_REALIGN_3_PRIME | chr2 | 202634994 | |||||
chr2:202634994 | AGCGGCG | A | 11 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(8): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-171delGGCGGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 171 | INFO_REALIGN_3_PRIME | chr2 | 202634994 | |||||
chr2:202634997 | G | A | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-191G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 191 | chr2 | 202634997 | ||||||
chr2:202635000 | G | A | 19 | a0001c0001t0036 a0001c0001t0063 a0001c0001t0064 others(16): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 188 | chr2 | 202635000 | ||||||
chr2:202635003 | G | A | 1 | a0001c0001t0072 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 185 | chr2 | 202635003 | ||||||
chr2:202635108 | C | T | 1 | a0001c0001t0114 | 1 | HG03927.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | chr2 | 202635108 | |||||||
chr2:202635123 | T | TC | 3 | a0002c0002t0021 a0002c0002t0058 a0002c0002t0073 |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-60dupC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr2 | 202635123 | |||||
chr2:202635160 | C | A | 2 | a0002c0002t0059 a0002c0002t0060 |
2 | HG03098.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-28C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 28 | chr2 | 202635160 | ||||||
chr2:202635176 | A | AG | 14 | a0001c0001t0014 a0001c0001t0056 a0001c0001t0057 others(11): Show |
18 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-4dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 3 | INFO_REALIGN_3_PRIME | chr2 | 202635176 | |||||
chr2:202765839 | C | T | 2 | a0001c0001t0020 a0001c0001t0051 |
6 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 75 | chr2 | 202765839 | ||||||
chr2:202765975 | A | G | 1 | a0001c0001t0107 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 211 | chr2 | 202765975 | ||||||
chr2:202766025 | A | G | 1 | a0001c0001t0119 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 261 | chr2 | 202766025 | ||||||
chr2:202766061 | A | AAC | 6 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0083 others(3): Show |
15 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*342_*343dupAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACAC | 6 | a0001c0001t0033 a0001c0001t0040 a0001c0001t0041 others(3): Show |
9 | HG02083.hp1 HG02165.hp1 HG02300.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*343dupACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(1): Show |
6 | a0001c0001t0024 a0001c0001t0039 a0001c0001t0054 others(3): Show |
9 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*336_*343dupACACAC others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(3): Show |
6 | a0001c0001t0023 a0001c0001t0077 a0001c0001t0078 others(3): Show |
8 | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*334_*343dupACACAC others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(5): Show |
1 | a0001c0001t0053 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332_*343dupACACAC others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(7): Show |
2 | a0001c0001t0052 a0001c0004t0038 |
3 | HG01167.hp2 HG01169.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*343dupACACAC others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(9): Show |
2 | a0001c0001t0022 a0001c0004t0076 |
4 | HG01106.hp2 HG02083.hp2 HG02155.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*343dupACACAC others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | A | AACACACA others(11): Show |
3 | a0001c0001t0108 a0001c0004t0075 a0001c0008t0074 |
3 | HG01358.hp2 HG01981.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326_*343dupACACAC others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AAC | A | 18 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(15): Show |
74 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*342_*343delAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 342 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACAC | A | 6 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0047 others(3): Show |
19 | HG00558.hp1 HG01243.hp2 HG01952.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*343delACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 340 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACAC | A | 7 | a0001c0001t0013 a0001c0001t0048 a0001c0001t0049 others(4): Show |
13 | HG00609.hp2 HG00639.hp2 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*338_*343delACACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 338 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(1): Show |
A | 10 | a0001c0001t0029 a0001c0001t0030 a0001c0001t0031 others(7): Show |
18 | HG01884.hp2 HG02451.hp2 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*336_*343delACACAC others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 336 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(3): Show |
A | 5 | a0001c0001t0032 a0001c0001t0050 a0002c0002t0006 others(2): Show |
14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*334_*343delACACAC others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 334 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(5): Show |
A | 1 | a0001c0001t0055 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332_*343delACACAC others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 332 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(9): Show |
A | 1 | a0001c0001t0104 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328_*343delACACAC others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 328 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(11): Show |
A | 1 | a0001c0001t0105 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326_*343delACACAC others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 326 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(13): Show |
A | 2 | a0001c0001t0018 a0001c0001t0106 |
5 | NA18980.hp1 NA18999.hp1 NA19010.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*324_*343delACACAC others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 324 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766061 | AACACACA others(17): Show |
A | 1 | a0002c0002t0037 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320_*343delACACAC others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 320 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | |||||
chr2:202766102 | A | ACACACC | 4 | a0001c0001t0004 a0001c0001t0072 a0001c0001t0119 others(1): Show |
7 | HG00544.hp2 HG00642.hp1 HG01192.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*345dupACACCC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 346 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | |||||
chr2:202766102 | A | ACACC | 4 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0025 others(1): Show |
13 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*341_*342insCCAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 342 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | |||||
chr2:202766102 | A | ACC | 3 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0087 |
6 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*339_*340insCC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 340 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | |||||
chr2:202766102 | A | C | 1 | a0001c0001t0004 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 338 | chr2 | 202766102 | ||||||
chr2:202766180 | A | T | 1 | a0001c0001t0099 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*416A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 416 | chr2 | 202766180 | ||||||
chr2:202766636 | G | A | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(52): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*872G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 872 | chr2 | 202766636 | ||||||
chr2:202766645 | C | T | 9 | a0001c0001t0029 a0001c0001t0044 a0001c0001t0083 others(6): Show |
17 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*881C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 881 | chr2 | 202766645 | ||||||
chr2:202766646 | G | A | 1 | a0001c0001t0028 | 3 | HG02965.hp1 HG03579.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*882G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 882 | chr2 | 202766646 | ||||||
chr2:202766722 | T | C | 56 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(53): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*958T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 958 | chr2 | 202766722 | ||||||
chr2:202766724 | C | T | 32 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(29): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 960 | chr2 | 202766724 | ||||||
chr2:202766744 | T | G | 1 | a0001c0008t0074 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 980 | chr2 | 202766744 | ||||||
chr2:202766833 | G | A | 32 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(29): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1069 | chr2 | 202766833 | ||||||
chr2:202766860 | G | A | 1 | a0001c0001t0088 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1096G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1096 | chr2 | 202766860 | ||||||
chr2:202766898 | G | A | 1 | a0001c0001t0048 | 2 | NA18970.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1134 | chr2 | 202766898 | ||||||
chr2:202766972 | A | T | 1 | a0001c0001t0098 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1208A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1208 | chr2 | 202766972 | ||||||
chr2:202767085 | A | G | 1 | a0001c0001t0094 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1321A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1321 | chr2 | 202767085 | ||||||
chr2:202767157 | C | CT | 8 | a0001c0001t0010 a0001c0001t0064 a0001c0001t0078 others(5): Show |
12 | HG00544.hp1 HG01168.hp2 HG01943.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1413dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | |||||
chr2:202767157 | C | CTT | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(19): Show |
91 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1412_*1413dupTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | |||||
chr2:202767157 | C | CTTT | 4 | a0001c0001t0045 a0001c0001t0046 a0001c0001t0085 others(1): Show |
6 | HG02080.hp2 HG04199.hp1 HG04204.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1411_*1413dupTTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | |||||
chr2:202767157 | CT | C | 7 | a0001c0001t0026 a0001c0001t0030 a0001c0001t0040 others(4): Show |
12 | HG01346.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1413delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1413 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | |||||
chr2:202767157 | CTT | C | 50 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(47): Show |
118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1412_*1413delTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1412 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | |||||
chr2:202767182 | C | T | 1 | a0003c0003t0112 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1418 | chr2 | 202767182 | ||||||
chr2:202767217 | A | G | 1 | a0001c0001t0097 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1453 | chr2 | 202767217 | ||||||
chr2:202767344 | T | G | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1580T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1580 | chr2 | 202767344 | ||||||
chr2:202767461 | G | GGAGCAGC others(345): Show |
1 | a0002c0002t0071 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1713_*1714insTTTT others(348): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1714 | INFO_REALIGN_3_PRIME | chr2 | 202767461 | |||||
chr2:202767543 | A | T | 1 | a0001c0001t0063 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1779 | chr2 | 202767543 | ||||||
chr2:202767564 | C | T | 2 | a0001c0001t0107 a0001c0008t0074 |
2 | HG01884.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1800C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1800 | chr2 | 202767564 | ||||||
chr2:202767730 | C | A | 1 | a0001c0001t0092 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1966C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1966 | chr2 | 202767730 | ||||||
chr2:202767787 | T | C | 57 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(54): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2023 | chr2 | 202767787 | ||||||
chr2:202767882 | A | T | 2 | a0001c0001t0027 a0001c0001t0104 |
4 | HG02132.hp2 NA18969.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2118A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2118 | chr2 | 202767882 | ||||||
chr2:202768067 | G | A | 1 | a0001c0001t0106 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2303 | chr2 | 202768067 | ||||||
chr2:202768069 | A | G | 1 | a0001c0001t0106 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2305 | chr2 | 202768069 | ||||||
chr2:202768070 | G | GT | 32 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(29): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2308dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2309 | INFO_REALIGN_3_PRIME | chr2 | 202768070 | |||||
chr2:202768070 | G | T | 1 | a0001c0001t0106 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2306G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2306 | chr2 | 202768070 | ||||||
chr2:202768522 | A | C | 5 | a0001c0001t0042 a0001c0001t0090 a0001c0001t0102 others(2): Show |
6 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2758A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2758 | chr2 | 202768522 | ||||||
chr2:202768565 | T | C | 2 | a0001c0001t0095 a0001c0001t0100 |
2 | HG03130.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2801T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2801 | chr2 | 202768565 | ||||||
chr2:202769222 | T | G | 1 | a0001c0001t0093 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3458T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3458 | chr2 | 202769222 | ||||||
chr2:202769497 | A | G | 1 | a0001c0001t0089 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3733A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3733 | chr2 | 202769497 | ||||||
chr2:202769650 | A | G | 1 | a0001c0007t0068 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3886A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3886 | chr2 | 202769650 | ||||||
chr2:202769714 | G | A | 1 | a0001c0007t0068 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3950G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3950 | chr2 | 202769714 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635937 | C | G | 35 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+149C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202635937 | |||||||
chr2:202636002 | C | T | 1 | a0001c0001t0011g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.601+214C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636002 | |||||||
chr2:202636256 | A | G | 12 | a0001c0001t0015g0271 a0001c0001t0015g0275 a0001c0001t0015g0276 others(9): Show |
12 | HG00558.hp2 HG00597.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+468A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636256 | |||||||
chr2:202636277 | A | T | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+489A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636277 | |||||||
chr2:202636455 | A | G | 1 | a0001c0001t0050g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.601+667A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636455 | |||||||
chr2:202636716 | C | T | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+928C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636716 | |||||||
chr2:202636968 | C | T | 30 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.601+1180C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636968 | |||||||
chr2:202637041 | C | T | 3 | a0001c0001t0029g0268 a0001c0001t0029g0269 a0001c0001t0044g0267 |
3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+1253C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637041 | |||||||
chr2:202637123 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+1335C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637123 | |||||||
chr2:202637139 | C | T | 9 | a0001c0001t0025g0259 a0001c0001t0025g0261 a0001c0001t0042g0257 others(6): Show |
9 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+1351C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637139 | |||||||
chr2:202637148 | T | C | 41 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(38): Show |
41 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.601+1360T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637148 | |||||||
chr2:202637184 | A | C | 6 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0009g0256 others(3): Show |
6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+1396A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637184 | |||||||
chr2:202637445 | T | C | 35 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+1657T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637445 | |||||||
chr2:202637670 | T | C | 1 | a0001c0001t0013g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.601+1882T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637670 | |||||||
chr2:202637738 | A | G | 35 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+1950A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637738 | |||||||
chr2:202637873 | C | CT | 13 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0050g0270 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+2106dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202637873 | ||||||
chr2:202637873 | CT | C | 56 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(53): Show |
56 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.601+2106delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202637873 | ||||||
chr2:202637970 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+2182G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637970 | |||||||
chr2:202637981 | A | T | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+2193A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637981 | |||||||
chr2:202638127 | C | T | 1 | a0001c0001t0111g0244 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.601+2339C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638127 | |||||||
chr2:202638164 | A | G | 1 | a0001c0001t0105g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.601+2376A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638164 | |||||||
chr2:202638168 | C | T | 1 | a0001c0001t0027g0242 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+2380C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638168 | |||||||
chr2:202638369 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.601+2581A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638369 | |||||||
chr2:202638401 | T | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+2613T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638401 | |||||||
chr2:202638572 | AAAAT | A | 35 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+2805_601+2808d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202638572 | ||||||
chr2:202638740 | G | A | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+2952G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638740 | |||||||
chr2:202638889 | A | C | 35 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+3101A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638889 | |||||||
chr2:202638911 | C | T | 15 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+3123C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638911 | |||||||
chr2:202639072 | T | C | 1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.601+3284T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639072 | |||||||
chr2:202639146 | A | G | 1 | a0001c0001t0079g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.601+3358A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639146 | |||||||
chr2:202639231 | T | C | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+3443T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639231 | |||||||
chr2:202639301 | T | G | 7 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(4): Show |
7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+3513T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639301 | |||||||
chr2:202639375 | A | G | 1 | a0001c0001t0039g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.601+3587A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639375 | |||||||
chr2:202639378 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+3590C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639378 | |||||||
chr2:202639438 | C | T | 15 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+3650C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639438 | |||||||
chr2:202639665 | G | A | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+3877G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639665 | |||||||
chr2:202639786 | T | G | 1 | a0001c0001t0029g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.601+3998T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639786 | |||||||
chr2:202639992 | G | A | 5 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+4204G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639992 | |||||||
chr2:202640293 | A | AATATATA others(3): Show |
1 | a0001c0001t0119g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.601+4506_601+4507i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | A | AATATATA others(5): Show |
1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+4506_601+4507i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | A | AATATATA others(7): Show |
2 | a0001c0001t0004g0019 a0001c0001t0020g0032 |
2 | HG00741.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.601+4506_601+4507i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | AAAATAT | A | 8 | a0001c0001t0003g0133 a0001c0001t0004g0029 a0001c0001t0004g0045 others(5): Show |
8 | HG00609.hp1 HG00639.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+4507_601+4512d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | AAAATATA others(1): Show |
A | 3 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0019g0035 |
3 | HG00738.hp1 HG01099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4514d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | AAAATATA others(3): Show |
A | 3 | a0001c0001t0004g0027 a0001c0001t0019g0036 a0001c0001t0020g0030 |
3 | HG01106.hp1 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4516d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | AAAATATA others(5): Show |
A | 2 | a0001c0001t0019g0033 a0001c0001t0019g0034 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4518d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640293 | AAAATATA others(13): Show |
A | 2 | a0001c0001t0020g0021 a0001c0001t0020g0024 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.601+4507_601+4526d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | ||||||
chr2:202640295 | A | AAT | 28 | a0001c0001t0001g0172 a0001c0001t0001g0217 a0001c0001t0001g0241 others(25): Show |
28 | HG00408.hp1 HG00544.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+4554_601+4555d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATAT | 17 | a0001c0001t0001g0106 a0001c0001t0001g0139 a0001c0001t0001g0167 others(14): Show |
17 | HG00558.hp1 HG00597.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.601+4552_601+4555d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATAT | 16 | a0001c0001t0001g0061 a0001c0001t0001g0218 a0001c0001t0002g0173 others(13): Show |
16 | HG01975.hp2 HG02027.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.601+4550_601+4555d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(1): Show |
14 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0160 others(11): Show |
14 | HG00673.hp1 HG01168.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.601+4548_601+4555d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(3): Show |
10 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0005g0051 others(7): Show |
10 | HG01943.hp1 HG02132.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+4546_601+4555d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(5): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0163 a0001c0001t0022g0110 others(1): Show |
4 | HG00323.hp1 HG02155.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4544_601+4555d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(7): Show |
1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.601+4542_601+4555d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(11): Show |
1 | a0002c0002t0006g0314 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.601+4522_601+4523i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(13): Show |
2 | a0002c0002t0006g0312 a0002c0002t0006g0313 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601+4522_601+4523i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+4540_601+4555d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(11): Show |
5 | a0001c0001t0001g0136 a0001c0001t0001g0144 a0001c0001t0008g0221 others(2): Show |
5 | HG03098.hp1 HG03704.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+4538_601+4555d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | AATATATA others(15): Show |
1 | a0001c0001t0010g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.601+4534_601+4555d others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | A | ATATATAT | 3 | a0001c0001t0005g0203 a0001c0001t0031g0151 a0002c0002t0016g0299 |
3 | HG02723.hp1 NA18950.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4508i others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640295 | |||||||
chr2:202640295 | A | T | 9 | a0001c0001t0003g0191 a0001c0001t0004g0019 a0001c0001t0004g0020 others(6): Show |
9 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+4507A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640295 | |||||||
chr2:202640295 | AAT | A | 19 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0156 others(16): Show |
19 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.601+4554_601+4555d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATAT | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0220 a0001c0001t0026g0251 |
3 | HG01975.hp1 HG02155.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601+4552_601+4555d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATAT | A | 6 | a0001c0001t0005g0234 a0001c0001t0007g0072 a0001c0001t0009g0256 others(3): Show |
6 | HG00140.hp1 HG01346.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+4550_601+4555d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0154 a0001c0001t0003g0153 a0001c0001t0003g0158 others(6): Show |
9 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+4548_601+4555d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(3): Show |
A | 12 | a0001c0001t0001g0037 a0001c0001t0001g0105 a0001c0001t0001g0120 others(9): Show |
12 | HG00609.hp2 HG00621.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+4546_601+4555d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(5): Show |
A | 17 | a0001c0001t0001g0141 a0001c0001t0002g0065 a0001c0001t0002g0080 others(14): Show |
17 | HG00408.hp2 HG00597.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.601+4544_601+4555d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(7): Show |
A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0166 a0001c0001t0002g0054 others(49): Show |
52 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.601+4542_601+4555d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(9): Show |
A | 8 | a0001c0001t0015g0271 a0001c0001t0052g0274 a0001c0001t0053g0273 others(5): Show |
8 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+4540_601+4555d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(11): Show |
A | 6 | a0001c0001t0003g0149 a0003c0003t0012g0246 a0003c0003t0012g0247 others(3): Show |
6 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+4538_601+4555d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(13): Show |
A | 3 | a0001c0001t0029g0268 a0001c0001t0063g0288 a0001c0001t0083g0102 |
3 | HG02109.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+4536_601+4555d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(17): Show |
A | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+4532_601+4555d others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(25): Show |
A | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.601+4524_601+4555d others(34): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640295 | AATATATA others(29): Show |
A | 1 | a0001c0001t0080g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601+4520_601+4555d others(38): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | ||||||
chr2:202640299 | T | TATATATA others(5): Show |
1 | a0002c0002t0032g0294 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.601+4522_601+4523i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640299 | ||||||
chr2:202640329 | T | C | 1 | a0001c0001t0122g0009 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601+4541T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640329 | |||||||
chr2:202640340 | A | ATATATAT others(7): Show |
1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+4555_601+4556i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | ATATATAT others(5): Show |
1 | a0002c0002t0069g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+4555_601+4556i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | ATATATAT others(3): Show |
2 | a0002c0002t0006g0305 a0002c0002t0062g0304 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.601+4555_601+4556i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | ATATATG | 3 | a0002c0002t0006g0306 a0002c0002t0006g0307 a0002c0002t0006g0308 |
3 | HG02559.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.601+4555_601+4556i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | ATATG | 8 | a0002c0002t0006g0309 a0002c0002t0016g0296 a0002c0002t0016g0297 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+4553_601+4556d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | ATG | 4 | a0002c0002t0021g0290 a0002c0002t0021g0291 a0002c0002t0073g0292 others(1): Show |
4 | HG02970.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4553_601+4554i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | ||||||
chr2:202640340 | A | G | 10 | a0002c0002t0006g0312 a0002c0002t0006g0313 a0002c0002t0006g0314 others(7): Show |
10 | HG00733.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+4552A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640340 | |||||||
chr2:202640344 | G | A | 3 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0057g0205 |
3 | HG02145.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.601+4556G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640344 | |||||||
chr2:202640402 | A | G | 12 | a0001c0001t0005g0051 a0001c0001t0005g0234 a0001c0001t0005g0238 others(9): Show |
12 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+4614A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640402 | |||||||
chr2:202640447 | G | A | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+4659G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640447 | |||||||
chr2:202640462 | G | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+4674G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640462 | |||||||
chr2:202640470 | G | A | 3 | a0002c0002t0006g0312 a0002c0002t0006g0313 a0002c0002t0006g0314 |
3 | HG00733.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601+4682G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640470 | |||||||
chr2:202640803 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 others(1): Show |
4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+5015G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640803 | |||||||
chr2:202640874 | G | T | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+5086G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640874 | |||||||
chr2:202640907 | C | G | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5119C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640907 | |||||||
chr2:202641266 | T | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 others(1): Show |
4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+5478T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641266 | |||||||
chr2:202641315 | A | T | 1 | a0001c0001t0094g0230 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.601+5527A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641315 | |||||||
chr2:202641442 | A | G | 6 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+5654A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641442 | |||||||
chr2:202641475 | C | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5687C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641475 | |||||||
chr2:202641550 | T | G | 1 | a0003c0003t0032g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601+5762T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641550 | |||||||
chr2:202641554 | A | G | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+5766A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641554 | |||||||
chr2:202641641 | CT | C | 124 | a0001c0001t0001g0017 a0001c0001t0001g0060 a0001c0001t0001g0061 others(121): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.601+5868delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641641 | ||||||
chr2:202641641 | CTT | C | 34 | a0001c0001t0002g0054 a0001c0001t0036g0286 a0001c0001t0036g0287 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5867_601+5868d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641641 | ||||||
chr2:202641891 | G | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 others(1): Show |
4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6103G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641891 | |||||||
chr2:202641947 | C | CT | 10 | a0001c0001t0001g0220 a0001c0001t0008g0221 a0001c0001t0008g0224 others(7): Show |
10 | HG01952.hp2 HG02155.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+6174dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641947 | ||||||
chr2:202641965 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG02080.hp2 NA18962.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+6177C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641965 | |||||||
chr2:202642117 | C | CT | 8 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(5): Show |
8 | HG00609.hp1 HG02132.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+6346dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642117 | ||||||
chr2:202642344 | A | AAT | 11 | a0001c0001t0001g0215 a0001c0001t0002g0216 a0001c0001t0010g0018 others(8): Show |
11 | HG01168.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.601+6576_601+6577d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATAT | 17 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(14): Show |
17 | HG00544.hp2 HG00642.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.601+6574_601+6577d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATAT | 19 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(16): Show |
19 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+6572_601+6577d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATATA others(3): Show |
18 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(15): Show |
18 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.601+6568_601+6577d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATATA others(5): Show |
4 | a0002c0002t0006g0308 a0002c0002t0016g0297 a0002c0002t0037g0293 others(1): Show |
4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6566_601+6577d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATATA others(11): Show |
4 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(1): Show |
4 | HG01884.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+6560_601+6577d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATATA others(15): Show |
1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+6577_601+6578i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642344 | A | AATATATA others(21): Show |
1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+6577_601+6578i others(30): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | ||||||
chr2:202642541 | G | C | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601+6753G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642541 | |||||||
chr2:202642666 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.601+6878A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642666 | |||||||
chr2:202642701 | A | G | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+6913A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642701 | |||||||
chr2:202642759 | G | C | 3 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0003c0003t0010g0103 |
3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.601+6971G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642759 | |||||||
chr2:202642837 | A | C | 1 | a0001c0001t0008g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601+7049A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642837 | |||||||
chr2:202642940 | C | T | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+7152C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642940 | |||||||
chr2:202643157 | A | G | 4 | a0001c0001t0019g0033 a0001c0001t0019g0034 a0001c0001t0019g0035 others(1): Show |
4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+7369A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643157 | |||||||
chr2:202643263 | G | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+7475G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643263 | |||||||
chr2:202643344 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0105 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.601+7556G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643344 | |||||||
chr2:202643555 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+7767G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643555 | |||||||
chr2:202643910 | G | A | 12 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+8122G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643910 | |||||||
chr2:202644030 | G | A | 1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+8242G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644030 | |||||||
chr2:202644053 | G | GT | 24 | a0001c0001t0002g0065 a0001c0001t0002g0068 a0001c0001t0002g0071 others(21): Show |
24 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+8275dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTT | 23 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0077 others(20): Show |
23 | HG00558.hp2 HG01109.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.601+8274_601+8275d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTT | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(6): Show |
9 | HG00673.hp2 HG01884.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+8273_601+8275d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTT | 8 | a0001c0001t0002g0097 a0002c0002t0016g0296 a0002c0002t0016g0297 others(5): Show |
8 | HG00621.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+8271_601+8275d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTTTT others(3): Show |
4 | a0002c0002t0006g0305 a0002c0002t0032g0294 a0002c0002t0037g0293 others(1): Show |
4 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+8266_601+8275d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTTTT others(4): Show |
1 | a0002c0002t0069g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTTTT others(6): Show |
1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644053 | G | GTTTTTTT others(9): Show |
1 | a0002c0002t0006g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | ||||||
chr2:202644056 | T | TTTTTTTT others(6): Show |
1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644056 | ||||||
chr2:202644060 | T | TTTTTTTT others(6): Show |
3 | a0001c0001t0005g0003 a0001c0001t0028g0002 a0001c0001t0047g0006 |
3 | HG02257.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644060 | ||||||
chr2:202644064 | G | GT | 25 | a0001c0001t0001g0114 a0001c0001t0002g0173 a0001c0001t0002g0216 others(22): Show |
25 | HG00558.hp1 HG01975.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.601+8296dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | ||||||
chr2:202644064 | G | T | 101 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(98): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.601+8276G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644064 | |||||||
chr2:202644064 | GT | G | 7 | a0001c0001t0005g0051 a0001c0001t0005g0200 a0001c0001t0019g0036 others(4): Show |
7 | HG01891.hp1 HG02738.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+8296delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | ||||||
chr2:202644064 | GTT | G | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+8295_601+8296d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | ||||||
chr2:202644065 | T | G | 1 | a0002c0002t0062g0304 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.601+8277T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644065 | |||||||
chr2:202644074 | T | G | 4 | a0001c0001t0001g0038 a0001c0001t0009g0107 a0001c0001t0014g0108 others(1): Show |
4 | NA18948.hp2 NA18964.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+8286T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644074 | |||||||
chr2:202644075 | T | G | 1 | a0001c0001t0103g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601+8287T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644075 | |||||||
chr2:202644514 | T | C | 1 | a0001c0001t0022g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601+8726T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644514 | |||||||
chr2:202644521 | G | A | 1 | a0001c0001t0051g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.601+8733G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644521 | |||||||
chr2:202644722 | T | C | 7 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(4): Show |
7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+8934T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644722 | |||||||
chr2:202644835 | C | T | 14 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(11): Show |
14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+9047C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644835 | |||||||
chr2:202644898 | A | G | 6 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(3): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+9110A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644898 | |||||||
chr2:202645147 | T | G | 1 | a0003c0003t0012g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+9359T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645147 | |||||||
chr2:202645283 | C | CT | 8 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(5): Show |
8 | HG01952.hp2 HG02293.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+9506dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202645283 | ||||||
chr2:202645349 | C | T | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+9561C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645349 | |||||||
chr2:202645359 | G | A | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.601+9571G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645359 | |||||||
chr2:202645479 | C | T | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+9691C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645479 | |||||||
chr2:202645493 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+9705G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645493 | |||||||
chr2:202645493 | G | T | 1 | a0001c0001t0005g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.601+9705G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645493 | |||||||
chr2:202645533 | C | T | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601+9745C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645533 | |||||||
chr2:202645609 | GATTTATT others(1): Show |
G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | HG02080.hp2 NA18962.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+9826_601+9833d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202645609 | ||||||
chr2:202645701 | T | G | 1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+9913T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645701 | |||||||
chr2:202645780 | A | G | 1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+9992A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645780 | |||||||
chr2:202645837 | C | T | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+10049C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645837 | |||||||
chr2:202646031 | G | GT | 6 | a0001c0001t0001g0255 a0001c0001t0009g0256 a0001c0001t0010g0254 others(3): Show |
6 | HG02895.hp2 HG02965.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+10256dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202646031 | ||||||
chr2:202646034 | T | G | 1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+10246T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646034 | |||||||
chr2:202646050 | G | GA | 102 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(99): Show |
102 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.601+10262_601+1026 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646050 | |||||||
chr2:202646119 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.601+10331C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646119 | |||||||
chr2:202646122 | G | A | 1 | a0001c0001t0026g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.601+10334G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646122 | |||||||
chr2:202646137 | C | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+10349C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646137 | |||||||
chr2:202646254 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0217 |
2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601+10466G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646254 | |||||||
chr2:202646453 | C | A | 1 | a0001c0001t0045g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601+10665C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646453 | |||||||
chr2:202646622 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.601+10834C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646622 | |||||||
chr2:202646691 | T | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+10903T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646691 | |||||||
chr2:202646809 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601+11021C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646809 | |||||||
chr2:202646825 | A | G | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11037A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646825 | |||||||
chr2:202646840 | CTTGT | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11055_601+1105 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202646840 | ||||||
chr2:202646848 | A | C | 79 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(76): Show |
79 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.601+11060A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646848 | |||||||
chr2:202646917 | G | A | 2 | a0001c0004t0038g0012 a0001c0004t0038g0013 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.601+11129G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646917 | |||||||
chr2:202647023 | T | G | 3 | a0001c0001t0029g0268 a0001c0001t0029g0269 a0001c0001t0044g0267 |
3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+11235T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647023 | |||||||
chr2:202647415 | C | A | 26 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(23): Show |
26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.601+11627C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647415 | |||||||
chr2:202647420 | A | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11632A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647420 | |||||||
chr2:202647434 | A | T | 1 | a0001c0001t0101g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601+11646A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647434 | |||||||
chr2:202647436 | T | A | 1 | a0001c0001t0024g0177 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.601+11648T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647436 | |||||||
chr2:202647759 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+11971G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647759 | |||||||
chr2:202647843 | A | AT | 6 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0088 others(3): Show |
6 | HG00099.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+12062dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202647843 | ||||||
chr2:202647967 | C | T | 1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+12179C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647967 | |||||||
chr2:202648244 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.601+12456T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648244 | |||||||
chr2:202648518 | A | AC | 155 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.601+12740dupC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | ||||||
chr2:202648518 | A | ACC | 38 | a0001c0001t0001g0061 a0001c0001t0001g0166 a0001c0001t0001g0167 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.601+12739_601+1274 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | ||||||
chr2:202648518 | A | C | 2 | a0001c0001t0008g0226 a0001c0001t0047g0225 |
2 | HG01952.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.601+12730A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648518 | |||||||
chr2:202648518 | AC | A | 31 | a0001c0001t0026g0251 a0001c0001t0026g0252 a0002c0002t0006g0302 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+12740delC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | ||||||
chr2:202648529 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+12741A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648529 | |||||||
chr2:202648542 | C | CAT | 3 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0064g0284 |
3 | HG02723.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+12765_601+1276 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648542 | ||||||
chr2:202648542 | C | CATAT | 31 | a0001c0001t0063g0288 a0001c0007t0068g0285 a0002c0002t0006g0302 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+12763_601+1276 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648542 | ||||||
chr2:202648953 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.601+13165C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648953 | |||||||
chr2:202648973 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.601+13185C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648973 | |||||||
chr2:202648987 | C | T | 1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+13199C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648987 | |||||||
chr2:202649008 | C | CCT | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+13222_601+1322 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649008 | ||||||
chr2:202649106 | G | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+13318G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649106 | |||||||
chr2:202649297 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0009g0084 a0001c0001t0031g0083 |
3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.601+13509C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649297 | |||||||
chr2:202649303 | T | C | 1 | a0001c0001t0051g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601+13515T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649303 | |||||||
chr2:202649535 | GTTAT | G | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+13762_601+1376 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649535 | ||||||
chr2:202649760 | C | G | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.601+13972C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649760 | |||||||
chr2:202649858 | ATTTG | A | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+14086_601+1408 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649858 | ||||||
chr2:202649913 | G | A | 1 | a0001c0001t0031g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.601+14125G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649913 | |||||||
chr2:202649930 | C | T | 3 | a0001c0001t0002g0071 a0001c0001t0003g0070 a0001c0001t0043g0069 |
3 | HG02165.hp2 NA18954.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.601+14142C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649930 | |||||||
chr2:202650898 | C | T | 3 | a0001c0001t0029g0268 a0001c0001t0029g0269 a0001c0001t0044g0267 |
3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+15110C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202650898 | |||||||
chr2:202650929 | T | C | 3 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0003c0003t0010g0103 |
3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.601+15141T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202650929 | |||||||
chr2:202651013 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0101g0174 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+15225G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651013 | |||||||
chr2:202651060 | CT | C | 137 | a0001c0001t0001g0017 a0001c0001t0001g0120 a0001c0001t0001g0163 others(134): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.601+15292delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202651060 | ||||||
chr2:202651060 | CTT | C | 7 | a0001c0001t0015g0271 a0001c0001t0054g0272 a0001c0004t0038g0012 others(4): Show |
7 | HG01167.hp2 HG01168.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+15291_601+1529 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202651060 | ||||||
chr2:202651080 | T | A | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+15292T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651080 | |||||||
chr2:202651218 | C | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+15430C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651218 | |||||||
chr2:202651264 | G | A | 4 | a0001c0001t0019g0033 a0001c0001t0019g0034 a0001c0001t0019g0035 others(1): Show |
4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+15476G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651264 | |||||||
chr2:202651376 | C | T | 145 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(142): Show |
145 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.601+15588C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651376 | |||||||
chr2:202651409 | G | T | 1 | a0001c0001t0055g0282 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.601+15621G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651409 | |||||||
chr2:202651512 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.601+15724A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651512 | |||||||
chr2:202651523 | C | T | 1 | a0001c0001t0100g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.601+15735C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651523 | |||||||
chr2:202651588 | G | A | 1 | a0001c0001t0109g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.601+15800G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651588 | |||||||
chr2:202651769 | A | G | 1 | a0002c0002t0069g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+15981A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651769 | |||||||
chr2:202651829 | G | A | 14 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(11): Show |
14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+16041G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651829 | |||||||
chr2:202651834 | A | G | 5 | a0001c0001t0001g0255 a0001c0001t0009g0256 a0001c0001t0010g0254 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+16046A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651834 | |||||||
chr2:202651839 | A | G | 1 | a0001c0001t0007g0014 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.601+16051A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651839 | |||||||
chr2:202651909 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0023g0159 |
2 | HG00673.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.601+16121C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651909 | |||||||
chr2:202651947 | G | A | 1 | a0001c0001t0011g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.601+16159G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651947 | |||||||
chr2:202652034 | C | A | 1 | a0001c0001t0005g0234 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.601+16246C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652034 | |||||||
chr2:202652052 | T | TA | 9 | a0001c0001t0004g0019 a0001c0001t0005g0003 a0001c0001t0008g0004 others(6): Show |
9 | HG00544.hp2 HG01981.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+16284dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202652052 | ||||||
chr2:202652052 | TA | T | 46 | a0001c0001t0001g0117 a0001c0001t0001g0172 a0001c0001t0001g0220 others(43): Show |
46 | HG00733.hp1 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.601+16284delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202652052 | ||||||
chr2:202652086 | G | A | 2 | a0001c0001t0018g0181 a0001c0001t0018g0182 |
2 | NA18980.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.601+16298G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652086 | |||||||
chr2:202652183 | C | T | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+16395C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652183 | |||||||
chr2:202652210 | C | T | 1 | a0001c0001t0106g0212 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.601+16422C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652210 | |||||||
chr2:202652245 | C | A | 1 | a0001c0001t0098g0044 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.601+16457C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652245 | |||||||
chr2:202652328 | T | C | 2 | a0001c0001t0002g0065 a0001c0006t0110g0064 |
2 | NA18949.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.601+16540T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652328 | |||||||
chr2:202652488 | A | G | 1 | a0001c0001t0113g0263 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.601+16700A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652488 | |||||||
chr2:202652572 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+16784T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652572 | |||||||
chr2:202652723 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+16935G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652723 | |||||||
chr2:202652864 | G | A | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.601+17076G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652864 | |||||||
chr2:202652878 | C | A | 1 | a0001c0001t0009g0119 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.601+17090C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652878 | |||||||
chr2:202653171 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+17383G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653171 | |||||||
chr2:202653318 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+17530G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653318 | |||||||
chr2:202653400 | C | T | 3 | a0001c0001t0029g0268 a0001c0001t0029g0269 a0001c0001t0044g0267 |
3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+17612C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653400 | |||||||
chr2:202653406 | G | A | 1 | a0001c0001t0023g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.601+17618G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653406 | |||||||
chr2:202653550 | A | G | 2 | a0001c0001t0009g0119 a0001c0001t0031g0157 |
2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.601+17762A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653550 | |||||||
chr2:202653723 | G | A | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+17935G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653723 | |||||||
chr2:202653774 | G | A | 2 | a0001c0001t0024g0177 a0002c0002t0067g0315 |
2 | HG00099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.601+17986G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653774 | |||||||
chr2:202653997 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.601+18209C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653997 | |||||||
chr2:202654062 | T | A | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+18274T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654062 | |||||||
chr2:202654062 | T | TGA | 63 | a0001c0001t0001g0123 a0001c0001t0001g0196 a0001c0001t0001g0215 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.601+18308_601+1830 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | T | TGAGA | 15 | a0001c0001t0002g0058 a0001c0001t0002g0090 a0001c0001t0003g0089 others(12): Show |
15 | HG00673.hp2 HG01106.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.601+18306_601+1830 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | T | TGAGTGAG others(1): Show |
5 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18277_601+1827 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | T | TGAGTGAG others(3): Show |
1 | a0001c0001t0047g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.601+18277_601+1827 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGA | T | 4 | a0001c0001t0001g0155 a0001c0001t0020g0032 a0001c0001t0022g0110 others(1): Show |
4 | HG00621.hp2 HG00741.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+18308_601+1830 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGAGA | T | 29 | a0001c0001t0002g0054 a0001c0001t0002g0081 a0001c0001t0002g0092 others(26): Show |
29 | HG00621.hp1 HG00738.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+18306_601+1830 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGAGAGAG others(1): Show |
T | 31 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+18302_601+1830 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGAGAGAG others(3): Show |
T | 2 | a0001c0001t0005g0118 a0001c0001t0101g0174 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+18300_601+1830 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGAGAGAG others(5): Show |
T | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18298_601+1830 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654062 | TGAGAGAG others(7): Show |
T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+18296_601+1830 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | ||||||
chr2:202654066 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.601+18278A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654066 | |||||||
chr2:202654161 | AAGAC | A | 33 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0003g0153 others(30): Show |
33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.601+18376_601+1837 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654161 | ||||||
chr2:202654262 | C | CA | 71 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(68): Show |
71 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.601+18486dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654262 | ||||||
chr2:202654263 | A | C | 1 | a0001c0001t0034g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.601+18475A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654263 | |||||||
chr2:202654527 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+18739G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654527 | |||||||
chr2:202654541 | G | T | 26 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(23): Show |
26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.601+18753G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654541 | |||||||
chr2:202654632 | T | G | 1 | a0001c0001t0019g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601+18844T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654632 | |||||||
chr2:202654665 | CT | C | 10 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0088 others(7): Show |
10 | HG00099.hp1 HG01071.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+18891delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654665 | ||||||
chr2:202654772 | C | T | 1 | a0001c0001t0031g0151 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.601+18984C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654772 | |||||||
chr2:202654870 | C | A | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19082C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654870 | |||||||
chr2:202655060 | T | G | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+19272T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655060 | |||||||
chr2:202655077 | A | AAATT | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19291_601+1929 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655077 | ||||||
chr2:202655099 | T | C | 1 | a0001c0001t0027g0242 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+19311T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655099 | |||||||
chr2:202655122 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19334G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655122 | |||||||
chr2:202655250 | G | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19462G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655250 | |||||||
chr2:202655317 | A | C | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+19529A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655317 | |||||||
chr2:202655549 | A | G | 247 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(244): Show |
247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.601+19761A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655549 | |||||||
chr2:202655552 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19764T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655552 | |||||||
chr2:202655625 | T | G | 1 | a0001c0001t0027g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.601+19837T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655625 | |||||||
chr2:202655697 | G | A | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(25): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+19909G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655697 | |||||||
chr2:202655707 | T | TGA | 5 | a0001c0001t0005g0238 a0001c0001t0008g0189 a0001c0001t0087g0190 others(2): Show |
5 | HG01256.hp1 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19973_601+1997 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | T | TGAGA | 4 | a0001c0001t0003g0186 a0001c0001t0010g0254 a0001c0001t0017g0187 others(1): Show |
4 | HG02523.hp1 HG02965.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19971_601+1997 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | T | TGAGAGAC others(1): Show |
8 | a0001c0001t0004g0045 a0001c0001t0019g0034 a0001c0001t0019g0035 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | T | TGAGAGAC others(3): Show |
4 | a0001c0001t0004g0020 a0001c0001t0004g0026 a0001c0001t0004g0101 others(1): Show |
4 | HG02056.hp1 HG02738.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | T | TGAGAGAC others(5): Show |
2 | a0001c0001t0004g0228 a0001c0001t0019g0033 |
2 | HG01433.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.601+19925_601+1992 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | T | TGAGAGAC others(7): Show |
1 | a0001c0001t0122g0009 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601+19925_601+1992 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGA | T | 51 | a0001c0001t0001g0166 a0001c0001t0002g0088 a0001c0001t0002g0091 others(48): Show |
51 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.601+19973_601+1997 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGA | T | 65 | a0001c0001t0001g0136 a0001c0001t0002g0054 a0001c0001t0002g0065 others(62): Show |
65 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.601+19971_601+1997 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGA | T | 51 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0060 others(48): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.601+19969_601+1997 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(1): Show |
T | 24 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0105 others(21): Show |
24 | HG00741.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+19967_601+1997 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(3): Show |
T | 8 | a0001c0001t0002g0058 a0001c0001t0003g0158 a0001c0001t0005g0122 others(5): Show |
8 | HG01081.hp1 HG01975.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+19965_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(5): Show |
T | 6 | a0001c0001t0002g0216 a0001c0001t0009g0165 a0001c0001t0080g0150 others(3): Show |
6 | HG00544.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+19963_601+1997 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(7): Show |
T | 12 | a0001c0001t0057g0205 a0002c0002t0016g0296 a0002c0002t0016g0299 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19961_601+1997 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(9): Show |
T | 3 | a0001c0001t0049g0209 a0002c0002t0059g0316 a0002c0002t0060g0317 |
3 | HG03098.hp2 HG03471.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.601+19959_601+1997 others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(11): Show |
T | 15 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+19957_601+1997 others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655707 | TGAGAGAG others(15): Show |
T | 1 | a0001c0001t0026g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.601+19953_601+1997 others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | ||||||
chr2:202655708 | G | GAGAGAC | 5 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(2): Show |
5 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655708 | ||||||
chr2:202655710 | G | GAGAC | 5 | a0001c0001t0004g0019 a0001c0001t0042g0257 a0001c0001t0072g0025 others(2): Show |
5 | HG01261.hp2 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655710 | ||||||
chr2:202655712 | G | GAC | 4 | a0001c0001t0004g0031 a0001c0001t0026g0124 a0001c0001t0064g0284 others(1): Show |
4 | HG00738.hp1 HG02723.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655712 | ||||||
chr2:202655714 | G | C | 24 | a0001c0001t0004g0022 a0001c0001t0005g0003 a0001c0001t0007g0094 others(21): Show |
24 | HG00558.hp2 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+19926G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655714 | |||||||
chr2:202655716 | G | C | 38 | a0001c0001t0001g0166 a0001c0001t0002g0088 a0001c0001t0002g0091 others(35): Show |
38 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.601+19928G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655716 | |||||||
chr2:202655718 | G | C | 53 | a0001c0001t0001g0136 a0001c0001t0002g0054 a0001c0001t0002g0065 others(50): Show |
53 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.601+19930G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655718 | |||||||
chr2:202655720 | G | C | 41 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0060 others(38): Show |
41 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.601+19932G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655720 | |||||||
chr2:202655722 | G | C | 22 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0105 others(19): Show |
22 | HG00741.hp1 HG01123.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.601+19934G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655722 | |||||||
chr2:202655724 | G | C | 8 | a0001c0001t0002g0058 a0001c0001t0003g0158 a0001c0001t0010g0104 others(5): Show |
8 | HG01081.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+19936G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655724 | |||||||
chr2:202655726 | G | C | 7 | a0001c0001t0001g0164 a0001c0001t0002g0216 a0001c0001t0009g0165 others(4): Show |
7 | HG01243.hp2 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+19938G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655726 | |||||||
chr2:202655728 | G | C | 11 | a0002c0002t0016g0296 a0002c0002t0016g0299 a0002c0002t0021g0289 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.601+19940G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655728 | |||||||
chr2:202655730 | G | C | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+19942G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655730 | |||||||
chr2:202655732 | G | C | 15 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+19944G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655732 | |||||||
chr2:202655741 | A | T | 1 | a0001c0001t0046g0121 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.601+19953A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655741 | |||||||
chr2:202655747 | A | T | 2 | a0001c0001t0036g0287 a0001c0001t0064g0284 |
2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+19959A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655747 | |||||||
chr2:202655749 | A | T | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19961A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655749 | |||||||
chr2:202655751 | A | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19963A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655751 | |||||||
chr2:202655753 | A | T | 6 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(3): Show |
6 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+19965A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655753 | |||||||
chr2:202655753 | AGAGAGAG others(3): Show |
A | 2 | a0001c0001t0028g0002 a0001c0001t0047g0006 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+19967_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655753 | ||||||
chr2:202655755 | A | T | 12 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(9): Show |
12 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19967A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655755 | |||||||
chr2:202655755 | AGAGAGAG others(1): Show |
A | 3 | a0001c0001t0020g0030 a0003c0003t0012g0062 a0003c0003t0012g0248 |
3 | HG01106.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601+19969_601+1997 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655755 | ||||||
chr2:202655755 | AGAGAGAG others(3): Show |
A | 1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+19969_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655755 | ||||||
chr2:202655757 | A | T | 12 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(9): Show |
12 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19969A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655757 | |||||||
chr2:202655759 | A | T | 30 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0045g0112 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.601+19971A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655759 | |||||||
chr2:202655761 | A | T | 48 | a0001c0001t0005g0051 a0001c0001t0008g0221 a0001c0001t0008g0224 others(45): Show |
48 | HG00558.hp1 HG00733.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.601+19973A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655761 | |||||||
chr2:202655763 | T | A | 5 | a0001c0001t0004g0031 a0001c0001t0005g0003 a0001c0001t0020g0021 others(2): Show |
5 | HG00738.hp1 HG01884.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19975T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655763 | |||||||
chr2:202655765 | T | A | 1 | a0003c0003t0032g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601+19977T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655765 | |||||||
chr2:202655994 | C | A | 1 | a0001c0001t0014g0219 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.601+20206C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655994 | |||||||
chr2:202656001 | G | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+20213G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656001 | |||||||
chr2:202656106 | A | G | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601+20318A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656106 | |||||||
chr2:202656262 | G | A | 1 | a0001c0001t0040g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.601+20474G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656262 | |||||||
chr2:202656274 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.601+20486C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656274 | |||||||
chr2:202656444 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+20656T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656444 | |||||||
chr2:202656468 | G | A | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+20680G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656468 | |||||||
chr2:202656623 | G | C | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+20835G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656623 | |||||||
chr2:202656755 | A | T | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+20967A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656755 | |||||||
chr2:202656762 | T | A | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+20974T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656762 | |||||||
chr2:202656851 | G | A | 1 | a0001c0001t0022g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601+21063G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656851 | |||||||
chr2:202656910 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+21122A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656910 | |||||||
chr2:202656989 | A | C | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601+21201A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656989 | |||||||
chr2:202657007 | A | G | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.601+21219A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657007 | |||||||
chr2:202657055 | ATTG | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+21271_601+2127 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202657055 | ||||||
chr2:202657087 | T | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+21299T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657087 | |||||||
chr2:202657484 | T | C | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+21696T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657484 | |||||||
chr2:202657561 | C | T | 14 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(11): Show |
14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+21773C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657561 | |||||||
chr2:202657607 | G | A | 1 | a0001c0001t0031g0157 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.601+21819G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657607 | |||||||
chr2:202657626 | C | T | 148 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.601+21838C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657626 | |||||||
chr2:202657819 | A | C | 1 | a0001c0001t0026g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.601+22031A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657819 | |||||||
chr2:202657832 | C | T | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+22044C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657832 | |||||||
chr2:202658319 | A | G | 67 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.601+22531A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658319 | |||||||
chr2:202658720 | C | T | 1 | a0001c0001t0055g0282 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.601+22932C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658720 | |||||||
chr2:202658805 | A | G | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.601+23017A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658805 | |||||||
chr2:202659297 | C | T | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+23509C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659297 | |||||||
chr2:202659341 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+23553G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659341 | |||||||
chr2:202659591 | G | A | 2 | a0001c0001t0002g0065 a0001c0006t0110g0064 |
2 | NA18949.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.601+23803G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659591 | |||||||
chr2:202659604 | C | CT | 77 | a0001c0001t0001g0043 a0001c0001t0001g0114 a0001c0001t0001g0117 others(74): Show |
77 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.601+23846dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | C | CTT | 31 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0105 others(28): Show |
31 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.601+23845_601+2384 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | C | CTTT | 8 | a0001c0001t0001g0061 a0001c0001t0001g0163 a0001c0001t0003g0142 others(5): Show |
8 | HG01175.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+23844_601+2384 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTT | C | 6 | a0001c0001t0002g0054 a0001c0001t0002g0058 a0001c0001t0002g0081 others(3): Show |
6 | NA18940.hp2 NA18946.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+23841_601+2384 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT | C | 62 | a0001c0001t0001g0017 a0001c0001t0002g0065 a0001c0001t0002g0068 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.601+23840_601+2384 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+23839_601+2384 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0013g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.601+23836_601+2384 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0005g0122 a0001c0001t0029g0268 a0001c0001t0029g0269 |
3 | HG01975.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+23835_601+2384 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+23834_601+2384 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659604 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0042g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.601+23826_601+2384 others(25): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | ||||||
chr2:202659911 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0003g0133 a0001c0001t0041g0138 |
3 | HG02165.hp1 NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.601+24123G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659911 | |||||||
chr2:202659918 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+24130C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659918 | |||||||
chr2:202660287 | A | G | 1 | a0001c0001t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601+24499A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660287 | |||||||
chr2:202660383 | C | T | 1 | a0001c0001t0004g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+24595C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660383 | |||||||
chr2:202660699 | A | G | 3 | a0001c0001t0019g0033 a0001c0001t0019g0035 a0001c0001t0019g0036 |
3 | HG01167.hp1 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.601+24911A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660699 | |||||||
chr2:202660711 | A | G | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.601+24923A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660711 | |||||||
chr2:202660790 | C | G | 1 | a0001c0001t0034g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601+25002C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660790 | |||||||
chr2:202661057 | G | A | 2 | a0003c0003t0012g0062 a0003c0003t0012g0248 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601+25269G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661057 | |||||||
chr2:202661245 | A | G | 69 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.601+25457A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661245 | |||||||
chr2:202661251 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.601+25463G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661251 | |||||||
chr2:202661457 | G | A | 1 | a0001c0001t0014g0219 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.601+25669G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661457 | |||||||
chr2:202661586 | C | T | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601+25798C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661586 | |||||||
chr2:202661661 | A | G | 1 | a0001c0001t0049g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.601+25873A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661661 | |||||||
chr2:202661744 | C | T | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+25956C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661744 | |||||||
chr2:202661751 | C | T | 1 | a0001c0001t0004g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+25963C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661751 | |||||||
chr2:202661777 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0043g0099 |
2 | NA18747.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.601+25989A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661777 | |||||||
chr2:202661780 | G | A | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+25992G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661780 | |||||||
chr2:202661864 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26076C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661864 | |||||||
chr2:202661919 | T | TA | 34 | a0001c0001t0003g0186 a0001c0001t0007g0066 a0001c0001t0015g0276 others(31): Show |
34 | HG00544.hp2 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.601+26150dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202661919 | ||||||
chr2:202661919 | TA | T | 6 | a0001c0001t0001g0220 a0001c0001t0002g0140 a0001c0001t0010g0214 others(3): Show |
6 | HG01891.hp1 HG02155.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+26150delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202661919 | ||||||
chr2:202662036 | C | G | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26248C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662036 | |||||||
chr2:202662089 | C | T | 1 | a0001c0001t0010g0011 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.601+26301C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662089 | |||||||
chr2:202662119 | G | GGT | 100 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(97): Show |
100 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.601+26350_601+2635 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202662119 | ||||||
chr2:202662119 | GGT | G | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26350_601+2635 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202662119 | ||||||
chr2:202662136 | G | A | 1 | a0001c0001t0109g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.601+26348G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662136 | |||||||
chr2:202662252 | G | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0136 a0001c0001t0002g0140 others(3): Show |
6 | HG02027.hp2 NA18951.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+26464G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662252 | |||||||
chr2:202662428 | T | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+26640T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662428 | |||||||
chr2:202662583 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+26795C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662583 | |||||||
chr2:202662592 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601+26804C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662592 | |||||||
chr2:202662758 | T | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+26970T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662758 | |||||||
chr2:202663256 | T | C | 177 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(174): Show |
177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.601+27468T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663256 | |||||||
chr2:202663580 | C | CT | 166 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0060 others(163): Show |
166 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.601+27807dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202663580 | ||||||
chr2:202663604 | A | G | 4 | a0001c0001t0024g0222 a0001c0001t0040g0195 a0001c0001t0040g0208 others(1): Show |
4 | HG02293.hp1 HG02300.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+27816A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663604 | |||||||
chr2:202663767 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.601+27979G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663767 | |||||||
chr2:202663773 | G | A | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+27985G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663773 | |||||||
chr2:202663836 | G | A | 1 | a0001c0001t0008g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.601+28048G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663836 | |||||||
chr2:202663995 | T | C | 1 | a0003c0003t0012g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601+28207T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663995 | |||||||
chr2:202664104 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0217 |
2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601+28316T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664104 | |||||||
chr2:202664159 | T | G | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+28371T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664159 | |||||||
chr2:202664346 | CAT | C | 10 | a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0080 others(7): Show |
10 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+28560_601+2856 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202664346 | ||||||
chr2:202664447 | G | A | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+28659G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664447 | |||||||
chr2:202664463 | A | G | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+28675A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664463 | |||||||
chr2:202664738 | C | T | 4 | a0001c0001t0009g0165 a0001c0001t0009g0169 a0001c0001t0080g0150 others(1): Show |
4 | HG01243.hp2 HG01255.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+28950C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664738 | |||||||
chr2:202664787 | T | A | 1 | a0003c0003t0012g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+28999T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664787 | |||||||
chr2:202664838 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+29050A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664838 | |||||||
chr2:202664940 | A | G | 1 | a0001c0001t0094g0230 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.601+29152A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664940 | |||||||
chr2:202665558 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+29770T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665558 | |||||||
chr2:202665609 | T | C | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+29821T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665609 | |||||||
chr2:202665815 | G | A | 10 | a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0080 others(7): Show |
10 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+30027G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665815 | |||||||
chr2:202665864 | G | A | 1 | a0001c0001t0041g0193 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.602-30017G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665864 | |||||||
chr2:202666403 | C | T | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-29478C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666403 | |||||||
chr2:202666500 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-29381T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666500 | |||||||
chr2:202666614 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.602-29267C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666614 | |||||||
chr2:202666668 | C | CT | 31 | a0001c0001t0001g0172 a0001c0001t0008g0224 a0001c0001t0008g0226 others(28): Show |
31 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.602-29195dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202666668 | ||||||
chr2:202666668 | C | CTT | 17 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(14): Show |
17 | HG00733.hp1 HG01109.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.602-29196_602-2919 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202666668 | ||||||
chr2:202666690 | A | G | 1 | a0001c0001t0005g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.602-29191A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666690 | |||||||
chr2:202666699 | C | T | 30 | a0001c0001t0005g0206 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-29182C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666699 | |||||||
chr2:202666923 | G | A | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-28958G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666923 | |||||||
chr2:202666974 | A | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-28907A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666974 | |||||||
chr2:202666987 | G | C | 8 | a0001c0001t0002g0054 a0001c0001t0002g0081 a0001c0001t0002g0092 others(5): Show |
8 | HG00621.hp1 NA18940.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-28894G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666987 | |||||||
chr2:202667163 | C | T | 1 | a0001c0001t0009g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-28718C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667163 | |||||||
chr2:202667173 | T | G | 1 | a0001c0001t0028g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.602-28708T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667173 | |||||||
chr2:202667212 | T | A | 70 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(67): Show |
70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-28669T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667212 | |||||||
chr2:202667347 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-28534C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667347 | |||||||
chr2:202667392 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.602-28489C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667392 | |||||||
chr2:202667446 | A | G | 33 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(30): Show |
33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.602-28435A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667446 | |||||||
chr2:202667454 | C | G | 1 | a0002c0002t0061g0310 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.602-28427C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667454 | |||||||
chr2:202667492 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.602-28389G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667492 | |||||||
chr2:202667581 | A | G | 70 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(67): Show |
70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-28300A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667581 | |||||||
chr2:202667846 | G | T | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-28035G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667846 | |||||||
chr2:202668004 | C | T | 6 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-27877C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668004 | |||||||
chr2:202668069 | A | G | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-27812A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668069 | |||||||
chr2:202668075 | A | G | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(96): Show |
99 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.602-27806A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668075 | |||||||
chr2:202668094 | A | AATATATT | 27 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(24): Show |
27 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-27786_602-2778 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668094 | ||||||
chr2:202668101 | T | TA | 6 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27780_602-2777 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668101 | |||||||
chr2:202668106 | T | TTTATA | 6 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27775_602-2777 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668106 | |||||||
chr2:202668107 | A | T | 6 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27774A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668107 | |||||||
chr2:202668155 | TA | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-27724delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668155 | ||||||
chr2:202668172 | CATATT | C | 28 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(25): Show |
28 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-27699_602-2769 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668172 | ||||||
chr2:202668202 | ATTT | A | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-27676_602-2767 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668202 | ||||||
chr2:202668233 | T | G | 1 | a0001c0001t0080g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602-27648T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668233 | |||||||
chr2:202668281 | A | G | 1 | a0001c0001t0022g0194 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.602-27600A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668281 | |||||||
chr2:202668412 | C | T | 1 | a0001c0001t0010g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.602-27469C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668412 | |||||||
chr2:202668514 | C | T | 1 | a0001c0001t0009g0010 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-27367C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668514 | |||||||
chr2:202668527 | C | CA | 77 | a0001c0001t0001g0017 a0001c0001t0001g0172 a0001c0001t0002g0054 others(74): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.602-27335dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | ||||||
chr2:202668527 | C | CAA | 25 | a0001c0001t0002g0080 a0001c0006t0110g0064 a0002c0002t0006g0305 others(22): Show |
25 | HG00733.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.602-27336_602-2733 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | ||||||
chr2:202668527 | CA | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0241 a0001c0001t0003g0042 others(5): Show |
8 | HG00140.hp2 HG02698.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-27335delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | ||||||
chr2:202668539 | A | G | 3 | a0001c0001t0029g0268 a0001c0001t0029g0269 a0001c0001t0044g0267 |
3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-27342A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668539 | |||||||
chr2:202668542 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.602-27339A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668542 | |||||||
chr2:202668543 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0014g0131 a0001c0001t0096g0148 |
3 | HG01358.hp1 HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.602-27338A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668543 | |||||||
chr2:202668578 | T | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-27303T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668578 | |||||||
chr2:202668620 | T | A | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-27261T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668620 | |||||||
chr2:202668620 | T | TAATA | 49 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0186 others(46): Show |
49 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.602-27230_602-2722 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668620 | ||||||
chr2:202668620 | TAATA | T | 107 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(104): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.602-27230_602-2722 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668620 | ||||||
chr2:202669198 | A | G | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-26683A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669198 | |||||||
chr2:202669517 | C | T | 4 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-26364C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669517 | |||||||
chr2:202669809 | T | G | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-26072T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669809 | |||||||
chr2:202670062 | T | G | 1 | a0001c0001t0042g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.602-25819T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670062 | |||||||
chr2:202670176 | G | T | 1 | a0001c0001t0005g0234 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.602-25705G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670176 | |||||||
chr2:202670237 | A | C | 6 | a0001c0001t0005g0234 a0001c0001t0018g0232 a0001c0001t0027g0233 others(3): Show |
6 | HG02132.hp2 NA18966.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-25644A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670237 | |||||||
chr2:202670257 | C | G | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-25624C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670257 | |||||||
chr2:202670298 | TC | T | 32 | a0001c0001t0063g0288 a0001c0001t0064g0284 a0001c0007t0068g0285 others(29): Show |
32 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.602-25582delC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670298 | |||||||
chr2:202670299 | C | T | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-25582C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670299 | |||||||
chr2:202670352 | C | T | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-25529C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670352 | |||||||
chr2:202670427 | T | A | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-25454T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670427 | |||||||
chr2:202670634 | A | G | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-25247A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670634 | |||||||
chr2:202670763 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0167 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.602-25118T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670763 | |||||||
chr2:202671025 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-24856A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671025 | |||||||
chr2:202671092 | C | T | 146 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.602-24789C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671092 | |||||||
chr2:202671158 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602-24723G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671158 | |||||||
chr2:202671177 | A | G | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-24704A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671177 | |||||||
chr2:202671224 | A | T | 2 | a0001c0001t0008g0049 a0001c0001t0017g0050 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.602-24657A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671224 | |||||||
chr2:202671362 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-24519C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671362 | |||||||
chr2:202671597 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-24284C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671597 | |||||||
chr2:202671738 | A | G | 1 | a0002c0002t0066g0300 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-24143A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671738 | |||||||
chr2:202671798 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.602-24083C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671798 | |||||||
chr2:202671944 | T | G | 1 | a0001c0001t0014g0108 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.602-23937T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671944 | |||||||
chr2:202672251 | C | A | 5 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-23630C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672251 | |||||||
chr2:202672258 | G | A | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-23623G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672258 | |||||||
chr2:202672281 | C | T | 1 | a0001c0001t0029g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.602-23600C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672281 | |||||||
chr2:202672282 | G | A | 3 | a0001c0001t0013g0008 a0001c0001t0013g0041 a0001c0001t0013g0137 |
3 | HG00609.hp2 HG01192.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.602-23599G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672282 | |||||||
chr2:202672340 | G | A | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-23541G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672340 | |||||||
chr2:202672420 | C | T | 1 | a0001c0001t0095g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-23461C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672420 | |||||||
chr2:202672570 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-23311G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672570 | |||||||
chr2:202672817 | T | A | 1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.602-23064T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672817 | |||||||
chr2:202672921 | A | T | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-22960A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672921 | |||||||
chr2:202672948 | T | C | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-22933T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672948 | |||||||
chr2:202672980 | C | T | 1 | a0001c0001t0010g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.602-22901C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672980 | |||||||
chr2:202673433 | G | GT | 30 | a0001c0001t0001g0123 a0001c0001t0001g0196 a0001c0001t0001g0220 others(27): Show |
30 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-22416dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTT | 12 | a0001c0001t0003g0042 a0001c0001t0008g0226 a0001c0001t0017g0040 others(9): Show |
12 | HG01081.hp2 HG02293.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-22417_602-2241 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTTTT | 6 | a0001c0001t0005g0234 a0001c0001t0005g0238 a0001c0001t0008g0049 others(3): Show |
6 | HG00738.hp2 HG01943.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-22419_602-2241 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTTTTT | 8 | a0001c0001t0005g0051 a0001c0001t0027g0233 a0001c0001t0027g0235 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-22420_602-2241 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTTTTTTT | 9 | a0002c0002t0006g0312 a0002c0002t0006g0313 a0002c0002t0032g0294 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-22422_602-2241 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTTTTTTT others(1): Show |
10 | a0002c0002t0006g0306 a0002c0002t0006g0307 a0002c0002t0006g0308 others(7): Show |
10 | HG00733.hp1 HG01243.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.602-22423_602-2241 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0064g0284 a0002c0002t0058g0318 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.602-22425_602-2241 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GT | G | 72 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0061 others(69): Show |
72 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.602-22416delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GTT | G | 12 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0152 others(9): Show |
12 | HG00544.hp2 HG01975.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-22417_602-2241 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GTTTT | G | 8 | a0001c0001t0002g0085 a0001c0001t0002g0088 a0001c0001t0002g0090 others(5): Show |
8 | HG01099.hp2 HG01175.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-22419_602-2241 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GTTTTT | G | 74 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(71): Show |
74 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.602-22420_602-2241 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0091g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.602-22425_602-2241 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673433 | GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0066g0300 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-22428_602-2241 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | ||||||
chr2:202673444 | T | G | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-22437T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673444 | |||||||
chr2:202673568 | C | G | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-22313C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673568 | |||||||
chr2:202673605 | A | G | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-22276A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673605 | |||||||
chr2:202673608 | C | T | 8 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-22273C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673608 | |||||||
chr2:202673651 | T | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-22230T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673651 | |||||||
chr2:202673784 | T | A | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-22097T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673784 | |||||||
chr2:202673893 | A | T | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-21988A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673893 | |||||||
chr2:202674027 | C | G | 1 | a0001c0001t0079g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.602-21854C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674027 | |||||||
chr2:202674033 | C | G | 26 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(23): Show |
26 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.602-21848C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674033 | |||||||
chr2:202674343 | C | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-21538C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674343 | |||||||
chr2:202674580 | C | T | 1 | a0001c0001t0081g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-21301C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674580 | |||||||
chr2:202674957 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.602-20924G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674957 | |||||||
chr2:202675090 | C | G | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-20791C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675090 | |||||||
chr2:202675101 | G | A | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.602-20780G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675101 | |||||||
chr2:202675180 | A | C | 21 | a0001c0001t0001g0120 a0001c0001t0001g0141 a0001c0001t0001g0152 others(18): Show |
21 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-20701A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675180 | |||||||
chr2:202675237 | A | C | 98 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(95): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.602-20644A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675237 | |||||||
chr2:202675445 | C | CA | 13 | a0001c0001t0001g0253 a0001c0001t0003g0186 a0001c0001t0017g0187 others(10): Show |
13 | HG02027.hp1 HG02451.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.602-20413dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | ||||||
chr2:202675445 | C | CAA | 46 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(43): Show |
46 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.602-20414_602-2041 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | ||||||
chr2:202675445 | C | CAAA | 159 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(156): Show |
159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.602-20415_602-2041 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | ||||||
chr2:202675445 | C | CAAAA | 28 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0147 others(25): Show |
28 | HG00597.hp1 HG00642.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.602-20416_602-2041 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | ||||||
chr2:202675526 | C | T | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-20355C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675526 | |||||||
chr2:202675547 | T | C | 1 | a0001c0001t0080g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602-20334T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675547 | |||||||
chr2:202675630 | G | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-20251G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675630 | |||||||
chr2:202675712 | T | C | 247 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(244): Show |
247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.602-20169T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675712 | |||||||
chr2:202675733 | C | G | 3 | a0001c0001t0013g0132 a0001c0001t0048g0129 a0001c0001t0048g0130 |
3 | HG02071.hp1 NA18970.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.602-20148C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675733 | |||||||
chr2:202675737 | A | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-20144A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675737 | |||||||
chr2:202675741 | C | T | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-20140C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675741 | |||||||
chr2:202675940 | G | A | 1 | a0001c0001t0081g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-19941G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675940 | |||||||
chr2:202675984 | C | CA | 17 | a0001c0001t0001g0060 a0001c0001t0001g0172 a0001c0001t0002g0097 others(14): Show |
17 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.602-19876dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | ||||||
chr2:202675984 | C | CAA | 27 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(24): Show |
27 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-19877_602-1987 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | ||||||
chr2:202675984 | CA | C | 13 | a0001c0001t0005g0051 a0001c0001t0007g0057 a0001c0001t0008g0189 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.602-19876delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | ||||||
chr2:202676109 | A | G | 28 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(25): Show |
28 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-19772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676109 | |||||||
chr2:202676180 | A | G | 1 | a0001c0001t0042g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.602-19701A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676180 | |||||||
chr2:202676375 | GT | G | 222 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(219): Show |
222 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.602-19490delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202676375 | ||||||
chr2:202676441 | G | A | 1 | a0001c0001t0003g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.602-19440G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676441 | |||||||
chr2:202676831 | C | T | 2 | a0001c0001t0008g0049 a0001c0001t0017g0050 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.602-19050C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676831 | |||||||
chr2:202676931 | T | C | 70 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(67): Show |
70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-18950T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676931 | |||||||
chr2:202676946 | G | T | 20 | a0001c0001t0002g0054 a0001c0001t0002g0081 a0001c0001t0002g0092 others(17): Show |
20 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.602-18935G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676946 | |||||||
chr2:202677027 | T | C | 98 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(95): Show |
98 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.602-18854T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677027 | |||||||
chr2:202677063 | C | CT | 30 | a0001c0001t0007g0066 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-18803dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202677063 | ||||||
chr2:202677073 | T | G | 3 | a0001c0001t0025g0259 a0001c0001t0025g0261 a0001c0001t0086g0265 |
3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.602-18808T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677073 | |||||||
chr2:202677093 | C | T | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-18788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677093 | |||||||
chr2:202677163 | G | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18718G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677163 | |||||||
chr2:202677192 | C | T | 2 | a0001c0001t0008g0226 a0001c0001t0047g0225 |
2 | HG01952.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.602-18689C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677192 | |||||||
chr2:202677302 | G | A | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-18579G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677302 | |||||||
chr2:202677308 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18573C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677308 | |||||||
chr2:202677433 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.602-18448G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677433 | |||||||
chr2:202677533 | G | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18348G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677533 | |||||||
chr2:202677566 | C | T | 1 | a0001c0001t0122g0009 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.602-18315C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677566 | |||||||
chr2:202677781 | A | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18100A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677781 | |||||||
chr2:202677862 | A | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18019A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677862 | |||||||
chr2:202678009 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.602-17872T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678009 | |||||||
chr2:202678139 | A | G | 3 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0003c0003t0010g0103 |
3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.602-17742A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678139 | |||||||
chr2:202678472 | C | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-17409C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678472 | |||||||
chr2:202678581 | C | T | 1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.602-17300C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678581 | |||||||
chr2:202678746 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-17135C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678746 | |||||||
chr2:202678767 | A | C | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.602-17114A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678767 | |||||||
chr2:202679029 | C | G | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-16852C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679029 | |||||||
chr2:202679151 | A | G | 12 | a0001c0001t0005g0051 a0001c0001t0005g0234 a0001c0001t0005g0238 others(9): Show |
12 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-16730A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679151 | |||||||
chr2:202679406 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-16475G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679406 | |||||||
chr2:202679479 | T | C | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-16402T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679479 | |||||||
chr2:202679627 | G | A | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-16254G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679627 | |||||||
chr2:202679723 | A | T | 1 | a0001c0001t0095g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-16158A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679723 | |||||||
chr2:202680010 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-15871G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680010 | |||||||
chr2:202680221 | C | T | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-15660C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680221 | |||||||
chr2:202680266 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.602-15615A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680266 | |||||||
chr2:202680271 | G | T | 1 | a0001c0001t0003g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.602-15610G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680271 | |||||||
chr2:202680286 | G | T | 1 | a0001c0001t0005g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.602-15595G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680286 | |||||||
chr2:202680404 | A | T | 25 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(22): Show |
25 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.602-15477A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680404 | |||||||
chr2:202680421 | T | A | 229 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.602-15460T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680421 | |||||||
chr2:202680475 | C | T | 148 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.602-15406C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680475 | |||||||
chr2:202680543 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-15338C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680543 | |||||||
chr2:202680608 | C | T | 1 | a0001c0001t0095g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-15273C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680608 | |||||||
chr2:202680642 | A | G | 1 | a0001c0001t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.602-15239A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680642 | |||||||
chr2:202681021 | T | C | 1 | a0001c0001t0094g0230 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.602-14860T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681021 | |||||||
chr2:202681476 | C | T | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-14405C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681476 | |||||||
chr2:202681531 | A | G | 9 | a0001c0001t0005g0234 a0001c0001t0005g0238 a0001c0001t0008g0049 others(6): Show |
9 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-14350A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681531 | |||||||
chr2:202681586 | T | A | 3 | a0002c0002t0021g0290 a0002c0002t0021g0291 a0002c0002t0073g0292 |
3 | HG03130.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.602-14295T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681586 | |||||||
chr2:202681814 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0009g0084 a0001c0001t0031g0083 |
3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-14067C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681814 | |||||||
chr2:202681980 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.602-13901G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681980 | |||||||
chr2:202682027 | T | C | 1 | a0001c0001t0009g0010 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-13854T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682027 | |||||||
chr2:202682037 | C | T | 8 | a0001c0001t0005g0118 a0001c0001t0028g0161 a0001c0001t0028g0162 others(5): Show |
8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-13844C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682037 | |||||||
chr2:202682050 | C | T | 1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.602-13831C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682050 | |||||||
chr2:202682150 | C | T | 78 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(75): Show |
78 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.602-13731C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682150 | |||||||
chr2:202682166 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0009g0084 a0001c0001t0031g0083 |
3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-13715C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682166 | |||||||
chr2:202682383 | C | T | 25 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(22): Show |
25 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.602-13498C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682383 | |||||||
chr2:202682739 | G | A | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.602-13142G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682739 | |||||||
chr2:202682890 | G | T | 1 | a0001c0001t0009g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-12991G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682890 | |||||||
chr2:202682902 | TATA | T | 6 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0009g0256 others(3): Show |
6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-12977_602-1297 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202682902 | ||||||
chr2:202683093 | C | T | 26 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(23): Show |
26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.602-12788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683093 | |||||||
chr2:202683098 | C | T | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-12783C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683098 | |||||||
chr2:202683114 | G | C | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-12767G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683114 | |||||||
chr2:202683147 | G | A | 1 | a0001c0001t0008g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.602-12734G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683147 | |||||||
chr2:202683164 | C | G | 6 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-12717C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683164 | |||||||
chr2:202683184 | C | T | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.602-12697C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683184 | |||||||
chr2:202683198 | T | C | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-12683T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683198 | |||||||
chr2:202683278 | G | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-12603G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683278 | |||||||
chr2:202683336 | CAAAA | C | 21 | a0001c0001t0001g0120 a0001c0001t0001g0141 a0001c0001t0001g0152 others(18): Show |
21 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-12542_602-1253 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202683336 | ||||||
chr2:202683612 | C | A | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-12269C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683612 | |||||||
chr2:202683630 | T | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-12251T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683630 | |||||||
chr2:202683696 | C | G | 1 | a0001c0001t0003g0042 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.602-12185C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683696 | |||||||
chr2:202683812 | T | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-12069T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683812 | |||||||
chr2:202683929 | C | T | 1 | a0001c0001t0011g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.602-11952C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683929 | |||||||
chr2:202684015 | C | T | 1 | a0001c0001t0055g0282 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.602-11866C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684015 | |||||||
chr2:202684087 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.602-11794G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684087 | |||||||
chr2:202684288 | A | G | 260 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(257): Show |
260 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.602-11593A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684288 | |||||||
chr2:202684302 | CTTA | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-11573_602-1157 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684302 | ||||||
chr2:202684328 | C | T | 2 | a0001c0001t0014g0059 a0001c0001t0046g0168 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.602-11553C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684328 | |||||||
chr2:202684363 | C | T | 1 | a0001c0004t0038g0013 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.602-11518C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684363 | |||||||
chr2:202684437 | T | C | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-11444T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684437 | |||||||
chr2:202684465 | C | T | 3 | a0001c0001t0025g0259 a0001c0001t0025g0261 a0001c0001t0086g0265 |
3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.602-11416C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684465 | |||||||
chr2:202684492 | G | A | 1 | a0001c0001t0017g0050 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.602-11389G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684492 | |||||||
chr2:202684494 | G | A | 34 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-11387G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684494 | |||||||
chr2:202684521 | C | T | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.602-11360C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684521 | |||||||
chr2:202684663 | G | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-11218G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684663 | |||||||
chr2:202684685 | T | TTA | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-11193_602-1119 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684685 | ||||||
chr2:202684879 | T | C | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.602-11002T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684879 | |||||||
chr2:202684917 | A | C | 1 | a0001c0001t0013g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.602-10964A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684917 | |||||||
chr2:202684990 | A | AT | 14 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(11): Show |
14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.602-10879dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684990 | ||||||
chr2:202684990 | A | T | 6 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0009g0256 others(3): Show |
6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-10891A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684990 | |||||||
chr2:202684991 | T | A | 5 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-10890T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684991 | |||||||
chr2:202685017 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.602-10864C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685017 | |||||||
chr2:202685149 | A | T | 1 | a0001c0001t0013g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.602-10732A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685149 | |||||||
chr2:202685234 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-10647C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685234 | |||||||
chr2:202685302 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.602-10579C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685302 | |||||||
chr2:202685475 | G | A | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10406G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685475 | |||||||
chr2:202685658 | A | G | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-10223A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685658 | |||||||
chr2:202685751 | C | T | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10130C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685751 | |||||||
chr2:202685779 | A | C | 29 | a0002c0002t0006g0302 a0002c0002t0006g0305 a0002c0002t0006g0306 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10102A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685779 | |||||||
chr2:202685847 | G | A | 1 | a0001c0001t0049g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.602-10034G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685847 | |||||||
chr2:202686018 | T | C | 155 | a0001c0001t0001g0017 a0001c0001t0001g0253 a0001c0001t0001g0255 others(152): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.602-9863T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686018 | |||||||
chr2:202686049 | C | A | 6 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-9832C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686049 | |||||||
chr2:202686100 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.602-9781A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686100 | |||||||
chr2:202686117 | T | G | 1 | a0001c0001t0020g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.602-9764T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686117 | |||||||
chr2:202686163 | T | C | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-9718T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686163 | |||||||
chr2:202686584 | G | A | 1 | a0001c0001t0097g0039 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.602-9297G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686584 | |||||||
chr2:202686637 | C | T | 2 | a0002c0002t0016g0299 a0002c0002t0070g0295 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602-9244C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686637 | |||||||
chr2:202686805 | C | CA | 71 | a0001c0001t0001g0017 a0001c0001t0001g0172 a0001c0001t0002g0054 others(68): Show |
71 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.602-9063dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202686805 | ||||||
chr2:202686822 | G | T | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.602-9059G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686822 | |||||||
chr2:202686825 | T | C | 1 | a0001c0001t0090g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.602-9056T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686825 | |||||||
chr2:202686869 | G | A | 1 | a0001c0001t0118g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.602-9012G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686869 | |||||||
chr2:202686899 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602-8982A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686899 | |||||||
chr2:202687149 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-8732A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687149 | |||||||
chr2:202687375 | A | G | 1 | a0002c0005t0016g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.602-8506A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687375 | |||||||
chr2:202687617 | C | T | 1 | a0001c0001t0122g0009 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.602-8264C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687617 | |||||||
chr2:202687618 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.602-8263C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687618 | |||||||
chr2:202687684 | T | G | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.602-8197T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687684 | |||||||
chr2:202687687 | A | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-8194A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687687 | |||||||
chr2:202687710 | C | G | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.602-8171C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687710 | |||||||
chr2:202687820 | T | C | 1 | a0001c0001t0089g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.602-8061T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687820 | |||||||
chr2:202687860 | G | T | 1 | a0001c0001t0099g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.602-8021G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687860 | |||||||
chr2:202688469 | T | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0220 a0001c0001t0003g0149 others(3): Show |
6 | HG02155.hp2 NA18940.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-7412T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688469 | |||||||
chr2:202688531 | T | G | 1 | a0002c0002t0069g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.602-7350T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688531 | |||||||
chr2:202688652 | T | G | 1 | a0001c0001t0022g0201 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.602-7229T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688652 | |||||||
chr2:202688904 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-6977C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688904 | |||||||
chr2:202689113 | G | A | 78 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(75): Show |
78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.602-6768G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689113 | |||||||
chr2:202689191 | A | C | 1 | a0001c0001t0009g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-6690A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689191 | |||||||
chr2:202689601 | A | C | 16 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(13): Show |
16 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-6280A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689601 | |||||||
chr2:202689911 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0009g0084 a0001c0001t0031g0083 |
3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-5970C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689911 | |||||||
chr2:202689912 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-5969G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689912 | |||||||
chr2:202690484 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-5397C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690484 | |||||||
chr2:202690620 | G | T | 175 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(172): Show |
175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.602-5261G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690620 | |||||||
chr2:202690796 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.602-5085A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690796 | |||||||
chr2:202690981 | CT | C | 33 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(30): Show |
33 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.602-4895delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202690981 | ||||||
chr2:202691043 | A | C | 1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.602-4838A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691043 | |||||||
chr2:202691105 | C | T | 63 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0186 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.602-4776C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691105 | |||||||
chr2:202691452 | T | A | 1 | a0001c0001t0081g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-4429T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691452 | |||||||
chr2:202691501 | T | TA | 13 | a0001c0001t0005g0207 a0001c0001t0036g0286 a0001c0001t0036g0287 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-4369dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691501 | ||||||
chr2:202691501 | TA | T | 175 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(172): Show |
175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.602-4369delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691501 | ||||||
chr2:202691503 | A | T | 5 | a0001c0001t0002g0074 a0001c0001t0002g0088 a0001c0001t0023g0086 others(2): Show |
5 | HG00099.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4378A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691503 | |||||||
chr2:202691581 | A | G | 1 | a0001c0001t0049g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.602-4300A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691581 | |||||||
chr2:202691581 | ATAGT | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4296_602-4293d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691581 | ||||||
chr2:202691649 | T | TTG | 4 | a0001c0001t0049g0209 a0001c0001t0083g0102 a0002c0002t0021g0291 others(1): Show |
4 | HG03225.hp1 HG03516.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-4183_602-4182d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | T | TTGTG | 5 | a0001c0001t0008g0227 a0001c0001t0034g0185 a0001c0001t0047g0225 others(2): Show |
5 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4185_602-4182d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0020g0030 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.602-4217_602-4216i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTG | T | 43 | a0001c0001t0001g0120 a0001c0001t0001g0163 a0001c0001t0001g0253 others(40): Show |
43 | HG00408.hp1 HG01109.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.602-4183_602-4182d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTGTG | T | 50 | a0001c0001t0001g0061 a0001c0001t0001g0156 a0001c0001t0001g0255 others(47): Show |
50 | HG00099.hp1 HG00544.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.602-4185_602-4182d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTGTGTG | T | 61 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(58): Show |
61 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.602-4187_602-4182d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTGTGTGT others(1): Show |
T | 26 | a0001c0001t0001g0123 a0001c0001t0001g0136 a0001c0001t0001g0196 others(23): Show |
26 | HG00140.hp1 HG01346.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.602-4189_602-4182d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0114 a0001c0001t0003g0149 a0001c0001t0014g0219 others(2): Show |
5 | HG02818.hp2 NA18988.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4191_602-4182d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691649 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0089g0016 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.602-4195_602-4182d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | ||||||
chr2:202691651 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.602-4217_602-4216i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691651 | ||||||
chr2:202691653 | G | GTGTGTGT others(5): Show |
2 | a0001c0001t0019g0033 a0001c0001t0020g0032 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.602-4217_602-4216i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691653 | ||||||
chr2:202691655 | G | GTGTGTGT others(3): Show |
7 | a0001c0001t0004g0022 a0001c0001t0004g0028 a0001c0001t0004g0031 others(4): Show |
7 | HG00140.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691655 | ||||||
chr2:202691657 | G | GTGTGTGT others(1): Show |
4 | a0001c0001t0004g0027 a0001c0001t0004g0029 a0001c0001t0019g0036 others(1): Show |
4 | HG00639.hp1 HG01261.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691657 | ||||||
chr2:202691657 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.602-4215_602-4214i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691657 | ||||||
chr2:202691659 | G | GTGTGTA | 3 | a0001c0001t0004g0100 a0001c0001t0119g0023 a0001c0001t0122g0009 |
3 | HG00544.hp2 HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.602-4217_602-4216i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691659 | ||||||
chr2:202691663 | G | GTA | 5 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(2): Show |
5 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691663 | ||||||
chr2:202691667 | G | A | 1 | a0001c0001t0117g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.602-4214G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691667 | |||||||
chr2:202691682 | TGTGTGTG others(11): Show |
T | 1 | a0002c0002t0059g0316 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.602-4197_602-4180d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691682 | ||||||
chr2:202691690 | TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.602-4189_602-4180d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691690 | ||||||
chr2:202691692 | TGTGTGTG others(1): Show |
T | 5 | a0001c0001t0008g0004 a0001c0001t0028g0002 a0001c0001t0036g0286 others(2): Show |
5 | HG02622.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4187_602-4180d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691692 | ||||||
chr2:202691694 | T | C | 1 | a0001c0001t0009g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-4187T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691694 | |||||||
chr2:202691696 | T | C | 15 | a0001c0001t0002g0058 a0001c0001t0002g0071 a0001c0001t0002g0073 others(12): Show |
15 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.602-4185T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691696 | |||||||
chr2:202691696 | T | TGC | 7 | a0001c0001t0002g0068 a0001c0001t0002g0098 a0001c0001t0007g0014 others(4): Show |
7 | HG00408.hp2 HG01361.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-4184_602-4183i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691696 | ||||||
chr2:202691696 | TGTGC | T | 3 | a0001c0001t0005g0003 a0001c0007t0068g0285 a0002c0002t0060g0317 |
3 | HG02257.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.602-4183_602-4180d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691696 | ||||||
chr2:202691698 | T | C | 134 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(131): Show |
134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.602-4183T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691698 | |||||||
chr2:202691698 | T | TGC | 15 | a0001c0001t0001g0147 a0001c0001t0001g0241 a0001c0001t0002g0074 others(12): Show |
15 | HG00642.hp2 HG01071.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-4174_602-4173d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | ||||||
chr2:202691698 | T | TGTGC | 12 | a0001c0001t0001g0176 a0001c0001t0002g0088 a0001c0001t0015g0271 others(9): Show |
12 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-4182_602-4181i others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | ||||||
chr2:202691698 | T | TGTGTGCG others(3): Show |
1 | a0001c0001t0007g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.602-4182_602-4181i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | ||||||
chr2:202691698 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0009g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-4182_602-4181i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | ||||||
chr2:202691700 | C | T | 2 | a0001c0001t0008g0221 a0001c0001t0083g0102 |
2 | HG03225.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.602-4181C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691700 | |||||||
chr2:202691744 | G | A | 6 | a0001c0001t0004g0045 a0001c0001t0004g0228 a0001c0001t0115g0048 others(3): Show |
6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-4137G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691744 | |||||||
chr2:202691803 | T | C | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-4078T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691803 | |||||||
chr2:202692149 | A | C | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-3732A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692149 | |||||||
chr2:202692277 | A | G | 1 | a0001c0001t0047g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.602-3604A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692277 | |||||||
chr2:202692428 | T | C | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(25): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-3453T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692428 | |||||||
chr2:202692716 | C | T | 1 | a0001c0001t0039g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.602-3165C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692716 | |||||||
chr2:202692746 | G | A | 8 | a0003c0003t0012g0062 a0003c0003t0012g0246 a0003c0003t0012g0247 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-3135G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692746 | |||||||
chr2:202692785 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0105 others(3): Show |
6 | HG00323.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-3096A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692785 | |||||||
chr2:202692887 | G | C | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.602-2994G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692887 | |||||||
chr2:202692963 | A | C | 2 | a0001c0001t0026g0251 a0001c0001t0026g0252 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.602-2918A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692963 | |||||||
chr2:202693196 | G | A | 1 | a0001c0001t0011g0095 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.602-2685G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693196 | |||||||
chr2:202693334 | T | TGTG | 34 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-2543_602-2541d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202693334 | ||||||
chr2:202693442 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-2439C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693442 | |||||||
chr2:202693582 | C | T | 1 | a0001c0001t0049g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.602-2299C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693582 | |||||||
chr2:202693596 | AAAAAC | A | 3 | a0001c0001t0022g0110 a0001c0001t0022g0194 a0001c0001t0078g0096 |
3 | HG02155.hp1 NA18747.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.602-2271_602-2267d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202693596 | ||||||
chr2:202693718 | G | C | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-2163G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693718 | |||||||
chr2:202693800 | G | A | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-2081G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693800 | |||||||
chr2:202693808 | A | G | 69 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.602-2073A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693808 | |||||||
chr2:202694177 | A | C | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-1704A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694177 | |||||||
chr2:202694188 | C | CT | 39 | a0001c0001t0001g0141 a0001c0001t0003g0042 a0001c0001t0004g0019 others(36): Show |
39 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-1672dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0008g0004 a0001c0001t0047g0006 |
2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.602-1681_602-1672d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-1682_602-1672d others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-1683_602-1672d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(6): Show |
1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.602-1684_602-1672d others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0064g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.602-1685_602-1672d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(11): Show |
2 | a0002c0002t0016g0299 a0002c0002t0070g0295 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602-1689_602-1672d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(12): Show |
5 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0067g0315 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-1690_602-1672d others(21): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0066g0300 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-1691_602-1672d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694188 | CTTTTTT | C | 15 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-1677_602-1672d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | ||||||
chr2:202694282 | T | C | 250 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(247): Show |
250 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.602-1599T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694282 | |||||||
chr2:202694387 | C | T | 1 | a0001c0001t0009g0010 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-1494C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694387 | |||||||
chr2:202694506 | A | G | 2 | a0001c0001t0095g0199 a0001c0001t0100g0204 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.602-1375A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694506 | |||||||
chr2:202694528 | C | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-1353C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694528 | |||||||
chr2:202694627 | G | A | 1 | a0001c0001t0094g0230 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.602-1254G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694627 | |||||||
chr2:202694718 | G | C | 34 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(31): Show |
34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-1163G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694718 | |||||||
chr2:202694721 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.602-1160C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694721 | |||||||
chr2:202694837 | A | T | 1 | a0001c0001t0007g0066 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.602-1044A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694837 | |||||||
chr2:202695055 | G | A | 15 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(12): Show |
15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-826G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695055 | |||||||
chr2:202695416 | C | G | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-465C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695416 | |||||||
chr2:202695489 | C | A | 1 | a0001c0001t0009g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-392C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695489 | |||||||
chr2:202695510 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.602-371T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695510 | |||||||
chr2:202696062 | T | G | 1 | a0001c0001t0029g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.753+30T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696062 | |||||||
chr2:202696353 | C | T | 29 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(26): Show |
29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.753+321C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696353 | |||||||
chr2:202696507 | C | T | 3 | a0001c0001t0017g0040 a0001c0001t0051g0111 a0001c0001t0051g0179 |
3 | HG00140.hp1 HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.753+475C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696507 | |||||||
chr2:202696592 | G | C | 1 | a0001c0001t0080g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.753+560G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696592 | |||||||
chr2:202696811 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.753+779G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696811 | |||||||
chr2:202696832 | G | A | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+800G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696832 | |||||||
chr2:202697099 | A | G | 2 | a0001c0001t0011g0067 a0001c0001t0011g0078 |
2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.753+1067A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697099 | |||||||
chr2:202697532 | A | T | 1 | a0001c0001t0032g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.753+1500A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697532 | |||||||
chr2:202697562 | T | C | 4 | a0001c0001t0015g0271 a0001c0001t0052g0274 a0001c0001t0053g0273 others(1): Show |
4 | NA18939.hp2 NA18974.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+1530T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697562 | |||||||
chr2:202697573 | T | G | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+1541T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697573 | |||||||
chr2:202697590 | G | A | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+1558G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697590 | |||||||
chr2:202697694 | C | T | 1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.753+1662C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697694 | |||||||
chr2:202698000 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.753+1968G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698000 | |||||||
chr2:202698017 | A | G | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.753+1985A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698017 | |||||||
chr2:202698144 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.753+2112C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698144 | |||||||
chr2:202698323 | G | A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+2291G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698323 | |||||||
chr2:202698384 | C | T | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753+2352C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698384 | |||||||
chr2:202698549 | A | G | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+2517A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698549 | |||||||
chr2:202698571 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0054g0272 |
2 | NA18999.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.753+2539C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698571 | |||||||
chr2:202698572 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0045g0171 a0001c0001t0046g0121 |
3 | NA18940.hp1 NA18977.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.753+2540G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698572 | |||||||
chr2:202698665 | C | T | 2 | a0001c0004t0038g0012 a0001c0004t0038g0013 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.753+2633C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698665 | |||||||
chr2:202698669 | C | T | 4 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+2637C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698669 | |||||||
chr2:202698713 | G | A | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+2681G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698713 | |||||||
chr2:202698778 | C | G | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.753+2746C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698778 | |||||||
chr2:202699369 | G | A | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3337G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699369 | |||||||
chr2:202699426 | C | CA | 12 | a0001c0001t0001g0163 a0001c0001t0003g0186 a0001c0001t0004g0100 others(9): Show |
12 | HG01192.hp1 HG01358.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+3416dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699426 | ||||||
chr2:202699426 | CA | C | 9 | a0001c0001t0001g0123 a0001c0001t0010g0018 a0001c0001t0010g0254 others(6): Show |
9 | HG01168.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+3416delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699426 | ||||||
chr2:202699445 | A | G | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.753+3413A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699445 | |||||||
chr2:202699449 | G | A | 14 | a0001c0001t0002g0097 a0001c0001t0005g0003 a0001c0001t0008g0004 others(11): Show |
14 | HG00621.hp1 HG01109.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.753+3417G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699449 | |||||||
chr2:202699449 | GA | G | 98 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(95): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.753+3432delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699449 | ||||||
chr2:202699449 | GAA | G | 7 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(4): Show |
7 | HG01884.hp2 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+3431_753+3432d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699449 | ||||||
chr2:202699450 | A | AG | 8 | a0001c0001t0028g0002 a0001c0001t0036g0286 a0001c0001t0036g0287 others(5): Show |
8 | HG02109.hp1 HG02723.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+3418_753+3419i others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699450 | |||||||
chr2:202699450 | A | G | 7 | a0001c0001t0002g0097 a0001c0001t0005g0003 a0001c0001t0008g0004 others(4): Show |
7 | HG00621.hp1 HG01109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+3418A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699450 | |||||||
chr2:202699580 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.753+3548C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699580 | |||||||
chr2:202699604 | A | T | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3572A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699604 | |||||||
chr2:202699752 | C | A | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3720C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699752 | |||||||
chr2:202699959 | C | A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+3927C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699959 | |||||||
chr2:202700001 | G | T | 1 | a0001c0001t0117g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.753+3969G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700001 | |||||||
chr2:202700276 | CAGCT | C | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+4248_753+4251d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202700276 | ||||||
chr2:202700399 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.753+4367G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700399 | |||||||
chr2:202700685 | A | AT | 58 | a0001c0001t0002g0093 a0001c0001t0005g0003 a0001c0001t0005g0118 others(55): Show |
58 | HG00733.hp1 HG01109.hp2 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.753+4672dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202700685 | ||||||
chr2:202700713 | G | A | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+4681G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700713 | |||||||
chr2:202700761 | G | A | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+4729G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700761 | |||||||
chr2:202701106 | T | C | 1 | a0003c0003t0010g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.753+5074T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701106 | |||||||
chr2:202701254 | T | C | 2 | a0001c0001t0015g0275 a0001c0001t0056g0280 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.753+5222T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701254 | |||||||
chr2:202701355 | C | A | 18 | a0001c0001t0001g0106 a0001c0001t0001g0146 a0001c0001t0001g0147 others(15): Show |
18 | HG00642.hp2 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.753+5323C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701355 | |||||||
chr2:202701582 | T | C | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.753+5550T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701582 | |||||||
chr2:202701634 | C | G | 1 | a0001c0001t0106g0212 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.753+5602C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701634 | |||||||
chr2:202701753 | G | A | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.753+5721G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701753 | |||||||
chr2:202701998 | A | G | 9 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(6): Show |
9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+5966A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701998 | |||||||
chr2:202702001 | G | C | 76 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.753+5969G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702001 | |||||||
chr2:202702055 | G | T | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+6023G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702055 | |||||||
chr2:202702114 | C | T | 2 | a0003c0003t0012g0062 a0003c0003t0012g0248 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.753+6082C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702114 | |||||||
chr2:202702121 | G | A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+6089G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702121 | |||||||
chr2:202702198 | C | T | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+6166C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702198 | |||||||
chr2:202702227 | T | C | 40 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(37): Show |
40 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.753+6195T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702227 | |||||||
chr2:202702242 | T | G | 1 | a0001c0001t0005g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.753+6210T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702242 | |||||||
chr2:202702288 | G | T | 1 | a0001c0001t0005g0122 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.753+6256G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702288 | |||||||
chr2:202702313 | C | T | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+6281C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702313 | |||||||
chr2:202702414 | T | G | 12 | a0001c0001t0008g0227 a0001c0001t0025g0213 a0001c0001t0025g0259 others(9): Show |
12 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+6382T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702414 | |||||||
chr2:202702703 | G | A | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.753+6671G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702703 | |||||||
chr2:202702743 | C | T | 2 | a0003c0003t0012g0062 a0003c0003t0012g0248 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.753+6711C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702743 | |||||||
chr2:202702775 | G | A | 1 | a0001c0001t0047g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.753+6743G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702775 | |||||||
chr2:202702821 | G | A | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+6789G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702821 | |||||||
chr2:202702956 | A | G | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.753+6924A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702956 | |||||||
chr2:202703219 | A | G | 2 | a0002c0002t0037g0293 a0002c0002t0037g0311 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.753+7187A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703219 | |||||||
chr2:202703225 | C | G | 2 | a0001c0001t0107g0266 a0002c0002t0067g0315 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.753+7193C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703225 | |||||||
chr2:202703359 | A | G | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+7327A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703359 | |||||||
chr2:202703468 | G | T | 1 | a0001c0001t0079g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.753+7436G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703468 | |||||||
chr2:202703510 | A | ATG | 5 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+7479_753+7480d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202703510 | ||||||
chr2:202704235 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.753+8203T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704235 | |||||||
chr2:202704237 | T | C | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.753+8205T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704237 | |||||||
chr2:202704365 | A | G | 3 | a0001c0001t0001g0253 a0001c0001t0026g0251 a0001c0001t0026g0252 |
3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.753+8333A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704365 | |||||||
chr2:202704564 | T | C | 19 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(16): Show |
19 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.753+8532T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704564 | |||||||
chr2:202704626 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.753+8594A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704626 | |||||||
chr2:202704788 | A | G | 3 | a0001c0001t0002g0071 a0001c0001t0003g0070 a0001c0001t0043g0069 |
3 | HG02165.hp2 NA18954.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.753+8756A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704788 | |||||||
chr2:202704843 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.753+8811C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704843 | |||||||
chr2:202704907 | T | A | 3 | a0002c0002t0016g0297 a0002c0002t0071g0301 a0002c0005t0016g0298 |
3 | HG02615.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.753+8875T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704907 | |||||||
chr2:202705165 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+9133G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705165 | |||||||
chr2:202705174 | C | T | 1 | a0001c0001t0015g0271 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.753+9142C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705174 | |||||||
chr2:202705175 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0097 |
2 | HG00621.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.753+9143G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705175 | |||||||
chr2:202705293 | T | TGAAA | 7 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(4): Show |
7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+9262_753+9265d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202705293 | ||||||
chr2:202705537 | C | CTGAG | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+9506_753+9509d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202705537 | ||||||
chr2:202705719 | C | T | 1 | a0001c0001t0029g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.753+9687C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705719 | |||||||
chr2:202705764 | A | G | 249 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(246): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.753+9732A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705764 | |||||||
chr2:202705848 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+9816G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705848 | |||||||
chr2:202706038 | G | C | 26 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(23): Show |
26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.753+10006G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706038 | |||||||
chr2:202706082 | G | A | 1 | a0001c0001t0013g0008 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.753+10050G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706082 | |||||||
chr2:202706098 | A | T | 1 | a0001c0001t0005g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.753+10066A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706098 | |||||||
chr2:202706170 | C | T | 1 | a0001c0001t0029g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.753+10138C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706170 | |||||||
chr2:202706456 | A | G | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.753+10424A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706456 | |||||||
chr2:202706530 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0003g0089 a0001c0001t0014g0108 |
3 | NA18948.hp2 NA18964.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.753+10498G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706530 | |||||||
chr2:202706724 | T | C | 1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.753+10692T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706724 | |||||||
chr2:202706772 | G | A | 16 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.753+10740G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706772 | |||||||
chr2:202706848 | G | A | 2 | a0001c0001t0015g0275 a0001c0001t0056g0280 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.753+10816G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706848 | |||||||
chr2:202706919 | C | T | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+10887C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706919 | |||||||
chr2:202706928 | TGA | T | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+10899_753+1090 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202706928 | ||||||
chr2:202707017 | G | C | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+10985G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707017 | |||||||
chr2:202707100 | G | T | 4 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+11068G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707100 | |||||||
chr2:202707215 | AT | A | 75 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(72): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.753+11197delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202707215 | ||||||
chr2:202707230 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.753+11198G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707230 | |||||||
chr2:202707236 | A | G | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.753+11204A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707236 | |||||||
chr2:202707239 | C | G | 259 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(256): Show |
259 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.753+11207C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707239 | |||||||
chr2:202707364 | G | A | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.753+11332G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707364 | |||||||
chr2:202707471 | C | T | 2 | a0001c0001t0011g0067 a0001c0001t0011g0078 |
2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.753+11439C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707471 | |||||||
chr2:202707484 | A | C | 2 | a0001c0001t0008g0049 a0001c0001t0017g0050 |
2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.753+11452A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707484 | |||||||
chr2:202707672 | A | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+11640A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707672 | |||||||
chr2:202707772 | AT | A | 41 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0013g0008 others(38): Show |
41 | HG00609.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.753+11754delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202707772 | ||||||
chr2:202708119 | C | T | 35 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(32): Show |
35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.753+12087C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708119 | |||||||
chr2:202708239 | A | G | 1 | a0003c0003t0112g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.753+12207A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708239 | |||||||
chr2:202708264 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.753+12232T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708264 | |||||||
chr2:202708432 | T | A | 66 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(63): Show |
66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.753+12400T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708432 | |||||||
chr2:202708562 | A | C | 1 | a0001c0001t0008g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.753+12530A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708562 | |||||||
chr2:202708665 | G | A | 75 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(72): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.753+12633G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708665 | |||||||
chr2:202708667 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+12635G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708667 | |||||||
chr2:202708901 | C | T | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+12869C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708901 | |||||||
chr2:202709273 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.753+13241A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709273 | |||||||
chr2:202709902 | C | A | 1 | a0001c0001t0019g0035 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.753+13870C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709902 | |||||||
chr2:202709907 | A | G | 1 | a0001c0001t0011g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.753+13875A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709907 | |||||||
chr2:202710209 | G | T | 1 | a0001c0001t0093g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.753+14177G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710209 | |||||||
chr2:202710383 | A | G | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.753+14351A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710383 | |||||||
chr2:202710424 | A | C | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+14392A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710424 | |||||||
chr2:202710715 | G | A | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.754-14202G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710715 | |||||||
chr2:202710847 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0215 |
2 | HG00621.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.754-14070A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710847 | |||||||
chr2:202711229 | C | T | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-13688C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711229 | |||||||
chr2:202711276 | A | G | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-13641A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711276 | |||||||
chr2:202711857 | G | A | 11 | a0001c0001t0015g0271 a0001c0001t0015g0275 a0001c0001t0015g0276 others(8): Show |
11 | HG00558.hp2 HG02080.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-13060G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711857 | |||||||
chr2:202711927 | A | G | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.754-12990A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711927 | |||||||
chr2:202712166 | A | C | 9 | a0001c0001t0005g0118 a0001c0001t0026g0124 a0001c0001t0028g0161 others(6): Show |
9 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-12751A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712166 | |||||||
chr2:202712199 | T | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-12718T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712199 | |||||||
chr2:202712419 | C | CT | 28 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0005g0003 others(25): Show |
28 | HG00741.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.754-12476dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | ||||||
chr2:202712419 | C | CTT | 17 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(14): Show |
17 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.754-12477_754-1247 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | ||||||
chr2:202712419 | CT | C | 100 | a0001c0001t0001g0017 a0001c0001t0001g0144 a0001c0001t0001g0163 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.754-12476delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | ||||||
chr2:202712445 | C | T | 1 | a0001c0001t0031g0157 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.754-12472C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712445 | |||||||
chr2:202712665 | A | G | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.754-12252A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712665 | |||||||
chr2:202712729 | A | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-12188A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712729 | |||||||
chr2:202713173 | C | T | 1 | a0001c0001t0029g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.754-11744C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713173 | |||||||
chr2:202713285 | A | G | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(25): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.754-11632A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713285 | |||||||
chr2:202713287 | T | C | 3 | a0001c0001t0005g0051 a0001c0001t0035g0278 a0001c0001t0082g0231 |
3 | HG00597.hp2 NA18948.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.754-11630T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713287 | |||||||
chr2:202713305 | C | T | 1 | a0001c0001t0043g0069 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.754-11612C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713305 | |||||||
chr2:202713467 | C | A | 16 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(13): Show |
16 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.754-11450C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713467 | |||||||
chr2:202713583 | C | G | 168 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(165): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.754-11334C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713583 | |||||||
chr2:202713700 | A | T | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-11217A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713700 | |||||||
chr2:202713860 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0014g0131 |
2 | HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.754-11057C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713860 | |||||||
chr2:202713967 | C | T | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10950C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713967 | |||||||
chr2:202714187 | G | C | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-10730G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714187 | |||||||
chr2:202714225 | A | G | 1 | a0001c0001t0045g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.754-10692A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714225 | |||||||
chr2:202714312 | A | G | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.754-10605A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714312 | |||||||
chr2:202714367 | T | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10550T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714367 | |||||||
chr2:202714443 | CTATT | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10471_754-1046 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714443 | ||||||
chr2:202714474 | A | G | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10443A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714474 | |||||||
chr2:202714497 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0217 a0001c0001t0014g0219 |
3 | NA18962.hp1 NA18986.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.754-10420G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714497 | |||||||
chr2:202714520 | ATCTTTTT others(4): Show |
A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10384_754-1037 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714520 | ||||||
chr2:202714522 | CT | C | 38 | a0001c0001t0002g0098 a0001c0001t0005g0003 a0001c0001t0008g0004 others(35): Show |
38 | HG00408.hp2 HG00733.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.754-10385delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714522 | ||||||
chr2:202714527 | T | C | 1 | a0001c0001t0115g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.754-10390T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714527 | |||||||
chr2:202714532 | T | C | 65 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(62): Show |
65 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.754-10385T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714532 | |||||||
chr2:202714533 | C | CT | 36 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(33): Show |
36 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.754-10367dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714533 | ||||||
chr2:202714534 | T | C | 3 | a0001c0001t0002g0098 a0001c0001t0043g0069 a0001c0001t0107g0266 |
3 | HG00408.hp2 HG01884.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.754-10383T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714534 | |||||||
chr2:202714537 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754-10380T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714537 | |||||||
chr2:202714543 | T | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10374T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714543 | |||||||
chr2:202714676 | C | T | 2 | a0001c0001t0009g0010 a0001c0001t0023g0086 |
2 | HG00558.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.754-10241C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714676 | |||||||
chr2:202714899 | C | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10018C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714899 | |||||||
chr2:202715073 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-9844G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715073 | |||||||
chr2:202715135 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.754-9782G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715135 | |||||||
chr2:202715138 | C | T | 15 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(12): Show |
15 | HG01952.hp2 HG02145.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.754-9779C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715138 | |||||||
chr2:202715139 | G | A | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(98): Show |
101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-9778G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715139 | |||||||
chr2:202715143 | C | T | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.754-9774C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715143 | |||||||
chr2:202715182 | G | A | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-9735G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715182 | |||||||
chr2:202715190 | C | T | 4 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0001c0001t0064g0284 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-9727C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715190 | |||||||
chr2:202715229 | G | A | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.754-9688G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715229 | |||||||
chr2:202715250 | G | A | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-9667G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715250 | |||||||
chr2:202715337 | C | T | 1 | a0001c0001t0099g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.754-9580C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715337 | |||||||
chr2:202715347 | C | T | 1 | a0001c0001t0050g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.754-9570C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715347 | |||||||
chr2:202715365 | C | T | 4 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0001c0001t0064g0284 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-9552C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715365 | |||||||
chr2:202715381 | C | T | 1 | a0003c0003t0032g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754-9536C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715381 | |||||||
chr2:202715443 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-9474G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715443 | |||||||
chr2:202715495 | C | T | 1 | a0001c0001t0039g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.754-9422C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715495 | |||||||
chr2:202715527 | G | A | 1 | a0001c0001t0009g0010 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.754-9390G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715527 | |||||||
chr2:202715562 | A | G | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.754-9355A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715562 | |||||||
chr2:202715610 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0101g0174 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.754-9307G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715610 | |||||||
chr2:202715836 | T | C | 1 | a0001c0001t0100g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-9081T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715836 | |||||||
chr2:202715839 | GGAGGCCG others(12): Show |
G | 1 | a0001c0001t0100g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-9077_754-9059d others(21): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715839 | |||||||
chr2:202715854 | C | T | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.754-9063C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715854 | |||||||
chr2:202715889 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.754-9028G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715889 | |||||||
chr2:202715949 | G | A | 2 | a0001c0001t0011g0067 a0001c0001t0011g0078 |
2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.754-8968G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715949 | |||||||
chr2:202715951 | G | A | 1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.754-8966G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715951 | |||||||
chr2:202715961 | A | T | 1 | a0001c0001t0009g0119 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.754-8956A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715961 | |||||||
chr2:202716541 | CTGT | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-8369_754-8367d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202716541 | ||||||
chr2:202716655 | T | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-8262T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716655 | |||||||
chr2:202716722 | C | G | 1 | a0002c0002t0016g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.754-8195C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716722 | |||||||
chr2:202716731 | G | A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-8186G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716731 | |||||||
chr2:202716759 | A | G | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754-8158A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716759 | |||||||
chr2:202717016 | C | T | 1 | a0001c0001t0020g0030 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.754-7901C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717016 | |||||||
chr2:202717017 | G | A | 2 | a0001c0001t0008g0224 a0002c0002t0062g0304 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.754-7900G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717017 | |||||||
chr2:202717086 | A | G | 1 | a0001c0001t0042g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.754-7831A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717086 | |||||||
chr2:202717147 | C | A | 1 | a0002c0005t0016g0298 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.754-7770C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717147 | |||||||
chr2:202717424 | A | G | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754-7493A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717424 | |||||||
chr2:202717466 | T | C | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(98): Show |
101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-7451T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717466 | |||||||
chr2:202717487 | G | A | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-7430G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717487 | |||||||
chr2:202717607 | T | C | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.754-7310T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717607 | |||||||
chr2:202717608 | C | T | 1 | a0001c0001t0009g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.754-7309C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717608 | |||||||
chr2:202717714 | A | C | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.754-7203A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717714 | |||||||
chr2:202717831 | T | TG | 37 | a0001c0001t0032g0007 a0001c0001t0036g0286 a0001c0001t0036g0287 others(34): Show |
37 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.754-7083dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202717831 | ||||||
chr2:202718012 | A | T | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-6905A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718012 | |||||||
chr2:202718124 | G | C | 1 | a0001c0001t0045g0171 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.754-6793G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718124 | |||||||
chr2:202718152 | G | A | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.754-6765G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718152 | |||||||
chr2:202718159 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-6758G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718159 | |||||||
chr2:202718192 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.754-6725T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718192 | |||||||
chr2:202718476 | A | AT | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-6437dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202718476 | ||||||
chr2:202718531 | G | A | 143 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(140): Show |
143 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.754-6386G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718531 | |||||||
chr2:202718578 | A | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-6339A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718578 | |||||||
chr2:202718673 | T | G | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.754-6244T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718673 | |||||||
chr2:202719319 | G | A | 1 | a0001c0004t0076g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.754-5598G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719319 | |||||||
chr2:202719391 | TTTTTA | T | 80 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(77): Show |
80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-5521_754-5517d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202719391 | ||||||
chr2:202719478 | A | G | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-5439A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719478 | |||||||
chr2:202719542 | G | A | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-5375G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719542 | |||||||
chr2:202719733 | G | A | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-5184G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719733 | |||||||
chr2:202719782 | C | G | 3 | a0001c0001t0001g0253 a0001c0001t0026g0251 a0001c0001t0026g0252 |
3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.754-5135C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719782 | |||||||
chr2:202720014 | T | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-4903T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720014 | |||||||
chr2:202720225 | A | G | 67 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.754-4692A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720225 | |||||||
chr2:202720241 | T | C | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.754-4676T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720241 | |||||||
chr2:202720400 | C | CGT | 28 | a0001c0001t0001g0146 a0001c0001t0001g0217 a0001c0001t0009g0010 others(25): Show |
28 | HG00558.hp1 HG00733.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.754-4491_754-4490d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720400 | ||||||
chr2:202720400 | CGTGT | C | 3 | a0001c0001t0001g0253 a0001c0001t0026g0251 a0001c0001t0026g0252 |
3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.754-4493_754-4490d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720400 | ||||||
chr2:202720426 | TGC | T | 36 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(33): Show |
36 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.754-4488_754-4487d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720426 | ||||||
chr2:202720428 | C | T | 111 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(108): Show |
111 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.754-4489C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720428 | |||||||
chr2:202720604 | CT | C | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.754-4301delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720604 | ||||||
chr2:202720722 | A | G | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.754-4195A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720722 | |||||||
chr2:202720863 | T | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-4054T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720863 | |||||||
chr2:202720890 | C | T | 1 | a0001c0001t0007g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.754-4027C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720890 | |||||||
chr2:202720985 | T | G | 4 | a0001c0001t0020g0021 a0001c0001t0020g0024 a0001c0001t0020g0030 others(1): Show |
4 | HG00741.hp2 HG01106.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-3932T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720985 | |||||||
chr2:202721036 | A | T | 80 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(77): Show |
80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-3881A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721036 | |||||||
chr2:202721127 | A | T | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(98): Show |
101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-3790A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721127 | |||||||
chr2:202721140 | C | CT | 12 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(9): Show |
12 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.754-3768dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202721140 | ||||||
chr2:202721313 | A | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-3604A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721313 | |||||||
chr2:202721321 | A | T | 33 | a0001c0001t0032g0007 a0001c0001t0044g0267 a0001c0001t0107g0266 others(30): Show |
33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.754-3596A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721321 | |||||||
chr2:202721616 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.754-3301A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721616 | |||||||
chr2:202721779 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0009g0256 a0001c0001t0010g0254 |
3 | HG02965.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.754-3138G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721779 | |||||||
chr2:202721810 | T | A | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-3107T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721810 | |||||||
chr2:202721881 | G | C | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-3036G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721881 | |||||||
chr2:202722007 | A | AT | 49 | a0001c0001t0001g0106 a0001c0001t0001g0155 a0001c0001t0001g0215 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.754-2890dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202722007 | ||||||
chr2:202722007 | A | ATT | 6 | a0001c0001t0010g0104 a0001c0001t0019g0036 a0001c0001t0036g0286 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-2891_754-2890d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202722007 | ||||||
chr2:202722071 | C | T | 1 | a0001c0001t0009g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.754-2846C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722071 | |||||||
chr2:202722113 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-2804C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722113 | |||||||
chr2:202722154 | G | C | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.754-2763G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722154 | |||||||
chr2:202722200 | C | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-2717C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722200 | |||||||
chr2:202722776 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.754-2141C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722776 | |||||||
chr2:202723428 | A | G | 1 | a0001c0001t0014g0108 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.754-1489A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723428 | |||||||
chr2:202723441 | C | T | 2 | a0002c0002t0016g0299 a0002c0002t0070g0295 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.754-1476C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723441 | |||||||
chr2:202723474 | A | G | 7 | a0001c0001t0008g0221 a0001c0001t0008g0224 a0001c0001t0008g0226 others(4): Show |
7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-1443A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723474 | |||||||
chr2:202723776 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.754-1141G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723776 | |||||||
chr2:202724051 | C | CT | 252 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.754-842dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | ||||||
chr2:202724051 | C | CTT | 32 | a0001c0001t0001g0253 a0001c0001t0002g0054 a0001c0001t0002g0081 others(29): Show |
32 | HG00621.hp1 HG00738.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.754-843_754-842dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | ||||||
chr2:202724051 | C | CTTT | 11 | a0001c0001t0003g0133 a0001c0001t0034g0185 a0001c0001t0050g0053 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-844_754-842dup others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | ||||||
chr2:202724089 | CCT | C | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.754-825_754-824del others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724089 | ||||||
chr2:202724168 | C | T | 1 | a0001c0001t0040g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.754-749C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724168 | |||||||
chr2:202724264 | C | T | 1 | a0003c0003t0012g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.754-653C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724264 | |||||||
chr2:202724334 | C | T | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-583C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724334 | |||||||
chr2:202724338 | C | T | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.754-579C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724338 | |||||||
chr2:202724584 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-333A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724584 | |||||||
chr2:202724634 | A | C | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-283A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724634 | |||||||
chr2:202724667 | T | TGTAGTAT others(18): Show |
1 | a0001c0001t0013g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.754-249_754-225dup others(25): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724667 | ||||||
chr2:202725229 | A | C | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+220A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202725229 | |||||||
chr2:202725299 | C | CT | 227 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(224): Show |
227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.846+306dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | ||||||
chr2:202725299 | C | CTT | 6 | a0001c0001t0014g0219 a0001c0001t0029g0268 a0001c0001t0029g0269 others(3): Show |
6 | HG03139.hp2 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+305_846+306dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | ||||||
chr2:202725299 | CTTTT | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+303_846+306del others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | ||||||
chr2:202725597 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.846+588G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202725597 | |||||||
chr2:202726066 | A | G | 1 | a0001c0001t0011g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.847-184A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202726066 | |||||||
chr2:202726173 | G | C | 1 | a0001c0001t0005g0122 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.847-77G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202726173 | |||||||
chr2:202726505 | A | T | 1 | a0001c0001t0111g0244 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.960+142A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726505 | |||||||
chr2:202726538 | T | C | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960+175T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726538 | |||||||
chr2:202726802 | A | C | 1 | a0001c0001t0049g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.960+439A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726802 | |||||||
chr2:202726817 | G | A | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.960+454G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726817 | |||||||
chr2:202726893 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.960+530C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726893 | |||||||
chr2:202726946 | T | TA | 6 | a0001c0001t0001g0037 a0001c0001t0001g0105 a0001c0001t0022g0110 others(3): Show |
6 | HG01167.hp2 HG02155.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+594dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202726946 | ||||||
chr2:202726957 | A | T | 1 | a0001c0001t0087g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.960+594A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726957 | |||||||
chr2:202727062 | C | CT | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(25): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.960+707dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202727062 | ||||||
chr2:202727094 | C | T | 1 | a0001c0001t0042g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.960+731C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727094 | |||||||
chr2:202727244 | A | G | 36 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(33): Show |
36 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.960+881A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727244 | |||||||
chr2:202727265 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+902G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727265 | |||||||
chr2:202727423 | C | T | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.960+1060C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727423 | |||||||
chr2:202727457 | A | G | 177 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(174): Show |
177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.960+1094A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727457 | |||||||
chr2:202727487 | A | G | 1 | a0001c0001t0049g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.960+1124A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727487 | |||||||
chr2:202727806 | C | A | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.960+1443C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727806 | |||||||
chr2:202727966 | A | G | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+1603A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727966 | |||||||
chr2:202727997 | G | A | 3 | a0001c0001t0032g0007 a0002c0002t0006g0305 a0002c0002t0006g0306 |
3 | HG02572.hp1 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.960+1634G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727997 | |||||||
chr2:202728049 | GA | G | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.960+1687delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728049 | |||||||
chr2:202728051 | T | C | 39 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.960+1688T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728051 | |||||||
chr2:202728135 | A | G | 1 | a0002c0002t0006g0302 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.960+1772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728135 | |||||||
chr2:202729052 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+2689C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729052 | |||||||
chr2:202729266 | G | A | 1 | a0001c0001t0011g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.960+2903G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729266 | |||||||
chr2:202729333 | CA | C | 100 | a0001c0001t0001g0017 a0001c0001t0001g0123 a0001c0001t0002g0054 others(97): Show |
100 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.960+2983delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202729333 | ||||||
chr2:202729510 | C | T | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.960+3147C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729510 | |||||||
chr2:202729669 | A | G | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+3306A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729669 | |||||||
chr2:202729693 | C | T | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+3330C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729693 | |||||||
chr2:202729724 | T | C | 144 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(141): Show |
144 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.960+3361T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729724 | |||||||
chr2:202729836 | A | G | 27 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(24): Show |
27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.960+3473A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729836 | |||||||
chr2:202730002 | T | G | 1 | a0001c0001t0023g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.960+3639T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730002 | |||||||
chr2:202730435 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0081g0087 |
2 | HG01071.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.960+4072C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730435 | |||||||
chr2:202730647 | G | A | 68 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.960+4284G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730647 | |||||||
chr2:202730675 | A | G | 2 | a0001c0001t0009g0119 a0001c0001t0031g0157 |
2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.960+4312A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730675 | |||||||
chr2:202730704 | G | A | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+4341G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730704 | |||||||
chr2:202730722 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.960+4359A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730722 | |||||||
chr2:202730736 | C | T | 50 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0186 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.960+4373C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730736 | |||||||
chr2:202731087 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.960+4724C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731087 | |||||||
chr2:202731136 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.960+4773G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731136 | |||||||
chr2:202731151 | C | T | 2 | a0001c0004t0038g0012 a0001c0004t0038g0013 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.960+4788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731151 | |||||||
chr2:202731246 | C | A | 1 | a0001c0001t0046g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.960+4883C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731246 | |||||||
chr2:202731332 | A | AAAAAATA others(3): Show |
1 | a0001c0001t0004g0022 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(3): Show |
4 | a0001c0001t0019g0034 a0001c0001t0020g0030 a0001c0001t0072g0025 others(1): Show |
4 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+4970_960+4971i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(5): Show |
4 | a0001c0001t0004g0026 a0001c0001t0004g0029 a0001c0001t0019g0035 others(1): Show |
4 | HG00639.hp1 HG01167.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+4970_960+4971i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(7): Show |
1 | a0001c0001t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(9): Show |
1 | a0001c0001t0020g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(11): Show |
2 | a0001c0001t0004g0031 a0001c0001t0019g0033 |
2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(13): Show |
2 | a0001c0001t0004g0045 a0001c0001t0121g0047 |
2 | HG00609.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(15): Show |
2 | a0001c0001t0004g0027 a0001c0001t0004g0228 |
2 | HG01496.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(17): Show |
2 | a0001c0001t0004g0100 a0001c0001t0117g0046 |
2 | HG01192.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(19): Show |
1 | a0001c0001t0004g0028 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(21): Show |
1 | a0001c0001t0116g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(30): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(25): Show |
1 | a0001c0001t0122g0009 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(34): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AAAATATA others(27): Show |
1 | a0001c0001t0115g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(36): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AACATATA others(19): Show |
1 | a0001c0001t0001g0139 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATAT | 8 | a0001c0001t0001g0196 a0001c0001t0003g0191 a0001c0001t0008g0004 others(5): Show |
8 | HG02622.hp2 NA18950.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+5002_960+5005d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATAT | 14 | a0001c0001t0002g0090 a0001c0001t0005g0003 a0001c0001t0005g0238 others(11): Show |
14 | HG00140.hp1 HG00733.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.960+5000_960+5005d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(1): Show |
17 | a0001c0001t0001g0017 a0001c0001t0002g0093 a0001c0001t0009g0084 others(14): Show |
17 | HG02083.hp1 HG02132.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+4998_960+5005d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(3): Show |
20 | a0001c0001t0001g0106 a0001c0001t0002g0058 a0001c0001t0002g0073 others(17): Show |
20 | HG00099.hp2 HG00621.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.960+4996_960+5005d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(5): Show |
23 | a0001c0001t0001g0147 a0001c0001t0001g0172 a0001c0001t0002g0071 others(20): Show |
23 | HG00099.hp1 HG00673.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.960+4994_960+5005d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(7): Show |
16 | a0001c0001t0002g0065 a0001c0001t0002g0098 a0001c0001t0003g0113 others(13): Show |
16 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.960+4992_960+5005d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(9): Show |
21 | a0001c0001t0001g0253 a0001c0001t0002g0054 a0001c0001t0002g0074 others(18): Show |
21 | HG00323.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.960+4990_960+5005d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(11): Show |
11 | a0001c0001t0001g0146 a0001c0001t0001g0164 a0001c0001t0002g0077 others(8): Show |
11 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+4988_960+5005d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(13): Show |
4 | a0001c0001t0002g0068 a0001c0001t0092g0211 a0003c0003t0012g0062 others(1): Show |
4 | HG00544.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+4986_960+5005d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(15): Show |
2 | a0001c0001t0005g0203 a0001c0001t0017g0197 |
2 | HG04228.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.960+4984_960+5005d others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | A | AATATATA others(17): Show |
1 | a0001c0001t0011g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.960+4982_960+5005d others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AAT | A | 6 | a0001c0001t0050g0053 a0001c0001t0050g0270 a0001c0001t0055g0282 others(3): Show |
6 | HG01891.hp1 HG02080.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+5004_960+5005d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATAT | A | 8 | a0001c0001t0008g0049 a0001c0001t0017g0050 a0001c0001t0029g0269 others(5): Show |
8 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+5002_960+5005d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATAT | A | 17 | a0001c0001t0032g0007 a0001c0007t0068g0285 a0002c0002t0006g0302 others(14): Show |
17 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.960+5000_960+5005d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATATA others(3): Show |
A | 3 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 |
3 | HG02109.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+4996_960+5005d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATATA others(5): Show |
A | 1 | a0001c0001t0077g0210 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.960+4994_960+5005d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATATA others(7): Show |
A | 1 | a0001c0001t0100g0204 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960+4992_960+5005d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATATA others(11): Show |
A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+4988_960+5005d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731332 | AATATATA others(13): Show |
A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+4986_960+5005d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | ||||||
chr2:202731334 | T | A | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+4971T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731334 | |||||||
chr2:202731345 | A | G | 1 | a0001c0001t0049g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.960+4982A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731345 | |||||||
chr2:202731362 | T | TATATATA others(11): Show |
1 | a0001c0001t0079g0240 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | ||||||
chr2:202731362 | T | TATATATA others(15): Show |
1 | a0001c0001t0040g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | ||||||
chr2:202731362 | T | TATATATA others(17): Show |
1 | a0001c0001t0040g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.960+5005_960+5006i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | ||||||
chr2:202731362 | T | TATATATA others(19): Show |
1 | a0001c0001t0024g0222 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | ||||||
chr2:202731368 | T | G | 63 | a0001c0001t0001g0139 a0001c0001t0003g0153 a0001c0001t0004g0019 others(60): Show |
63 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.960+5005T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATAG | 6 | a0001c0001t0001g0114 a0001c0001t0001g0220 a0001c0001t0008g0226 others(3): Show |
6 | HG01952.hp2 HG02155.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATAG | 5 | a0001c0001t0001g0120 a0001c0001t0009g0010 a0001c0001t0025g0213 others(2): Show |
5 | HG00558.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(1): Show |
28 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0105 others(25): Show |
28 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(3): Show |
24 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0155 others(21): Show |
24 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(5): Show |
11 | a0001c0001t0001g0061 a0001c0001t0001g0141 a0001c0001t0001g0167 others(8): Show |
11 | HG02165.hp1 HG02723.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(7): Show |
10 | a0001c0001t0001g0117 a0001c0001t0001g0156 a0001c0001t0013g0041 others(7): Show |
10 | HG00609.hp2 HG02080.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(9): Show |
4 | a0001c0001t0001g0144 a0001c0001t0010g0104 a0001c0001t0045g0171 others(1): Show |
4 | HG02572.hp2 HG02970.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(11): Show |
2 | a0001c0001t0009g0107 a0001c0001t0045g0112 |
2 | HG04199.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.960+5005_960+5006i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(13): Show |
1 | a0001c0001t0034g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731368 | T | TATATATA others(17): Show |
1 | a0001c0001t0082g0231 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | |||||||
chr2:202731523 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+5160C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731523 | |||||||
chr2:202731602 | T | C | 1 | a0002c0002t0006g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.960+5239T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731602 | |||||||
chr2:202731722 | A | G | 1 | a0001c0001t0023g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.960+5359A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731722 | |||||||
chr2:202731761 | G | A | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+5398G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731761 | |||||||
chr2:202732046 | C | CT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0253 others(13): Show |
16 | HG00140.hp2 HG00597.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+5699dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732046 | ||||||
chr2:202732105 | G | A | 2 | a0002c0002t0059g0316 a0002c0002t0060g0317 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.960+5742G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732105 | |||||||
chr2:202732180 | C | T | 1 | a0001c0001t0055g0282 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.960+5817C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732180 | |||||||
chr2:202732202 | A | G | 1 | a0001c0001t0097g0039 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.960+5839A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732202 | |||||||
chr2:202732275 | T | C | 1 | a0001c0001t0003g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.960+5912T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732275 | |||||||
chr2:202732376 | A | G | 1 | a0003c0003t0012g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+6013A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732376 | |||||||
chr2:202732546 | C | T | 28 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(25): Show |
28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.960+6183C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732546 | |||||||
chr2:202732686 | C | T | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+6323C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732686 | |||||||
chr2:202732691 | C | T | 100 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(97): Show |
100 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.960+6328C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732691 | |||||||
chr2:202732723 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.960+6360C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732723 | |||||||
chr2:202732725 | G | A | 1 | a0001c0001t0042g0257 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.960+6362G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732725 | |||||||
chr2:202732752 | C | T | 5 | a0002c0002t0021g0289 a0002c0002t0021g0290 a0002c0002t0021g0291 others(2): Show |
5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+6389C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732752 | |||||||
chr2:202732763 | C | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+6400C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732763 | |||||||
chr2:202732777 | C | G | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+6414C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732777 | |||||||
chr2:202732815 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.960+6452C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732815 | |||||||
chr2:202732826 | G | GTAAA | 7 | a0001c0001t0001g0136 a0001c0001t0003g0158 a0001c0001t0009g0165 others(4): Show |
7 | HG01081.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+6492_960+6495d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732826 | ||||||
chr2:202732826 | GTAAA | G | 121 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0002g0054 others(118): Show |
121 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.960+6492_960+6495d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732826 | ||||||
chr2:202732834 | A | G | 73 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0002g0054 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.960+6471A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732834 | |||||||
chr2:202732873 | TA | T | 121 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0002g0054 others(118): Show |
121 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.960+6524delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732873 | ||||||
chr2:202732939 | T | C | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.960+6576T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732939 | |||||||
chr2:202733177 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.960+6814G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733177 | |||||||
chr2:202733204 | G | C | 1 | a0001c0001t0008g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960+6841G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733204 | |||||||
chr2:202733278 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+6915T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733278 | |||||||
chr2:202733396 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.960+7033A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733396 | |||||||
chr2:202733556 | A | G | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+7193A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733556 | |||||||
chr2:202733602 | G | A | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+7239G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733602 | |||||||
chr2:202733606 | A | G | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7243A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733606 | |||||||
chr2:202733651 | C | T | 6 | a0002c0002t0016g0296 a0002c0002t0016g0299 a0002c0002t0066g0300 others(3): Show |
6 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+7288C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733651 | |||||||
chr2:202733739 | C | T | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.960+7376C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733739 | |||||||
chr2:202733744 | T | G | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.960+7381T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733744 | |||||||
chr2:202733835 | C | T | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.960+7472C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733835 | |||||||
chr2:202733936 | T | A | 76 | a0001c0001t0001g0017 a0001c0001t0001g0164 a0001c0001t0002g0054 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.960+7573T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733936 | |||||||
chr2:202734054 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7691G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734054 | |||||||
chr2:202734077 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+7714G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734077 | |||||||
chr2:202734113 | G | A | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.960+7750G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734113 | |||||||
chr2:202734124 | A | C | 1 | a0003c0003t0032g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.960+7761A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734124 | |||||||
chr2:202734221 | A | G | 1 | a0001c0001t0099g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.960+7858A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734221 | |||||||
chr2:202734274 | C | G | 4 | a0001c0001t0015g0271 a0001c0001t0052g0274 a0001c0001t0053g0273 others(1): Show |
4 | NA18939.hp2 NA18974.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7911C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734274 | |||||||
chr2:202734422 | A | G | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+8059A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734422 | |||||||
chr2:202734643 | G | T | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+8280G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734643 | |||||||
chr2:202734672 | G | A | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960+8309G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734672 | |||||||
chr2:202734902 | G | A | 4 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0001c0001t0064g0284 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+8539G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734902 | |||||||
chr2:202735145 | T | C | 31 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(28): Show |
31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+8782T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735145 | |||||||
chr2:202735269 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.960+8906G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735269 | |||||||
chr2:202735366 | A | G | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+9003A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735366 | |||||||
chr2:202735789 | T | G | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+9426T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735789 | |||||||
chr2:202735934 | C | T | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+9571C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735934 | |||||||
chr2:202735999 | C | T | 1 | a0001c0001t0080g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.960+9636C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735999 | |||||||
chr2:202736076 | A | G | 2 | a0001c0001t0044g0267 a0001c0001t0107g0266 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.960+9713A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736076 | |||||||
chr2:202736508 | C | T | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960+10145C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736508 | |||||||
chr2:202736526 | C | T | 1 | a0003c0003t0012g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+10163C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736526 | |||||||
chr2:202736586 | C | T | 37 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0186 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.960+10223C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736586 | |||||||
chr2:202736711 | G | C | 2 | a0001c0001t0029g0268 a0001c0001t0029g0269 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+10348G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736711 | |||||||
chr2:202736873 | C | T | 4 | a0001c0001t0005g0003 a0001c0001t0008g0004 a0001c0001t0028g0002 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+10510C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736873 | |||||||
chr2:202736911 | TA | T | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+10559delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202736911 | ||||||
chr2:202736931 | A | G | 1 | a0001c0001t0018g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.960+10568A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736931 | |||||||
chr2:202737158 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.960+10795C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737158 | |||||||
chr2:202737170 | TA | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0105 a0001c0001t0002g0085 others(4): Show |
7 | HG02738.hp2 HG03017.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+10819delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202737170 | ||||||
chr2:202737319 | G | T | 1 | a0001c0001t0084g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+10956G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737319 | |||||||
chr2:202737338 | A | G | 3 | a0001c0001t0025g0259 a0001c0001t0025g0261 a0001c0001t0086g0265 |
3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.960+10975A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737338 | |||||||
chr2:202737444 | C | G | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.960+11081C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737444 | |||||||
chr2:202737484 | C | A | 147 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.960+11121C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737484 | |||||||
chr2:202737495 | A | C | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+11132A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737495 | |||||||
chr2:202737607 | CT | C | 6 | a0002c0002t0006g0313 a0002c0002t0021g0289 a0002c0002t0021g0290 others(3): Show |
6 | HG01169.hp1 HG01884.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+11256delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202737607 | ||||||
chr2:202737633 | G | T | 2 | a0001c0001t0095g0199 a0001c0001t0100g0204 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.960+11270G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737633 | |||||||
chr2:202737767 | A | C | 1 | a0001c0001t0015g0276 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.960+11404A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737767 | |||||||
chr2:202737781 | T | C | 1 | a0001c0001t0005g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.960+11418T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737781 | |||||||
chr2:202737826 | G | T | 147 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0058 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.960+11463G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737826 | |||||||
chr2:202737894 | G | A | 1 | a0002c0002t0061g0310 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.960+11531G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737894 | |||||||
chr2:202737927 | A | G | 1 | a0001c0001t0009g0107 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.960+11564A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737927 | |||||||
chr2:202737956 | G | A | 1 | a0001c0001t0084g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+11593G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737956 | |||||||
chr2:202738458 | G | A | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+12095G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738458 | |||||||
chr2:202738512 | T | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+12149T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738512 | |||||||
chr2:202738732 | A | G | 14 | a0001c0001t0003g0042 a0001c0001t0004g0019 a0001c0001t0004g0020 others(11): Show |
14 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.960+12369A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738732 | |||||||
chr2:202738872 | A | G | 1 | a0001c0001t0084g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+12509A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738872 | |||||||
chr2:202738908 | G | A | 7 | a0002c0002t0016g0296 a0002c0002t0016g0297 a0002c0002t0016g0299 others(4): Show |
7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+12545G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738908 | |||||||
chr2:202738991 | C | G | 3 | a0001c0001t0017g0040 a0001c0001t0051g0111 a0001c0001t0051g0179 |
3 | HG00140.hp1 HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.960+12628C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738991 | |||||||
chr2:202739235 | G | C | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+12872G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739235 | |||||||
chr2:202739257 | A | G | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960+12894A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739257 | |||||||
chr2:202739307 | G | A | 4 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+12944G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739307 | |||||||
chr2:202739317 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0023g0135 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.960+12954A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739317 | |||||||
chr2:202739356 | T | A | 1 | a0001c0001t0004g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.960+12993T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739356 | |||||||
chr2:202739392 | CGTCTGTC others(5): Show |
C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0217 a0001c0001t0009g0107 others(2): Show |
5 | HG02080.hp2 NA18962.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+13039_960+1305 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202739392 | ||||||
chr2:202739554 | C | T | 1 | a0001c0001t0087g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.960+13191C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739554 | |||||||
chr2:202739601 | G | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0098 a0001c0001t0007g0072 |
3 | HG00408.hp2 HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.960+13238G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739601 | |||||||
chr2:202739645 | C | T | 30 | a0001c0001t0032g0007 a0002c0002t0006g0302 a0002c0002t0006g0305 others(27): Show |
30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.960+13282C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739645 | |||||||
chr2:202740166 | T | C | 4 | a0001c0001t0036g0286 a0001c0001t0036g0287 a0001c0001t0063g0288 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+13803T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740166 | |||||||
chr2:202740173 | C | CA | 6 | a0001c0001t0002g0058 a0001c0001t0002g0090 a0001c0001t0008g0004 others(3): Show |
6 | HG02055.hp2 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAA | 23 | a0001c0001t0001g0017 a0001c0001t0002g0054 a0001c0001t0002g0065 others(20): Show |
23 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAA | 30 | a0001c0001t0002g0068 a0001c0001t0002g0073 a0001c0001t0002g0074 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAA | 28 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0176 others(25): Show |
28 | HG00544.hp2 HG00639.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAA | 50 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0061 others(47): Show |
50 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA | 43 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0123 others(40): Show |
43 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA others(1): Show |
29 | a0001c0001t0001g0136 a0001c0001t0001g0160 a0001c0001t0001g0255 others(26): Show |
29 | HG00673.hp1 HG00733.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0043 a0001c0001t0001g0172 a0001c0001t0001g0217 others(9): Show |
12 | HG00741.hp1 HG01081.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA others(3): Show |
8 | a0001c0001t0010g0104 a0001c0001t0028g0161 a0001c0001t0030g0127 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0038 a0001c0001t0005g0118 a0001c0001t0030g0128 |
3 | HG02109.hp2 HG06807.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.960+13810_960+1381 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0003g0089 a0001c0001t0046g0168 |
2 | HG04204.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.960+13810_960+1381 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | CCAAAAAA others(4): Show |
C | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.960+13811_960+1382 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740173 | CCAAAAAA others(5): Show |
C | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+13811_960+1382 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | |||||||
chr2:202740174 | C | A | 237 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(234): Show |
237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.960+13811C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740174 | |||||||
chr2:202740174 | C | CA | 17 | a0001c0001t0005g0051 a0001c0001t0005g0122 a0001c0001t0005g0206 others(14): Show |
17 | HG00544.hp1 HG00597.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+13839dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740174 | ||||||
chr2:202740175 | A | C | 2 | a0001c0001t0001g0253 a0001c0001t0091g0188 |
2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.960+13812A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740175 | |||||||
chr2:202740176 | A | C | 3 | a0001c0001t0001g0253 a0001c0001t0026g0251 a0001c0001t0026g0252 |
3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.960+13813A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740176 | |||||||
chr2:202740261 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0101g0174 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.960+13898G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740261 | |||||||
chr2:202740279 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.960+13916G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740279 | |||||||
chr2:202740292 | G | A | 1 | a0001c0001t0099g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.960+13929G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740292 | |||||||
chr2:202740359 | C | CA | 92 | a0001c0001t0001g0017 a0001c0001t0001g0166 a0001c0001t0002g0054 others(89): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.960+14017dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | ||||||
chr2:202740359 | C | CAA | 7 | a0001c0001t0002g0090 a0001c0001t0015g0271 a0001c0001t0119g0023 others(4): Show |
7 | HG00642.hp1 HG03130.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+14016_960+1401 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | ||||||
chr2:202740359 | CA | C | 14 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0191 others(11): Show |
14 | HG02258.hp2 HG02523.hp1 HG03471.hp2 others(11): Show |
intron_variant | MODIFIER | c.960+14017delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | ||||||
chr2:202740359 | CAA | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+14016_960+1401 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | ||||||
chr2:202740388 | A | G | 1 | a0001c0001t0088g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.960+14025A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740388 | |||||||
chr2:202740436 | T | G | 1 | a0001c0001t0033g0277 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.960+14073T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740436 | |||||||
chr2:202740863 | C | CA | 5 | a0001c0001t0009g0010 a0001c0001t0009g0165 a0001c0001t0009g0169 others(2): Show |
5 | HG00558.hp1 HG01243.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+14509dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740863 | ||||||
chr2:202740994 | T | TG | 8 | a0001c0001t0029g0079 a0001c0001t0029g0268 a0001c0001t0029g0269 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-14540dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740994 | ||||||
chr2:202741191 | G | A | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.961-14347G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741191 | |||||||
chr2:202741231 | T | G | 6 | a0001c0001t0029g0269 a0002c0002t0021g0289 a0002c0002t0021g0290 others(3): Show |
6 | HG01884.hp2 HG03130.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-14307T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741231 | |||||||
chr2:202741344 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.961-14194G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741344 | |||||||
chr2:202741416 | C | CA | 27 | a0001c0001t0001g0117 a0001c0001t0001g0156 a0001c0001t0005g0003 others(24): Show |
27 | HG00099.hp2 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.961-14092dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | C | CAAA | 10 | a0001c0001t0005g0051 a0001c0001t0005g0234 a0001c0001t0005g0238 others(7): Show |
10 | HG00597.hp2 HG00738.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-14094_961-1409 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CA | C | 62 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(59): Show |
62 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.961-14092delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAA | C | 17 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0141 others(14): Show |
17 | HG00673.hp1 HG01081.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.961-14093_961-1409 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAAAA | C | 13 | a0001c0001t0001g0253 a0001c0001t0004g0020 a0001c0001t0004g0026 others(10): Show |
13 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.961-14095_961-1409 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAAAAA | C | 50 | a0001c0001t0001g0164 a0001c0001t0002g0077 a0001c0001t0002g0085 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.961-14096_961-1409 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAAAAAA | C | 62 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.961-14097_961-1409 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAAAAAAA others(5): Show |
C | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-14103_961-1409 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741416 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0119g0023 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.961-14107_961-1409 others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | ||||||
chr2:202741492 | G | A | 129 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.961-14046G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741492 | |||||||
chr2:202741542 | A | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-13996A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741542 | |||||||
chr2:202741542 | AT | A | 8 | a0001c0001t0005g0203 a0001c0001t0008g0221 a0001c0001t0008g0224 others(5): Show |
8 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-13984delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741542 | ||||||
chr2:202741542 | ATTTTTT | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13989_961-1398 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741542 | ||||||
chr2:202741552 | T | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13986T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741552 | |||||||
chr2:202741553 | T | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13985T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741553 | |||||||
chr2:202741555 | G | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13983G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741555 | |||||||
chr2:202741557 | G | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13981G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741557 | |||||||
chr2:202741600 | G | A | 1 | a0001c0001t0028g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.961-13938G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741600 | |||||||
chr2:202741605 | C | T | 129 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.961-13933C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741605 | |||||||
chr2:202741682 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.961-13856G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741682 | |||||||
chr2:202741693 | C | T | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-13845C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741693 | |||||||
chr2:202741871 | CA | C | 3 | a0001c0001t0022g0110 a0001c0001t0022g0194 a0001c0001t0078g0096 |
3 | HG02155.hp1 NA18747.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.961-13665delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741871 | ||||||
chr2:202741886 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.961-13652A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741886 | |||||||
chr2:202742031 | T | C | 132 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.961-13507T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742031 | |||||||
chr2:202742132 | A | C | 24 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0141 others(21): Show |
24 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.961-13406A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742132 | |||||||
chr2:202742278 | C | T | 1 | a0003c0003t0012g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961-13260C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742278 | |||||||
chr2:202742530 | C | T | 1 | a0001c0001t0008g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.961-13008C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742530 | |||||||
chr2:202742566 | C | T | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-12972C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742566 | |||||||
chr2:202742599 | T | A | 128 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.961-12939T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742599 | |||||||
chr2:202742600 | C | A | 128 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.961-12938C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742600 | |||||||
chr2:202742664 | A | G | 1 | a0001c0001t0045g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.961-12874A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742664 | |||||||
chr2:202742732 | CAG | C | 8 | a0001c0001t0029g0079 a0001c0001t0029g0268 a0001c0001t0029g0269 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-12804_961-1280 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202742732 | ||||||
chr2:202742752 | T | C | 1 | a0001c0001t0005g0238 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.961-12786T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742752 | |||||||
chr2:202742850 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.961-12688A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742850 | |||||||
chr2:202743050 | C | T | 1 | a0001c0001t0040g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.961-12488C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743050 | |||||||
chr2:202743307 | A | G | 1 | a0001c0001t0011g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.961-12231A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743307 | |||||||
chr2:202743385 | A | G | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-12153A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743385 | |||||||
chr2:202743442 | T | C | 1 | a0001c0001t0027g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-12096T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743442 | |||||||
chr2:202743450 | G | A | 1 | a0001c0001t0044g0267 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.961-12088G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743450 | |||||||
chr2:202743467 | A | G | 115 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.961-12071A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743467 | |||||||
chr2:202743595 | T | C | 2 | a0001c0001t0063g0288 a0001c0007t0068g0285 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.961-11943T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743595 | |||||||
chr2:202743621 | G | T | 1 | a0001c0001t0003g0149 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.961-11917G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743621 | |||||||
chr2:202743626 | C | CAAAT | 55 | a0001c0001t0001g0253 a0001c0001t0004g0019 a0001c0001t0004g0020 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.961-11909_961-1190 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202743626 | ||||||
chr2:202743630 | C | T | 76 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0002g0054 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.961-11908C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743630 | |||||||
chr2:202743699 | A | C | 4 | a0001c0001t0024g0222 a0001c0001t0040g0195 a0001c0001t0040g0208 others(1): Show |
4 | HG02293.hp1 HG02300.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-11839A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743699 | |||||||
chr2:202743834 | C | T | 1 | a0001c0001t0004g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.961-11704C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743834 | |||||||
chr2:202744019 | T | C | 131 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.961-11519T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744019 | |||||||
chr2:202744047 | A | G | 8 | a0001c0001t0005g0118 a0002c0002t0016g0296 a0002c0002t0016g0297 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-11491A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744047 | |||||||
chr2:202744053 | G | T | 1 | a0001c0001t0093g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.961-11485G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744053 | |||||||
chr2:202744155 | T | TCTTA | 78 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(75): Show |
78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.961-11382_961-1137 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744155 | ||||||
chr2:202744250 | A | G | 2 | a0001c0001t0036g0286 a0001c0001t0036g0287 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.961-11288A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744250 | |||||||
chr2:202744403 | C | T | 2 | a0001c0001t0026g0251 a0001c0001t0026g0252 |
2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.961-11135C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744403 | |||||||
chr2:202744461 | A | G | 2 | a0001c0001t0015g0275 a0001c0001t0056g0280 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.961-11077A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744461 | |||||||
chr2:202744590 | G | A | 1 | a0001c0001t0045g0171 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.961-10948G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744590 | |||||||
chr2:202744706 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0123 a0001c0001t0009g0084 others(1): Show |
4 | HG03017.hp2 HG03491.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-10832C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744706 | |||||||
chr2:202744960 | G | C | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-10578G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744960 | |||||||
chr2:202744976 | C | CA | 17 | a0001c0001t0001g0106 a0001c0001t0001g0155 a0001c0001t0001g0166 others(14): Show |
17 | HG00597.hp1 HG00621.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-10539dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | ||||||
chr2:202744976 | CA | C | 18 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0217 others(15): Show |
18 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-10539delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | ||||||
chr2:202744976 | CAA | C | 95 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(92): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.961-10540_961-1053 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | ||||||
chr2:202744976 | CAAA | C | 25 | a0001c0001t0001g0253 a0001c0001t0004g0019 a0001c0001t0004g0022 others(22): Show |
25 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.961-10541_961-1053 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | ||||||
chr2:202745000 | G | T | 1 | a0001c0001t0039g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-10538G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745000 | |||||||
chr2:202745053 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.961-10485A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745053 | |||||||
chr2:202745060 | T | TCA | 131 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.961-10477_961-1047 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202745060 | ||||||
chr2:202745279 | CA | C | 30 | a0001c0001t0001g0196 a0001c0001t0003g0191 a0001c0001t0005g0118 others(27): Show |
30 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.961-10245delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202745279 | ||||||
chr2:202745295 | G | A | 1 | a0002c0002t0060g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-10243G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745295 | |||||||
chr2:202745649 | A | G | 1 | a0002c0002t0006g0314 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.961-9889A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745649 | |||||||
chr2:202745682 | T | C | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-9856T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745682 | |||||||
chr2:202745741 | G | T | 1 | a0001c0001t0005g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.961-9797G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745741 | |||||||
chr2:202745967 | A | T | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-9571A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745967 | |||||||
chr2:202746107 | A | G | 30 | a0001c0001t0001g0253 a0001c0001t0004g0019 a0001c0001t0004g0020 others(27): Show |
30 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.961-9431A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746107 | |||||||
chr2:202746217 | A | C | 76 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0002g0054 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.961-9321A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746217 | |||||||
chr2:202746379 | A | T | 235 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(232): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.961-9159A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746379 | |||||||
chr2:202746498 | TA | T | 131 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.961-9031delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746498 | ||||||
chr2:202746946 | C | T | 1 | a0001c0001t0041g0193 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.961-8592C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746946 | |||||||
chr2:202746948 | GA | G | 128 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.961-8581delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746948 | ||||||
chr2:202746948 | GAAAAAAA others(9): Show |
G | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-8581_961-8566d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746948 | ||||||
chr2:202746957 | ACAAAACA others(9): Show |
A | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-8580_961-8565d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746957 | |||||||
chr2:202746960 | AAAC | A | 74 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0002g0054 others(71): Show |
74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.961-8575_961-8573d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746960 | ||||||
chr2:202746961 | AAC | A | 50 | a0001c0001t0001g0253 a0001c0001t0004g0019 a0001c0001t0004g0020 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.961-8575_961-8574d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746961 | ||||||
chr2:202746962 | A | C | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8576A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746962 | |||||||
chr2:202746963 | C | A | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8575C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746963 | |||||||
chr2:202747001 | C | G | 18 | a0001c0001t0032g0007 a0001c0007t0068g0285 a0001c0008t0074g0116 others(15): Show |
18 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-8537C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747001 | |||||||
chr2:202747078 | G | A | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8460G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747078 | |||||||
chr2:202747160 | A | G | 1 | a0001c0001t0088g0198 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.961-8378A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747160 | |||||||
chr2:202747374 | G | A | 4 | a0001c0001t0019g0033 a0001c0001t0019g0034 a0001c0001t0019g0035 others(1): Show |
4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-8164G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747374 | |||||||
chr2:202747530 | A | G | 1 | a0001c0001t0029g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.961-8008A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747530 | |||||||
chr2:202747681 | A | C | 234 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(231): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.961-7857A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747681 | |||||||
chr2:202747706 | G | A | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-7832G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747706 | |||||||
chr2:202747718 | C | G | 1 | a0001c0001t0018g0192 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.961-7820C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747718 | |||||||
chr2:202747766 | A | G | 2 | a0001c0007t0068g0285 a0001c0008t0074g0116 |
2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.961-7772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747766 | |||||||
chr2:202747916 | G | C | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.961-7622G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747916 | |||||||
chr2:202748016 | C | T | 1 | a0001c0001t0043g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.961-7522C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748016 | |||||||
chr2:202748543 | A | T | 7 | a0001c0001t0026g0124 a0001c0001t0028g0161 a0001c0001t0030g0005 others(4): Show |
7 | HG02818.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-6995A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748543 | |||||||
chr2:202748860 | C | A | 1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.961-6678C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748860 | |||||||
chr2:202749054 | AAAAT | A | 5 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-6479_961-6476d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202749054 | ||||||
chr2:202749139 | A | G | 1 | a0003c0003t0012g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961-6399A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749139 | |||||||
chr2:202749400 | C | T | 1 | a0001c0001t0049g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.961-6138C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749400 | |||||||
chr2:202749442 | TA | T | 154 | a0001c0001t0001g0114 a0001c0001t0001g0253 a0001c0001t0002g0054 others(151): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.961-6084delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202749442 | ||||||
chr2:202749827 | C | G | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-5711C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749827 | |||||||
chr2:202749921 | G | A | 1 | a0001c0001t0005g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.961-5617G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749921 | |||||||
chr2:202750231 | G | C | 234 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(231): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.961-5307G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750231 | |||||||
chr2:202750577 | A | G | 1 | a0001c0001t0013g0170 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.961-4961A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750577 | |||||||
chr2:202750728 | T | C | 1 | a0001c0001t0029g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.961-4810T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750728 | |||||||
chr2:202751374 | G | T | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.961-4164G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751374 | |||||||
chr2:202751771 | CA | C | 161 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.961-3744delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | ||||||
chr2:202751771 | CAA | C | 94 | a0001c0001t0001g0061 a0001c0001t0001g0114 a0001c0001t0001g0139 others(91): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.961-3745_961-3744d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | ||||||
chr2:202751771 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0001c0001t0064g0284 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-3756_961-3744d others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | ||||||
chr2:202751793 | A | T | 2 | a0001c0001t0010g0254 a0001c0001t0028g0162 |
2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.961-3745A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751793 | |||||||
chr2:202751881 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.961-3657T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751881 | |||||||
chr2:202751911 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-3627A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751911 | |||||||
chr2:202751920 | C | G | 2 | a0001c0001t0028g0002 a0001c0001t0047g0006 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.961-3618C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751920 | |||||||
chr2:202752206 | C | T | 1 | a0001c0001t0004g0031 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.961-3332C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752206 | |||||||
chr2:202752316 | T | C | 2 | a0001c0001t0107g0266 a0002c0002t0067g0315 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.961-3222T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752316 | |||||||
chr2:202752317 | C | G | 10 | a0001c0001t0029g0079 a0001c0001t0029g0268 a0001c0001t0029g0269 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-3221C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752317 | |||||||
chr2:202752416 | C | CT | 86 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0002g0054 others(83): Show |
86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.961-3106dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202752416 | ||||||
chr2:202752416 | CT | C | 14 | a0001c0001t0005g0118 a0001c0001t0008g0224 a0001c0001t0029g0079 others(11): Show |
14 | HG01168.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.961-3106delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202752416 | ||||||
chr2:202752718 | G | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-2820G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752718 | |||||||
chr2:202752736 | G | A | 1 | a0001c0001t0104g0236 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.961-2802G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752736 | |||||||
chr2:202752999 | C | T | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-2539C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752999 | |||||||
chr2:202753240 | A | G | 4 | a0001c0001t0010g0104 a0001c0001t0010g0214 a0001c0001t0064g0284 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-2298A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753240 | |||||||
chr2:202753408 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0023g0086 a0001c0001t0039g0015 |
3 | HG00099.hp1 HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.961-2130A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753408 | |||||||
chr2:202753548 | A | C | 1 | a0001c0008t0074g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-1990A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753548 | |||||||
chr2:202753558 | A | T | 1 | a0001c0001t0072g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.961-1980A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753558 | |||||||
chr2:202753753 | T | TA | 22 | a0001c0001t0001g0164 a0001c0001t0002g0065 a0001c0001t0004g0228 others(19): Show |
22 | HG00558.hp2 HG00609.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.961-1772dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202753753 | ||||||
chr2:202753753 | TA | T | 6 | a0001c0001t0080g0150 a0002c0002t0021g0289 a0002c0002t0021g0290 others(3): Show |
6 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-1772delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202753753 | ||||||
chr2:202753784 | C | G | 1 | a0001c0001t0029g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.961-1754C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753784 | |||||||
chr2:202753784 | C | T | 1 | a0001c0001t0083g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.961-1754C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753784 | |||||||
chr2:202753986 | G | C | 133 | a0001c0001t0001g0114 a0001c0001t0001g0164 a0001c0001t0001g0253 others(130): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.961-1552G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753986 | |||||||
chr2:202754056 | A | G | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-1482A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754056 | |||||||
chr2:202754360 | C | T | 1 | a0001c0001t0039g0239 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-1178C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754360 | |||||||
chr2:202754385 | A | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-1153A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754385 | |||||||
chr2:202754465 | G | T | 1 | a0002c0002t0006g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.961-1073G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754465 | |||||||
chr2:202754503 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.961-1035A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754503 | |||||||
chr2:202754519 | C | A | 1 | a0002c0002t0060g0317 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-1019C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754519 | |||||||
chr2:202754664 | G | A | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-874G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754664 | |||||||
chr2:202754732 | C | A | 11 | a0001c0001t0005g0051 a0001c0001t0005g0234 a0001c0001t0005g0238 others(8): Show |
11 | HG00597.hp2 HG00738.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-806C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754732 | |||||||
chr2:202754868 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.961-670T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754868 | |||||||
chr2:202754888 | C | CA | 15 | a0001c0001t0005g0118 a0001c0001t0005g0206 a0001c0001t0008g0049 others(12): Show |
15 | HG00738.hp2 HG01243.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.961-631dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | ||||||
chr2:202754888 | C | CAA | 24 | a0001c0001t0001g0043 a0001c0001t0001g0146 a0001c0001t0001g0255 others(21): Show |
24 | HG01081.hp1 HG01192.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-632_961-631dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | ||||||
chr2:202754888 | C | CAAA | 191 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0060 others(188): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.961-633_961-631dup others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | ||||||
chr2:202754888 | C | CAAAA | 13 | a0001c0001t0001g0017 a0001c0001t0003g0191 a0001c0001t0009g0084 others(10): Show |
13 | HG02055.hp2 HG02165.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.961-634_961-631dup others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | ||||||
chr2:202754954 | C | T | 34 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0172 others(31): Show |
34 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.961-584C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754954 | |||||||
chr2:202755100 | G | A | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-438G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755100 | |||||||
chr2:202755245 | C | T | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-293C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755245 | |||||||
chr2:202755311 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0063g0288 |
2 | HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.961-227G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755311 | |||||||
chr2:202755510 | C | T | 5 | a0001c0001t0034g0184 a0001c0001t0034g0185 a0001c0001t0035g0183 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-28C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755510 | |||||||
chr2:202755723 | A | C | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1104+42A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202755723 | |||||||
chr2:202755862 | T | G | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1104+181T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202755862 | |||||||
chr2:202756234 | T | C | 2 | a0001c0001t0010g0104 a0003c0003t0010g0103 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1104+553T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756234 | |||||||
chr2:202756391 | A | G | 1 | a0001c0001t0003g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1104+710A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756391 | |||||||
chr2:202756500 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1105-713G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756500 | |||||||
chr2:202757033 | C | T | 126 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(123): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1105-180C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757033 | |||||||
chr2:202757077 | A | C | 76 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1105-136A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757077 | |||||||
chr2:202757179 | T | C | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1105-34T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757179 | |||||||
chr2:202757468 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1330+30T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757468 | |||||||
chr2:202757698 | A | G | 8 | a0001c0001t0083g0102 a0003c0003t0012g0062 a0003c0003t0012g0246 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1330+260A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757698 | |||||||
chr2:202757927 | A | G | 2 | a0001c0001t0029g0079 a0001c0001t0029g0268 |
2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1330+489A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757927 | |||||||
chr2:202758543 | T | C | 3 | a0001c0001t0107g0266 a0001c0007t0068g0285 a0001c0008t0074g0116 |
3 | HG01884.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331-690T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758543 | |||||||
chr2:202758563 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1331-670A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758563 | |||||||
chr2:202758954 | A | C | 2 | a0002c0002t0016g0299 a0002c0002t0070g0295 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1331-279A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758954 | |||||||
chr2:202759364 | C | T | 1 | a0001c0001t0091g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1451+11C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759364 | |||||||
chr2:202759374 | C | T | 1 | a0002c0002t0058g0318 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1451+21C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759374 | |||||||
chr2:202759543 | C | A | 2 | a0001c0001t0050g0053 a0001c0001t0050g0270 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1451+190C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759543 | |||||||
chr2:202759557 | AT | A | 95 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(92): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1451+222delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202759557 | ||||||
chr2:202759557 | ATT | A | 31 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1451+221_1451+222d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202759557 | ||||||
chr2:202759786 | T | A | 1 | a0001c0001t0085g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1451+433T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759786 | |||||||
chr2:202759860 | C | T | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1451+507C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759860 | |||||||
chr2:202759880 | T | G | 1 | a0001c0001t0039g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1451+527T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759880 | |||||||
chr2:202760182 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1451+829C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760182 | |||||||
chr2:202760279 | G | C | 131 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1451+926G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760279 | |||||||
chr2:202760401 | G | A | 1 | a0001c0001t0084g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1451+1048G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760401 | |||||||
chr2:202760528 | A | G | 1 | a0001c0001t0027g0233 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1451+1175A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760528 | |||||||
chr2:202760567 | T | C | 1 | a0001c0001t0107g0266 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1451+1214T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760567 | |||||||
chr2:202760760 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0105 others(3): Show |
6 | HG00323.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451+1407G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760760 | |||||||
chr2:202760779 | T | G | 1 | a0001c0001t0091g0188 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1451+1426T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760779 | |||||||
chr2:202761143 | T | C | 132 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1451+1790T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761143 | |||||||
chr2:202761572 | G | C | 1 | a0001c0001t0063g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1451+2219G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761572 | |||||||
chr2:202761596 | G | T | 1 | a0001c0001t0114g0237 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1451+2243G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761596 | |||||||
chr2:202761878 | CT | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0144 a0001c0001t0001g0156 others(4): Show |
7 | HG03130.hp1 HG03195.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1451+2537delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202761878 | ||||||
chr2:202761890 | T | A | 6 | a0001c0001t0001g0196 a0001c0001t0003g0042 a0001c0001t0003g0186 others(3): Show |
6 | HG02523.hp1 NA18949.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451+2537T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761890 | |||||||
chr2:202761956 | C | T | 1 | a0001c0001t0034g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1451+2603C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761956 | |||||||
chr2:202762105 | C | T | 1 | a0001c0001t0048g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1451+2752C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762105 | |||||||
chr2:202762114 | C | T | 128 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1451+2761C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762114 | |||||||
chr2:202762442 | C | G | 127 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1452-3004C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762442 | |||||||
chr2:202762522 | T | C | 1 | a0001c0001t0013g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1452-2924T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762522 | |||||||
chr2:202762588 | G | A | 127 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1452-2858G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762588 | |||||||
chr2:202762688 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1452-2758C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762688 | |||||||
chr2:202762689 | C | T | 107 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1452-2757C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762689 | |||||||
chr2:202762716 | A | G | 1 | a0001c0001t0047g0225 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1452-2730A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762716 | |||||||
chr2:202763070 | C | CT | 6 | a0001c0001t0004g0029 a0001c0001t0019g0036 a0001c0001t0044g0267 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1452-2357dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202763070 | ||||||
chr2:202763070 | CT | C | 179 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1452-2357delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202763070 | ||||||
chr2:202763073 | T | C | 1 | a0001c0001t0005g0234 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1452-2373T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763073 | |||||||
chr2:202763164 | C | T | 30 | a0001c0001t0004g0019 a0001c0001t0004g0020 a0001c0001t0004g0022 others(27): Show |
30 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1452-2282C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763164 | |||||||
chr2:202763167 | G | T | 1 | a0001c0001t0003g0089 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1452-2279G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763167 | |||||||
chr2:202763220 | C | T | 75 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(72): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1452-2226C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763220 | |||||||
chr2:202763309 | T | C | 1 | a0002c0002t0067g0315 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1452-2137T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763309 | |||||||
chr2:202763364 | G | A | 1 | a0001c0001t0008g0189 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1452-2082G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763364 | |||||||
chr2:202764004 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1452-1442G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764004 | |||||||
chr2:202764034 | G | A | 126 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(123): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1452-1412G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764034 | |||||||
chr2:202764128 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1452-1318T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764128 | |||||||
chr2:202764254 | G | A | 9 | a0001c0001t0029g0079 a0001c0001t0029g0268 a0001c0001t0029g0269 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452-1192G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764254 | |||||||
chr2:202764273 | G | T | 1 | a0001c0001t0093g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1452-1173G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764273 | |||||||
chr2:202764328 | G | A | 1 | a0003c0003t0032g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1452-1118G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764328 | |||||||
chr2:202764430 | A | T | 7 | a0001c0001t0002g0068 a0001c0001t0002g0071 a0001c0001t0002g0091 others(4): Show |
7 | HG00408.hp2 HG02071.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-1016A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764430 | |||||||
chr2:202764464 | C | G | 1 | a0001c0001t0025g0213 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452-982C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764464 | |||||||
chr2:202765121 | C | T | 125 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1452-325C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765121 | |||||||
chr2:202765149 | G | A | 1 | a0003c0003t0012g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1452-297G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765149 | |||||||
chr2:202765181 | T | C | 2 | a0001c0001t0107g0266 a0001c0008t0074g0116 |
2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1452-265T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765181 | |||||||
chr2:202765210 | G | A | 1 | a0001c0001t0004g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1452-236G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765210 | |||||||
chr2:202765296 | T | G | 125 | a0001c0001t0001g0114 a0001c0001t0002g0054 a0001c0001t0002g0058 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1452-150T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765296 | |||||||
chr2:202765375 | C | T | 3 | a0001c0001t0107g0266 a0001c0007t0068g0285 a0001c0008t0074g0116 |
3 | HG01884.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1452-71C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765375 | |||||||
chr2:202765379 | C | CT | 11 | a0001c0001t0002g0068 a0001c0001t0002g0071 a0001c0001t0002g0091 others(8): Show |
11 | HG00408.hp2 HG02071.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1452-53dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202765379 | ||||||
chr2:202765387 | T | A | 1 | a0001c0007t0068g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1452-59T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765387 | |||||||
chr2:202765408 | G | T | 1 | a0001c0001t0039g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1452-38G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765408 |