Item | Value |
---|---|
geneid | 166752 |
ensemblid | ENSG00000183090.5 |
hgncid | 25172 |
symbol | FREM3 |
name | FRAS1 related extracellular matrix 3 |
refseq_nuc | NM_001168235.2 |
refseq_prot | NP_001161707.1 |
ensembl_nuc | ENST00000329798.5 |
ensembl_prot | ENSP00000332886.5 |
mane_status | MANE Select |
chr | chr4 |
start | 143577302 |
end | 143700675 |
strand | - |
ver | v1.2 |
region | chr4:143577302-143700675 |
region5000 | chr4:143572302-143705675 |
regionname0 | FREM3_chr4_143577302_143700675 |
regionname5000 | FREM3_chr4_143572302_143705675 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2139 | 124 | 23 | 27 | 47 | 8 | 19 | 35 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0002 | 0/0 | 2139 | 45 | 1 | 16 | 12 | 6 | 10 | 10 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0003 | 0/0 | 2139 | 22 | 7 | 0 | 15 | 0 | 0 | 13 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0004 | 0/0 | 2139 | 13 | 9 | 1 | 3 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0005 | 1/0 | 2139 | 11 | 9 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0006 | 0/0 | 2141 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2136): Show |
chr4 | 143572302 | 143705675 |
a0007 | 0/0 | 2139 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0008 | 0/0 | 2139 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0009 | 0/0 | 2139 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0010 | 0/1 | 2139 | 3 | 0 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0011 | 0/0 | 2139 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0012 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0013 | 0/0 | 2139 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0014 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0015 | 0/0 | 2139 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0016 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0017 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0018 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0019 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0020 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0021 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0022 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0023 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0024 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0025 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0026 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
a0027 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | MAGAS others(2134): Show |
chr4 | 143572302 | 143705675 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 6417 | 116 | 23 | 27 | 39 | 8 | 19 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0001c0006 | 0/0 | 6417 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0001c0028 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0002c0002 | 0/0 | 6417 | 39 | 0 | 13 | 12 | 5 | 9 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0002c0009 | 0/0 | 6417 | 3 | 0 | 3 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0002c0010 | 0/0 | 6417 | 3 | 1 | 0 | 0 | 1 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0003c0003 | 0/0 | 6417 | 22 | 7 | 0 | 15 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0004c0004 | 0/0 | 6417 | 13 | 9 | 1 | 3 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0005c0005 | 0/0 | 6417 | 9 | 8 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0005c0022 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0005c0027 | 1/0 | 6417 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0006c0007 | 0/0 | 6423 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6418): Show |
chr4 | 143572302 | 143705675 | ||
a0007c0008 | 0/0 | 6417 | 5 | 4 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0007c0030 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0008c0011 | 0/0 | 6417 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0009c0013 | 0/0 | 6417 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0010c0015 | 0/0 | 6417 | 2 | 0 | 0 | 0 | 2 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0010c0034 | 0/1 | 6417 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0011c0012 | 0/0 | 6417 | 3 | 3 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0012c0018 | 0/0 | 6417 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0013c0016 | 0/0 | 6417 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0014c0014 | 0/0 | 6417 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0015c0017 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0016c0024 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0017c0025 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0018c0035 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0019c0019 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0020c0026 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0021c0032 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0022c0031 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0023c0029 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0024c0021 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0025c0023 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0026c0033 | 0/0 | 6417 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 | ||
a0027c0020 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6412): Show |
chr4 | 143572302 | 143705675 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6729 | 114 | 21 | 27 | 39 | 8 | 19 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0001c0001t0003 | 0/0 | 6729 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0001c0006t0001 | 0/0 | 6729 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0001c0028t0001 | 0/0 | 6729 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0002c0002t0001 | 0/0 | 6729 | 37 | 0 | 13 | 12 | 5 | 7 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0002c0002t0002 | 0/0 | 6729 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0002c0009t0001 | 0/0 | 6729 | 3 | 0 | 3 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0002c0010t0001 | 0/0 | 6729 | 3 | 1 | 0 | 0 | 1 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0003c0003t0001 | 0/0 | 6729 | 22 | 7 | 0 | 15 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0004c0004t0001 | 0/0 | 6729 | 13 | 9 | 1 | 3 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0005c0005t0001 | 0/0 | 6729 | 9 | 8 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0005c0022t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0005c0027t0001 | 1/0 | 6729 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0006c0007t0001 | 0/0 | 6735 | 7 | 0 | 0 | 7 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6730): Show |
chr4 | 143572302 | 143705675 |
a0007c0008t0001 | 0/0 | 6729 | 5 | 4 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0007c0030t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0008c0011t0001 | 0/0 | 6729 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0009c0013t0001 | 0/0 | 6729 | 3 | 2 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0010c0015t0001 | 0/0 | 6729 | 2 | 0 | 0 | 0 | 2 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0010c0034t0001 | 0/1 | 6729 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0011c0012t0001 | 0/0 | 6729 | 3 | 3 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0012c0018t0001 | 0/0 | 6729 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0013c0016t0001 | 0/0 | 6729 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0014c0014t0001 | 0/0 | 6729 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0015c0017t0001 | 0/0 | 6729 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0016c0024t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0017c0025t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0018c0035t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0019c0019t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0020c0026t0001 | 0/0 | 6729 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0021c0032t0004 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0022c0031t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0023c0029t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0024c0021t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0025c0023t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0026c0033t0001 | 0/0 | 6729 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
a0027c0020t0001 | 0/0 | 6729 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | ATGGC others(6724): Show |
chr4 | 143572302 | 143705675 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0001c0028t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0009t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0009t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0009t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0010t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0010t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0002c0010t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0003c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0004c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0022t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0005c0027t0001g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0006c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0008t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0008t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0008t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0007c0030t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0008c0011t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0008c0011t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0009c0013t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0009c0013t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0010c0015t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0010c0015t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0010c0034t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0011c0012t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0011c0012t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0012c0018t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0012c0018t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0013c0016t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0013c0016t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0014c0014t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0014c0014t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0015c0017t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0015c0017t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0016c0024t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0017c0025t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0018c0035t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0019c0019t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0020c0026t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0021c0032t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0022c0031t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0023c0029t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0024c0021t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0025c0023t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0026c0033t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
a0027c0020t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0034 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | FIN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0088 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0078 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0085 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01069 | hp1 | a0002 | c0009 | t0001 | g0013 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01070 | hp2 | a0012 | c0018 | t0001 | g0243 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01071 | hp1 | a0002 | c0009 | t0001 | g0012 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01071 | hp2 | a0012 | c0018 | t0001 | g0244 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01099 | hp2 | a0013 | c0016 | t0001 | g0073 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01106 | hp1 | a0005 | c0005 | t0001 | g0060 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01168 | hp1 | a0002 | c0009 | t0001 | g0011 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01192 | hp1 | a0008 | c0011 | t0001 | g0066 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01243 | hp1 | a0016 | c0024 | t0001 | g0069 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01243 | hp2 | a0009 | c0013 | t0001 | g0008 | AMR | PUR | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01261 | hp2 | a0007 | c0008 | t0001 | g0156 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01361 | hp2 | a0017 | c0025 | t0001 | g0070 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01496 | hp2 | a0004 | c0004 | t0001 | g0097 | AMR | CLM | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01515 | hp1 | a0010 | c0015 | t0001 | g0071 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01517 | hp2 | a0010 | c0015 | t0001 | g0072 | EUR | IBS | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01884 | hp1 | a0018 | c0035 | t0001 | g0245 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0101 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01891 | hp1 | a0011 | c0012 | t0001 | g0068 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01943 | hp2 | a0019 | c0019 | t0001 | g0010 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01975 | hp2 | a0013 | c0016 | t0001 | g0074 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02004 | hp2 | a0020 | c0026 | t0001 | g0076 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02055 | hp1 | a0004 | c0004 | t0001 | g0096 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02055 | hp2 | a0005 | c0005 | t0001 | g0064 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02132 | hp1 | a0004 | c0004 | t0001 | g0079 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02132 | hp2 | a0006 | c0007 | t0001 | g0251 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02165 | hp2 | a0001 | c0028 | t0001 | g0110 | EAS | CDX | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02280 | hp1 | a0021 | c0032 | t0004 | g0152 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02451 | hp1 | a0007 | c0008 | t0001 | g0147 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02451 | hp2 | a0004 | c0004 | t0001 | g0102 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02572 | hp2 | a0005 | c0005 | t0001 | g0061 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02622 | hp1 | a0005 | c0005 | t0001 | g0058 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02622 | hp2 | a0007 | c0030 | t0001 | g0153 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02630 | hp1 | a0005 | c0022 | t0001 | g0065 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02647 | hp2 | a0005 | c0005 | t0001 | g0056 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02717 | hp1 | a0005 | c0005 | t0001 | g0059 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02922 | hp2 | a0022 | c0031 | t0001 | g0145 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02965 | hp1 | a0005 | c0005 | t0001 | g0062 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02970 | hp1 | a0011 | c0012 | t0001 | g0004 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02970 | hp2 | a0009 | c0013 | t0001 | g0246 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02976 | hp2 | a0004 | c0004 | t0001 | g0098 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03041 | hp1 | a0004 | c0004 | t0001 | g0090 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0107 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0108 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03098 | hp2 | a0007 | c0008 | t0001 | g0136 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03130 | hp1 | a0023 | c0029 | t0001 | g0231 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03130 | hp2 | a0004 | c0004 | t0001 | g0092 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03195 | hp1 | a0024 | c0021 | t0001 | g0055 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | ESN | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03209 | hp1 | a0009 | c0013 | t0001 | g0008 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03225 | hp2 | a0014 | c0014 | t0001 | g0052 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03453 | hp1 | a0025 | c0023 | t0001 | g0067 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03453 | hp2 | a0014 | c0014 | t0001 | g0053 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0057 | AFR | GWD | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03579 | hp1 | a0008 | c0011 | t0001 | g0003 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0091 | AFR | MSL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03710 | hp2 | a0002 | c0010 | t0001 | g0015 | SAS | PJL | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0036 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG03834 | hp2 | a0026 | c0033 | t0001 | g0241 | SAS | BEB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18522 | hp1 | a0004 | c0004 | t0001 | g0100 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18612 | hp2 | a0015 | c0017 | t0001 | g0172 | EAS | CHB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18906 | hp1 | a0004 | c0004 | t0001 | g0093 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0063 | AFR | YRI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18943 | hp2 | a0006 | c0007 | t0001 | g0009 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18946 | hp1 | a0001 | c0006 | t0001 | g0112 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18951 | hp1 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18953 | hp2 | a0001 | c0006 | t0001 | g0111 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18957 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18975 | hp2 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18978 | hp2 | a0006 | c0007 | t0001 | g0250 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18979 | hp2 | a0004 | c0004 | t0001 | g0105 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18986 | hp2 | a0015 | c0017 | t0001 | g0207 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18987 | hp1 | a0001 | c0006 | t0001 | g0113 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0087 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19010 | hp1 | a0006 | c0007 | t0001 | g0248 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19011 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19030 | hp2 | a0027 | c0020 | t0001 | g0054 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19065 | hp2 | a0001 | c0006 | t0001 | g0114 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19079 | hp1 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19082 | hp2 | a0006 | c0007 | t0001 | g0249 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19084 | hp1 | a0006 | c0007 | t0001 | g0009 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19089 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA19089 | hp2 | a0006 | c0007 | t0001 | g0247 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0099 | AFR | ASW | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20129 | hp2 | a0008 | c0011 | t0001 | g0003 | AFR | ASW | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20805 | hp1 | a0002 | c0010 | t0001 | g0014 | EUR | TSI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02109 | hp1 | a0011 | c0012 | t0001 | g0004 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02486 | hp1 | a0007 | c0008 | t0001 | g0238 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02559 | hp1 | a0002 | c0010 | t0001 | g0016 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
HG06807 | hp2 | a0007 | c0008 | t0001 | g0144 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18955 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0094 | AFR | USA | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
homoSapiens | chm13v2 | a0010 | c0034 | t0001 | g0242 | REF | REF | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
homoSapiens | grch38p0 | a0005 | c0027 | t0001 | g0109 | REF | REF | FREM3_chr4_143572302_143705675 | FREM3 | chr4 | 143572302 | 143705675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143577615 | T | C | 2 | a0009 a0022 |
4 | HG01243.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.6416A>G | p.Asp2139Gly | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6416/6729 | 6416/6420 | 2139/2139 | chr4 | 143577615 | |||
chr4:143577712 | T | A | 1 | a0021 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.6319A>T | p.Met2107Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6319/6729 | 6319/6420 | 2107/2139 | chr4 | 143577712 | |||
chr4:143577729 | A | G | 1 | a0015 | 2 | NA18612.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.6302T>C | p.Phe2101Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6302/6729 | 6302/6420 | 2101/2139 | chr4 | 143577729 | |||
chr4:143585880 | C | T | 1 | a0011 | 3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.6142G>A | p.Val2048Met | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/8 | 6142/6729 | 6142/6420 | 2048/2139 | chr4 | 143585880 | |||
chr4:143611458 | G | T | 1 | a0020 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.5849C>A | p.Thr1950Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/8 | 5849/6729 | 5849/6420 | 1950/2139 | chr4 | 143611458 | |||
chr4:143611491 | A | G | 3 | a0004 a0023 a0025 |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
missense_variant | MODERATE | c.5816T>C | p.Phe1939Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/8 | 5816/6729 | 5816/6420 | 1939/2139 | chr4 | 143611491 | |||
chr4:143621060 | A | G | 6 | a0004 a0007 a0008 others(3): Show |
26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
missense_variant | MODERATE | c.5756T>C | p.Ile1919Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/8 | 5756/6729 | 5756/6420 | 1919/2139 | chr4 | 143621060 | |||
chr4:143695685 | G | C | 1 | a0026 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.4991C>G | p.Thr1664Ser | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4991/6729 | 4991/6420 | 1664/2139 | chr4 | 143695685 | |||
chr4:143696163 | C | T | 2 | a0011 a0016 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.4513G>A | p.Glu1505Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4513/6729 | 4513/6420 | 1505/2139 | chr4 | 143696163 | |||
chr4:143696194 | G | C | 2 | a0011 a0016 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.4482C>G | p.Asn1494Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4482/6729 | 4482/6420 | 1494/2139 | chr4 | 143696194 | |||
chr4:143696244 | A | T | 4 | a0003 a0004 a0013 others(1): Show |
38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
missense_variant | MODERATE | c.4432T>A | p.Tyr1478Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4432/6729 | 4432/6420 | 1478/2139 | chr4 | 143696244 | |||
chr4:143696966 | C | T | 1 | a0013 | 2 | HG01099.hp2 HG01975.hp2 |
missense_variant | MODERATE | c.3710G>A | p.Arg1237Gln | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3710/6729 | 3710/6420 | 1237/2139 | chr4 | 143696966 | |||
chr4:143697191 | T | C | 1 | a0024 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.3485A>G | p.Gln1162Arg | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3485/6729 | 3485/6420 | 1162/2139 | chr4 | 143697191 | |||
chr4:143697457 | G | C | 26 | a0001 a0002 a0003 others(23): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
missense_variant | MODERATE | c.3219C>G | p.Phe1073Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3219/6729 | 3219/6420 | 1073/2139 | chr4 | 143697457 | |||
chr4:143697935 | G | T | 2 | a0011 a0016 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
missense_variant | MODERATE | c.2741C>A | p.Thr914Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2741/6729 | 2741/6420 | 914/2139 | chr4 | 143697935 | |||
chr4:143698161 | T | G | 1 | a0010 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.2515A>C | p.Ile839Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2515/6729 | 2515/6420 | 839/2139 | chr4 | 143698161 | |||
chr4:143699177 | G | T | 1 | a0019 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1499C>A | p.Ala500Glu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1499/6729 | 1499/6420 | 500/2139 | chr4 | 143699177 | |||
chr4:143699189 | G | A | 3 | a0009 a0012 a0018 |
6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
missense_variant | MODERATE | c.1487C>T | p.Ala496Val | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1487/6729 | 1487/6420 | 496/2139 | chr4 | 143699189 | |||
chr4:143699290 | T | G | 2 | a0008 a0025 |
4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.1386A>C | p.Lys462Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1386/6729 | 1386/6420 | 462/2139 | chr4 | 143699290 | |||
chr4:143699849 | C | T | 1 | a0027 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.827G>A | p.Gly276Asp | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 827/6729 | 827/6420 | 276/2139 | chr4 | 143699849 | |||
chr4:143699853 | C | T | 1 | a0017 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.823G>A | p.Glu275Lys | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 823/6729 | 823/6420 | 275/2139 | chr4 | 143699853 | |||
chr4:143700104 | C | G | 1 | a0014 | 2 | HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.572G>C | p.Arg191Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 572/6729 | 572/6420 | 191/2139 | chr4 | 143700104 | |||
chr4:143700251 | T | TGCAGCA | 1 | a0006 | 7 | HG02132.hp2 NA18943.hp2 NA18978.hp2 others(4): Show |
conservative_inframe_insertion | MODERATE | c.419_424dupTGCTGC | p.Leu140_Leu141dup | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 424/6729 | 424/6420 | 142/2139 | chr4 | 143700251 | |||
chr4:143700626 | A | G | 2 | a0002 a0019 |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
missense_variant | MODERATE | c.50T>C | p.Val17Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 50/6729 | 50/6420 | 17/2139 | chr4 | 143700626 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143577647 | C | T | 1 | a0021c0032 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.6384G>A | p.Thr2128Thr | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 6384/6729 | 6384/6420 | 2128/2139 | chr4 | 143577647 | |||
chr4:143585881 | G | A | 1 | a0007c0030 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.6141C>T | p.Ala2047Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/8 | 6141/6729 | 6141/6420 | 2047/2139 | chr4 | 143585881 | |||
chr4:143695753 | C | T | 1 | a0002c0010 | 3 | HG02559.hp1 HG03710.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.4923G>A | p.Ala1641Ala | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4923/6729 | 4923/6420 | 1641/2139 | chr4 | 143695753 | |||
chr4:143696401 | G | T | 1 | a0002c0009 | 3 | HG01069.hp1 HG01071.hp1 HG01168.hp1 |
synonymous_variant | LOW | c.4275C>A | p.Val1425Val | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 4275/6729 | 4275/6420 | 1425/2139 | chr4 | 143696401 | |||
chr4:143696689 | G | T | 13 | a0001c0006 a0002c0002 a0002c0009 others(10): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
synonymous_variant | LOW | c.3987C>A | p.Ile1329Ile | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3987/6729 | 3987/6420 | 1329/2139 | chr4 | 143696689 | |||
chr4:143697448 | C | T | 1 | a0001c0028 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.3228G>A | p.Glu1076Glu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 3228/6729 | 3228/6420 | 1076/2139 | chr4 | 143697448 | |||
chr4:143697927 | G | A | 1 | a0005c0022 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2749C>T | p.Leu917Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2749/6729 | 2749/6420 | 917/2139 | chr4 | 143697927 | |||
chr4:143698135 | G | A | 2 | a0005c0005 a0005c0022 |
10 | HG01106.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
synonymous_variant | LOW | c.2541C>T | p.Leu847Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2541/6729 | 2541/6420 | 847/2139 | chr4 | 143698135 | |||
chr4:143698624 | A | G | 1 | a0024c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2052T>C | p.Asn684Asn | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 2052/6729 | 2052/6420 | 684/2139 | chr4 | 143698624 | |||
chr4:143698768 | C | T | 4 | a0003c0003 a0004c0004 a0013c0016 others(1): Show |
38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
synonymous_variant | LOW | c.1908G>A | p.Gly636Gly | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1908/6729 | 1908/6420 | 636/2139 | chr4 | 143698768 | |||
chr4:143698981 | A | G | 1 | a0010c0015 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.1695T>C | p.Phe565Phe | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1695/6729 | 1695/6420 | 565/2139 | chr4 | 143698981 | |||
chr4:143699605 | C | T | 12 | a0002c0002 a0002c0009 a0002c0010 others(9): Show |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
synonymous_variant | LOW | c.1071G>A | p.Pro357Pro | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 1071/6729 | 1071/6420 | 357/2139 | chr4 | 143699605 | |||
chr4:143699755 | G | A | 2 | a0011c0012 a0016c0024 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
synonymous_variant | LOW | c.921C>T | p.Pro307Pro | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 921/6729 | 921/6420 | 307/2139 | chr4 | 143699755 | |||
chr4:143700046 | A | G | 12 | a0002c0002 a0002c0009 a0002c0010 others(9): Show |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
synonymous_variant | LOW | c.630T>C | p.Leu210Leu | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/8 | 630/6729 | 630/6420 | 210/2139 | chr4 | 143700046 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143577319 | T | C | 1 | a0021c0032t0004 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 292 | chr4 | 143577319 | ||||||
chr4:143577522 | T | C | 1 | a0001c0001t0003 | 2 | HG02559.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 89 | chr4 | 143577522 | ||||||
chr4:143577538 | A | T | 1 | a0002c0002t0002 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 8/8 | 73 | chr4 | 143577538 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143577859 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.6179-7T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143577859 | |||||||
chr4:143577910 | C | T | 4 | a0004c0004t0001g0092 a0007c0030t0001g0153 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-58G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143577910 | |||||||
chr4:143578133 | A | T | 117 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0123 others(114): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.6179-281T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143578133 | |||||||
chr4:143578691 | A | G | 93 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0125 others(90): Show |
97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.6179-839T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143578691 | |||||||
chr4:143579015 | T | C | 1 | a0004c0004t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6179-1163A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579015 | |||||||
chr4:143579043 | AC | A | 4 | a0004c0004t0001g0092 a0007c0030t0001g0153 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-1192delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579043 | |||||||
chr4:143579047 | A | T | 4 | a0004c0004t0001g0092 a0007c0030t0001g0153 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.6179-1195T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579047 | |||||||
chr4:143579062 | CA | C | 5 | a0001c0001t0003g0232 a0001c0001t0003g0233 a0007c0030t0001g0153 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.6179-1211delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579062 | |||||||
chr4:143579078 | C | T | 130 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(127): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.6179-1226G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579078 | |||||||
chr4:143579703 | G | A | 2 | a0003c0003t0001g0107 a0004c0004t0001g0099 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.6179-1851C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579703 | |||||||
chr4:143579737 | T | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-1885A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579737 | |||||||
chr4:143579753 | C | T | 246 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6179-1901G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579753 | |||||||
chr4:143579801 | G | A | 1 | a0014c0014t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6179-1949C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579801 | |||||||
chr4:143579943 | C | T | 3 | a0001c0001t0001g0120 a0002c0002t0001g0017 a0002c0002t0001g0019 |
3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6179-2091G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143579943 | |||||||
chr4:143580053 | T | G | 47 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0122 others(44): Show |
51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-2201A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580053 | |||||||
chr4:143580063 | C | T | 1 | a0003c0003t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6179-2211G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580063 | |||||||
chr4:143580111 | A | C | 2 | a0010c0015t0001g0071 a0010c0015t0001g0072 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6179-2259T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580111 | |||||||
chr4:143580148 | T | C | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.6179-2296A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580148 | |||||||
chr4:143580707 | C | G | 196 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(193): Show |
201 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.6179-2855G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580707 | |||||||
chr4:143580711 | C | A | 3 | a0004c0004t0001g0090 a0023c0029t0001g0231 a0026c0033t0001g0241 |
3 | HG03041.hp1 HG03130.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.6179-2859G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580711 | |||||||
chr4:143580932 | G | A | 47 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0122 others(44): Show |
51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-3080C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143580932 | |||||||
chr4:143581007 | A | G | 47 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0122 others(44): Show |
51 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.6179-3155T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581007 | |||||||
chr4:143581047 | A | G | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.6179-3195T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581047 | |||||||
chr4:143581124 | A | C | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.6179-3272T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581124 | |||||||
chr4:143581326 | C | T | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6179-3474G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581326 | |||||||
chr4:143581329 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6179-3477G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581329 | |||||||
chr4:143581387 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.6179-3535G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581387 | |||||||
chr4:143581498 | C | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6179-3646G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581498 | |||||||
chr4:143581636 | T | C | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-3784A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581636 | |||||||
chr4:143581675 | A | C | 1 | a0002c0002t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6179-3823T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581675 | |||||||
chr4:143581828 | C | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6179-3976G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581828 | |||||||
chr4:143581933 | AC | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0192 |
3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6178+3910delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143581933 | |||||||
chr4:143582114 | CA | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(13): Show |
17 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.6178+3729delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582114 | |||||||
chr4:143582118 | A | G | 1 | a0003c0003t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3726T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582118 | |||||||
chr4:143582119 | G | C | 1 | a0003c0003t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3725C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582119 | |||||||
chr4:143582444 | A | G | 1 | a0003c0003t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+3400T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582444 | |||||||
chr4:143582494 | G | A | 63 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0151 others(60): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.6178+3350C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582494 | |||||||
chr4:143582577 | C | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6178+3267G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582577 | |||||||
chr4:143582748 | A | G | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6178+3096T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582748 | |||||||
chr4:143582839 | A | C | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.6178+3005T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582839 | |||||||
chr4:143582898 | C | CT | 212 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(209): Show |
219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.6178+2945dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582898 | |||||||
chr4:143582915 | T | C | 245 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(242): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6178+2929A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143582915 | |||||||
chr4:143583041 | G | T | 245 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(242): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.6178+2803C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583041 | |||||||
chr4:143583042 | G | T | 1 | a0003c0003t0001g0080 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6178+2802C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583042 | |||||||
chr4:143583062 | T | C | 36 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0159 others(33): Show |
39 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.6178+2782A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583062 | |||||||
chr4:143583130 | A | G | 1 | a0026c0033t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6178+2714T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583130 | |||||||
chr4:143583163 | C | T | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6178+2681G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583163 | |||||||
chr4:143583164 | G | A | 3 | a0001c0001t0001g0121 a0002c0002t0002g0002 a0003c0003t0001g0081 |
4 | HG02976.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.6178+2680C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583164 | |||||||
chr4:143583300 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0218 |
2 | HG02738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.6178+2544G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583300 | |||||||
chr4:143583326 | A | G | 3 | a0008c0011t0001g0066 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6178+2518T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583326 | |||||||
chr4:143583364 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6178+2480G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583364 | |||||||
chr4:143583409 | T | A | 64 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0151 others(61): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.6178+2435A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583409 | |||||||
chr4:143583439 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6178+2405T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583439 | |||||||
chr4:143583453 | C | T | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+2391G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583453 | |||||||
chr4:143583454 | A | G | 132 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0122 others(129): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.6178+2390T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583454 | |||||||
chr4:143583465 | T | C | 246 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6178+2379A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583465 | |||||||
chr4:143583653 | A | C | 1 | a0002c0002t0001g0051 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6178+2191T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583653 | |||||||
chr4:143583918 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6178+1926G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583918 | |||||||
chr4:143583996 | T | C | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6178+1848A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143583996 | |||||||
chr4:143584136 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6178+1708C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584136 | |||||||
chr4:143584205 | C | T | 2 | a0001c0001t0001g0154 a0003c0003t0001g0083 |
2 | NA18941.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6178+1639G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584205 | |||||||
chr4:143584266 | G | A | 3 | a0008c0011t0001g0066 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6178+1578C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584266 | |||||||
chr4:143584272 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+1572C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584272 | |||||||
chr4:143584353 | A | G | 246 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6178+1491T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584353 | |||||||
chr4:143584373 | C | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0198 a0005c0005t0001g0059 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.6178+1471G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584373 | |||||||
chr4:143584379 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6178+1465C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584379 | |||||||
chr4:143584383 | T | A | 1 | a0003c0003t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6178+1461A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584383 | |||||||
chr4:143584395 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+1449C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584395 | |||||||
chr4:143584415 | CA | C | 82 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(79): Show |
82 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.6178+1428delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584415 | |||||||
chr4:143584415 | CAA | C | 119 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0122 others(116): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.6178+1427_6178+142 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584415 | |||||||
chr4:143584492 | C | T | 1 | a0004c0004t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6178+1352G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584492 | |||||||
chr4:143584540 | T | C | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.6178+1304A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584540 | |||||||
chr4:143584620 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.6178+1224T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584620 | |||||||
chr4:143584922 | C | A | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6178+922G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143584922 | |||||||
chr4:143585201 | A | C | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+643T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585201 | |||||||
chr4:143585257 | G | T | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.6178+587C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585257 | |||||||
chr4:143585276 | C | T | 1 | a0004c0004t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6178+568G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585276 | |||||||
chr4:143585282 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6178+562C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585282 | |||||||
chr4:143585510 | G | A | 4 | a0002c0002t0001g0018 a0002c0002t0001g0025 a0002c0009t0001g0012 others(1): Show |
4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.6178+334C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585510 | |||||||
chr4:143585561 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6178+283G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 7/7 | chr4 | 143585561 | |||||||
chr4:143586117 | G | GT | 74 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(71): Show |
74 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.6029-125dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586117 | |||||||
chr4:143586553 | G | A | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-560C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586553 | |||||||
chr4:143586557 | A | G | 65 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0131 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-564T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143586557 | |||||||
chr4:143587107 | A | G | 1 | a0002c0010t0001g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6029-1114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587107 | |||||||
chr4:143587235 | A | AT | 31 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-1243dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587235 | |||||||
chr4:143587247 | C | T | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-1254G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587247 | |||||||
chr4:143587292 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-1299G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587292 | |||||||
chr4:143587375 | A | G | 1 | a0004c0004t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-1382T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587375 | |||||||
chr4:143587384 | C | T | 107 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(104): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-1391G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587384 | |||||||
chr4:143587401 | G | A | 137 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6029-1408C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587401 | |||||||
chr4:143587426 | G | A | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0132 others(2): Show |
5 | HG00673.hp2 NA18973.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-1433C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587426 | |||||||
chr4:143587435 | T | C | 107 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(104): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-1442A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587435 | |||||||
chr4:143587655 | C | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6029-1662G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587655 | |||||||
chr4:143587749 | C | T | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-1756G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587749 | |||||||
chr4:143587763 | G | GA | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-1771_6029-177 others(5): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587763 | |||||||
chr4:143587854 | C | T | 1 | a0021c0032t0004g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6029-1861G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143587854 | |||||||
chr4:143588148 | G | T | 1 | a0006c0007t0001g0251 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6029-2155C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588148 | |||||||
chr4:143588239 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-2246C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588239 | |||||||
chr4:143588249 | T | A | 2 | a0003c0003t0001g0075 a0003c0003t0001g0087 |
2 | NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.6029-2256A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588249 | |||||||
chr4:143588359 | C | A | 1 | a0004c0004t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6029-2366G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588359 | |||||||
chr4:143588576 | T | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(64): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.6029-2583A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588576 | |||||||
chr4:143588599 | C | T | 23 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.6029-2606G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588599 | |||||||
chr4:143588609 | T | G | 1 | a0002c0002t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6029-2616A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588609 | |||||||
chr4:143588705 | C | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-2712G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588705 | |||||||
chr4:143588740 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.6029-2747A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588740 | |||||||
chr4:143588812 | T | A | 136 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(133): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.6029-2819A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588812 | |||||||
chr4:143588812 | T | C | 106 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(103): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6029-2819A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588812 | |||||||
chr4:143588816 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6029-2823G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588816 | |||||||
chr4:143588864 | G | T | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-2871C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588864 | |||||||
chr4:143588870 | A | G | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-2877T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588870 | |||||||
chr4:143588888 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6029-2895G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588888 | |||||||
chr4:143588896 | C | T | 1 | a0026c0033t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6029-2903G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588896 | |||||||
chr4:143588906 | T | A | 106 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(103): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6029-2913A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588906 | |||||||
chr4:143588907 | C | T | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-2914G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588907 | |||||||
chr4:143588929 | C | T | 4 | a0002c0002t0001g0031 a0009c0013t0001g0008 a0009c0013t0001g0246 others(1): Show |
5 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-2936G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588929 | |||||||
chr4:143588930 | A | G | 4 | a0002c0002t0001g0031 a0009c0013t0001g0008 a0009c0013t0001g0246 others(1): Show |
5 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-2937T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143588930 | |||||||
chr4:143589162 | T | G | 1 | a0009c0013t0001g0246 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6029-3169A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589162 | |||||||
chr4:143589175 | G | T | 1 | a0002c0002t0001g0032 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.6029-3182C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589175 | |||||||
chr4:143589268 | G | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3275C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589268 | |||||||
chr4:143589332 | T | C | 1 | a0002c0002t0001g0050 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6029-3339A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589332 | |||||||
chr4:143589334 | G | A | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3341C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589334 | |||||||
chr4:143589339 | G | C | 67 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(64): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.6029-3346C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589339 | |||||||
chr4:143589383 | G | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0225 |
2 | HG00741.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.6029-3390C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589383 | |||||||
chr4:143589384 | TA | T | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3392delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589384 | |||||||
chr4:143589438 | C | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-3445G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589438 | |||||||
chr4:143589522 | C | G | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-3529G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589522 | |||||||
chr4:143589580 | C | G | 76 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(73): Show |
76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.6029-3587G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589580 | |||||||
chr4:143589686 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6029-3693G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589686 | |||||||
chr4:143589707 | T | A | 25 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0131 others(22): Show |
26 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.6029-3714A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589707 | |||||||
chr4:143589717 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3724C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589717 | |||||||
chr4:143589721 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(211): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.6029-3728A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589721 | |||||||
chr4:143589769 | T | G | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-3776A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589769 | |||||||
chr4:143589848 | C | A | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-3855G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589848 | |||||||
chr4:143589957 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0003c0003t0001g0103 |
3 | HG02257.hp2 HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6029-3964G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143589957 | |||||||
chr4:143590011 | C | T | 217 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(214): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.6029-4018G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590011 | |||||||
chr4:143590023 | C | T | 136 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(133): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.6029-4030G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590023 | |||||||
chr4:143590145 | G | A | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-4152C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590145 | |||||||
chr4:143590246 | C | T | 1 | a0003c0003t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6029-4253G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590246 | |||||||
chr4:143590265 | C | T | 2 | a0001c0001t0001g0198 a0005c0005t0001g0059 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6029-4272G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590265 | |||||||
chr4:143590281 | A | G | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-4288T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590281 | |||||||
chr4:143590332 | G | A | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-4339C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590332 | |||||||
chr4:143590333 | T | C | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-4340A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590333 | |||||||
chr4:143590376 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6029-4383C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590376 | |||||||
chr4:143590496 | C | G | 67 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(64): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.6029-4503G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590496 | |||||||
chr4:143590509 | T | C | 3 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0008c0011t0001g0003 |
4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6029-4516A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590509 | |||||||
chr4:143590664 | A | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-4671T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590664 | |||||||
chr4:143590682 | T | C | 3 | a0008c0011t0001g0066 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.6029-4689A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590682 | |||||||
chr4:143590692 | A | G | 1 | a0004c0004t0001g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.6029-4699T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590692 | |||||||
chr4:143590721 | A | C | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-4728T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590721 | |||||||
chr4:143590723 | G | C | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-4730C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590723 | |||||||
chr4:143590795 | A | G | 68 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0131 others(65): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.6029-4802T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590795 | |||||||
chr4:143590808 | A | G | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-4815T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590808 | |||||||
chr4:143590847 | G | A | 5 | a0001c0001t0001g0169 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01257.hp1 HG01496.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-4854C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590847 | |||||||
chr4:143590995 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6029-5002T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143590995 | |||||||
chr4:143591098 | T | G | 107 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(104): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-5105A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591098 | |||||||
chr4:143591123 | C | G | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6029-5130G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591123 | |||||||
chr4:143591278 | C | T | 1 | a0002c0002t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6029-5285G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591278 | |||||||
chr4:143591290 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6029-5297A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591290 | |||||||
chr4:143591545 | C | T | 5 | a0001c0001t0001g0169 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01257.hp1 HG01496.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-5552G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591545 | |||||||
chr4:143591546 | G | A | 137 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6029-5553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591546 | |||||||
chr4:143591635 | T | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0162 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.6029-5642A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591635 | |||||||
chr4:143591637 | T | G | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.6029-5644A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591637 | |||||||
chr4:143591751 | G | T | 79 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(76): Show |
79 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.6029-5758C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591751 | |||||||
chr4:143591813 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(213): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.6029-5820G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591813 | |||||||
chr4:143591836 | C | T | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-5843G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591836 | |||||||
chr4:143591855 | T | G | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-5862A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591855 | |||||||
chr4:143591895 | A | C | 67 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(64): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.6029-5902T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591895 | |||||||
chr4:143591918 | A | G | 1 | a0026c0033t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6029-5925T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591918 | |||||||
chr4:143591966 | G | A | 1 | a0004c0004t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-5973C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143591966 | |||||||
chr4:143592037 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6029-6044C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592037 | |||||||
chr4:143592236 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0225 a0001c0001t0001g0227 |
3 | HG00673.hp1 NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.6029-6243A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592236 | |||||||
chr4:143592348 | C | CAATTTGG others(1412): Show |
2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-6356_6029-635 others(1423): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592348 | |||||||
chr4:143592436 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.6029-6443C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592436 | |||||||
chr4:143592441 | G | A | 65 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0131 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-6448C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592441 | |||||||
chr4:143592441 | G | C | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-6448C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592441 | |||||||
chr4:143592445 | A | G | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6029-6452T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592445 | |||||||
chr4:143592519 | T | G | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6526A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592519 | |||||||
chr4:143592565 | G | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-6572C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592565 | |||||||
chr4:143592566 | G | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(64): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.6029-6573C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592566 | |||||||
chr4:143592567 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6029-6574G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592567 | |||||||
chr4:143592610 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6029-6617C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592610 | |||||||
chr4:143592613 | G | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6620C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592613 | |||||||
chr4:143592626 | G | C | 31 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-6633C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592626 | |||||||
chr4:143592647 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6029-6654C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592647 | |||||||
chr4:143592822 | C | T | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-6829G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592822 | |||||||
chr4:143592824 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6029-6831A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592824 | |||||||
chr4:143592858 | C | A | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-6865G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592858 | |||||||
chr4:143592859 | G | A | 6 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0008c0011t0001g0003 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.6029-6866C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592859 | |||||||
chr4:143592934 | G | A | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-6941C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592934 | |||||||
chr4:143592997 | C | G | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-7004G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143592997 | |||||||
chr4:143593000 | C | T | 74 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(71): Show |
74 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.6029-7007G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593000 | |||||||
chr4:143593031 | C | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-7038G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593031 | |||||||
chr4:143593064 | C | T | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-7071G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593064 | |||||||
chr4:143593065 | G | A | 65 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0131 others(62): Show |
66 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.6029-7072C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593065 | |||||||
chr4:143593177 | C | T | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-7184G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593177 | |||||||
chr4:143593187 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6029-7194G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593187 | |||||||
chr4:143593213 | T | C | 2 | a0002c0009t0001g0012 a0002c0009t0001g0013 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.6029-7220A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593213 | |||||||
chr4:143593267 | G | A | 134 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(131): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.6029-7274C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593267 | |||||||
chr4:143593301 | G | A | 6 | a0003c0003t0001g0101 a0005c0005t0001g0063 a0005c0022t0001g0065 others(3): Show |
6 | HG01261.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.6029-7308C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593301 | |||||||
chr4:143593359 | T | A | 1 | a0022c0031t0001g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6029-7366A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593359 | |||||||
chr4:143593396 | C | T | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-7403G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593396 | |||||||
chr4:143593456 | C | T | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7463G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593456 | |||||||
chr4:143593532 | G | A | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-7539C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593532 | |||||||
chr4:143593549 | G | A | 31 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-7556C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593549 | |||||||
chr4:143593584 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-7591C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593584 | |||||||
chr4:143593646 | C | G | 1 | a0002c0002t0001g0050 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6029-7653G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593646 | |||||||
chr4:143593675 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7682C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593675 | |||||||
chr4:143593693 | T | A | 134 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(131): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.6029-7700A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593693 | |||||||
chr4:143593702 | A | C | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-7709T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593702 | |||||||
chr4:143593736 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0223 |
3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6029-7743C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143593736 | |||||||
chr4:143594016 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6029-8023T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594016 | |||||||
chr4:143594033 | C | T | 2 | a0011c0012t0001g0004 a0011c0012t0001g0068 |
3 | HG01891.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6029-8040G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594033 | |||||||
chr4:143594063 | G | T | 76 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(73): Show |
76 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.6029-8070C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594063 | |||||||
chr4:143594210 | C | G | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-8217G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594210 | |||||||
chr4:143594211 | A | G | 31 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.6029-8218T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594211 | |||||||
chr4:143594214 | C | T | 1 | a0002c0002t0001g0032 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.6029-8221G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594214 | |||||||
chr4:143594215 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6029-8222C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594215 | |||||||
chr4:143594304 | C | T | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-8311G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594304 | |||||||
chr4:143594354 | T | A | 137 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0121 others(134): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6029-8361A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594354 | |||||||
chr4:143594381 | C | T | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0119 others(70): Show |
73 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-8388G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594381 | |||||||
chr4:143594447 | A | G | 1 | a0013c0016t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6029-8454T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594447 | |||||||
chr4:143594480 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-8487T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594480 | |||||||
chr4:143594480 | A | T | 6 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0008c0011t0001g0003 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.6029-8487T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594480 | |||||||
chr4:143594611 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6029-8618G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594611 | |||||||
chr4:143594661 | G | A | 246 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(243): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6029-8668C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594661 | |||||||
chr4:143594710 | C | G | 1 | a0004c0004t0001g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6029-8717G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594710 | |||||||
chr4:143594735 | G | A | 107 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(104): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6029-8742C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594735 | |||||||
chr4:143594743 | A | C | 34 | a0001c0001t0001g0118 a0001c0001t0001g0159 a0001c0001t0001g0160 others(31): Show |
36 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.6029-8750T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143594743 | |||||||
chr4:143595009 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6029-9016C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595009 | |||||||
chr4:143595430 | G | A | 1 | a0007c0008t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6029-9437C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595430 | |||||||
chr4:143595438 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0192 |
3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.6029-9445T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595438 | |||||||
chr4:143595468 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0167 |
2 | HG00738.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.6029-9475C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595468 | |||||||
chr4:143595470 | G | C | 3 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0008c0011t0001g0003 |
4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6029-9477C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595470 | |||||||
chr4:143595637 | C | T | 152 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(149): Show |
158 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.6029-9644G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595637 | |||||||
chr4:143595662 | C | T | 137 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(134): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.6029-9669G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595662 | |||||||
chr4:143595684 | A | G | 8 | a0001c0001t0001g0179 a0001c0001t0001g0190 a0001c0001t0001g0227 others(5): Show |
9 | HG01243.hp2 HG01981.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.6029-9691T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595684 | |||||||
chr4:143595694 | T | C | 5 | a0001c0001t0001g0146 a0007c0008t0001g0136 a0007c0008t0001g0238 others(2): Show |
5 | HG00741.hp1 HG01192.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6029-9701A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595694 | |||||||
chr4:143595698 | T | C | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6029-9705A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595698 | |||||||
chr4:143595744 | C | T | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6029-9751G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595744 | |||||||
chr4:143595745 | A | G | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.6029-9752T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595745 | |||||||
chr4:143595757 | A | G | 20 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
20 | HG01496.hp2 HG01981.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.6029-9764T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595757 | |||||||
chr4:143595761 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6029-9768A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595761 | |||||||
chr4:143595771 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9778G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595771 | |||||||
chr4:143595775 | T | C | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9782A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595775 | |||||||
chr4:143595777 | A | G | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6029-9784T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595777 | |||||||
chr4:143595804 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6029-9811G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595804 | |||||||
chr4:143595805 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-9812C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595805 | |||||||
chr4:143595859 | G | A | 3 | a0003c0003t0001g0107 a0021c0032t0004g0152 a0022c0031t0001g0145 |
3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6029-9866C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595859 | |||||||
chr4:143595860 | T | C | 3 | a0003c0003t0001g0107 a0021c0032t0004g0152 a0022c0031t0001g0145 |
3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6029-9867A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595860 | |||||||
chr4:143595866 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6029-9873G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595866 | |||||||
chr4:143595875 | G | A | 68 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(65): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6029-9882C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595875 | |||||||
chr4:143595889 | G | GAAAAAAA others(6): Show |
17 | a0001c0001t0001g0164 a0004c0004t0001g0090 a0004c0004t0001g0092 others(14): Show |
18 | HG01496.hp2 HG01981.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.6029-9909_6029-989 others(17): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GAAAAAAA others(7): Show |
2 | a0004c0004t0001g0096 a0007c0030t0001g0153 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6029-9910_6029-989 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GAAAAAAA others(8): Show |
1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-9911_6029-989 others(19): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GAAAAAAA others(9): Show |
3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0014c0014t0001g0052 |
4 | HG01243.hp2 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(20): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GGAAAAAA others(4): Show |
2 | a0001c0006t0001g0112 a0002c0002t0001g0027 |
2 | HG01167.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(15): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GGAAAAAA others(5): Show |
55 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0122 others(52): Show |
59 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595889 | G | GGAAAAAA others(6): Show |
11 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0171 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.6029-9897_6029-989 others(17): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595889 | |||||||
chr4:143595961 | T | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(79): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.6029-9968A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143595961 | |||||||
chr4:143596018 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6029-10025C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596018 | |||||||
chr4:143596063 | G | A | 1 | a0002c0002t0001g0051 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6029-10070C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596063 | |||||||
chr4:143596196 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.6029-10203C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596196 | |||||||
chr4:143596454 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.6029-10461G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596454 | |||||||
chr4:143596558 | T | C | 9 | a0004c0004t0001g0090 a0004c0004t0001g0093 a0004c0004t0001g0094 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.6029-10565A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596558 | |||||||
chr4:143596700 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.6029-10707G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596700 | |||||||
chr4:143596771 | TA | T | 89 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(86): Show |
93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.6029-10779delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596771 | |||||||
chr4:143596869 | T | C | 1 | a0004c0004t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6029-10876A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143596869 | |||||||
chr4:143597127 | AACAG | A | 3 | a0001c0001t0001g0155 a0001c0001t0003g0232 a0001c0001t0003g0233 |
3 | HG02559.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6029-11138_6029-11 others(10): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597127 | |||||||
chr4:143597135 | G | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0223 |
3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.6029-11142C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597135 | |||||||
chr4:143597151 | A | T | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-11158T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597151 | |||||||
chr4:143597181 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-11188G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597181 | |||||||
chr4:143597268 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6029-11275G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597268 | |||||||
chr4:143597269 | G | A | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6029-11276C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597269 | |||||||
chr4:143597370 | A | G | 1 | a0005c0005t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6029-11377T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597370 | |||||||
chr4:143597371 | T | C | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6029-11378A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597371 | |||||||
chr4:143597580 | A | G | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-11587T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597580 | |||||||
chr4:143597724 | A | T | 1 | a0007c0008t0001g0156 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6029-11731T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597724 | |||||||
chr4:143597740 | G | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6029-11747C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597740 | |||||||
chr4:143597971 | T | C | 17 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(14): Show |
17 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.6029-11978A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143597971 | |||||||
chr4:143598260 | C | A | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-12267G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598260 | |||||||
chr4:143598278 | T | C | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6029-12285A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598278 | |||||||
chr4:143598598 | GTA | G | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6029-12607_6029-12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598598 | |||||||
chr4:143598631 | G | A | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6029-12638C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143598631 | |||||||
chr4:143599424 | T | C | 15 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+11855A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599424 | |||||||
chr4:143599484 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.6028+11795T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599484 | |||||||
chr4:143599629 | A | G | 91 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(88): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.6028+11650T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599629 | |||||||
chr4:143599692 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6028+11587T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599692 | |||||||
chr4:143599695 | A | C | 15 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+11584T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599695 | |||||||
chr4:143599729 | G | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11550C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599729 | |||||||
chr4:143599766 | T | TGGGCTAG others(5): Show |
180 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.6028+11501_6028+11 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599766 | |||||||
chr4:143599803 | G | A | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11476C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599803 | |||||||
chr4:143599938 | G | T | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+11341C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599938 | |||||||
chr4:143599998 | G | A | 4 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0007c0030t0001g0153 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.6028+11281C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143599998 | |||||||
chr4:143600070 | C | T | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+11209G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600070 | |||||||
chr4:143600078 | T | C | 2 | a0001c0001t0001g0166 a0003c0003t0001g0106 |
2 | NA18968.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.6028+11201A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600078 | |||||||
chr4:143600222 | TA | T | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(70): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.6028+11056delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600222 | |||||||
chr4:143600460 | C | A | 4 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0240 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+10819G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600460 | |||||||
chr4:143600590 | T | C | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6028+10689A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600590 | |||||||
chr4:143600705 | G | A | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6028+10574C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600705 | |||||||
chr4:143600950 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6028+10329G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600950 | |||||||
chr4:143600963 | CT | C | 89 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(86): Show |
93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.6028+10315delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143600963 | |||||||
chr4:143601016 | G | A | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6028+10263C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601016 | |||||||
chr4:143601092 | T | TA | 21 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(18): Show |
21 | HG00558.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.6028+10186dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601092 | |||||||
chr4:143601135 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6028+10144G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601135 | |||||||
chr4:143601429 | C | T | 6 | a0007c0008t0001g0136 a0007c0008t0001g0156 a0007c0008t0001g0238 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+9850G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601429 | |||||||
chr4:143601474 | C | T | 91 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(88): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.6028+9805G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601474 | |||||||
chr4:143601544 | T | C | 15 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG00741.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.6028+9735A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601544 | |||||||
chr4:143601572 | C | T | 21 | a0001c0001t0001g0146 a0004c0004t0001g0078 a0004c0004t0001g0090 others(18): Show |
21 | HG00558.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.6028+9707G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601572 | |||||||
chr4:143601714 | G | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+9565C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601714 | |||||||
chr4:143601750 | G | T | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6028+9529C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143601750 | |||||||
chr4:143602017 | C | T | 90 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(87): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.6028+9262G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602017 | |||||||
chr4:143602173 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0187 |
3 | NA18979.hp1 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.6028+9106G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602173 | |||||||
chr4:143602379 | T | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.6028+8900A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602379 | |||||||
chr4:143602554 | C | T | 6 | a0007c0008t0001g0136 a0007c0008t0001g0156 a0007c0008t0001g0238 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+8725G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602554 | |||||||
chr4:143602609 | AGGAGATT others(27): Show |
A | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+8636_6028+866 others(38): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143602609 | |||||||
chr4:143603041 | T | A | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6028+8238A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603041 | |||||||
chr4:143603047 | G | A | 2 | a0001c0001t0001g0184 a0004c0004t0001g0079 |
2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.6028+8232C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603047 | |||||||
chr4:143603429 | G | A | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6028+7850C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603429 | |||||||
chr4:143603519 | C | A | 93 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(90): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.6028+7760G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603519 | |||||||
chr4:143603587 | C | T | 1 | a0003c0003t0001g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6028+7692G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603587 | |||||||
chr4:143603599 | A | G | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.6028+7680T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603599 | |||||||
chr4:143603650 | A | G | 1 | a0003c0003t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6028+7629T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603650 | |||||||
chr4:143603670 | A | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+7609T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603670 | |||||||
chr4:143603787 | C | T | 10 | a0001c0001t0001g0158 a0001c0001t0001g0196 a0001c0001t0001g0202 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.6028+7492G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143603787 | |||||||
chr4:143604211 | C | T | 6 | a0007c0008t0001g0136 a0007c0008t0001g0156 a0007c0008t0001g0238 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+7068G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604211 | |||||||
chr4:143604323 | C | T | 8 | a0001c0001t0001g0120 a0002c0002t0001g0001 a0002c0002t0001g0017 others(5): Show |
9 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.6028+6956G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604323 | |||||||
chr4:143604327 | A | G | 20 | a0004c0004t0001g0078 a0004c0004t0001g0090 a0004c0004t0001g0092 others(17): Show |
20 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.6028+6952T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604327 | |||||||
chr4:143604779 | T | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01952.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.6028+6500A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604779 | |||||||
chr4:143604833 | C | T | 2 | a0001c0001t0001g0199 a0003c0003t0001g0091 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6028+6446G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604833 | |||||||
chr4:143604986 | A | C | 4 | a0001c0001t0001g0180 a0002c0002t0001g0021 a0002c0002t0001g0027 others(1): Show |
4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.6028+6293T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143604986 | |||||||
chr4:143605046 | G | A | 82 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.6028+6233C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605046 | |||||||
chr4:143605173 | T | A | 82 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.6028+6106A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605173 | |||||||
chr4:143605297 | C | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0158 a0001c0001t0001g0196 others(28): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.6028+5982G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605297 | |||||||
chr4:143605356 | C | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6028+5923G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605356 | |||||||
chr4:143605360 | CTCCT | C | 8 | a0007c0008t0001g0136 a0007c0008t0001g0156 a0007c0008t0001g0238 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.6028+5915_6028+591 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605360 | |||||||
chr4:143605410 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.6028+5869A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605410 | |||||||
chr4:143605630 | C | T | 1 | a0005c0005t0001g0064 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6028+5649G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605630 | |||||||
chr4:143605680 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+5599G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605680 | |||||||
chr4:143605847 | G | A | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+5432C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143605847 | |||||||
chr4:143606022 | G | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+5257C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606022 | |||||||
chr4:143606077 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6028+5202G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606077 | |||||||
chr4:143606340 | T | C | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+4939A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606340 | |||||||
chr4:143606371 | C | CT | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.6028+4907dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606371 | |||||||
chr4:143606568 | T | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+4711A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606568 | |||||||
chr4:143606630 | C | T | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+4649G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606630 | |||||||
chr4:143606703 | C | A | 1 | a0003c0003t0001g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6028+4576G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606703 | |||||||
chr4:143606793 | AT | A | 96 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(93): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.6028+4485delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606793 | |||||||
chr4:143606950 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6028+4329G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143606950 | |||||||
chr4:143607219 | C | G | 5 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.6028+4060G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607219 | |||||||
chr4:143607355 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(211): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.6028+3924A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607355 | |||||||
chr4:143607475 | C | A | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+3804G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607475 | |||||||
chr4:143607830 | C | T | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+3449G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143607830 | |||||||
chr4:143608232 | A | G | 15 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.6028+3047T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608232 | |||||||
chr4:143608234 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.6028+3045C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608234 | |||||||
chr4:143608237 | A | C | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.6028+3042T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608237 | |||||||
chr4:143608325 | G | C | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6028+2954C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608325 | |||||||
chr4:143608364 | G | C | 19 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(16): Show |
20 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.6028+2915C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608364 | |||||||
chr4:143608400 | T | C | 3 | a0003c0003t0001g0107 a0021c0032t0004g0152 a0022c0031t0001g0145 |
3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6028+2879A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608400 | |||||||
chr4:143608660 | T | C | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.6028+2619A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608660 | |||||||
chr4:143608746 | T | G | 1 | a0003c0003t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6028+2533A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143608746 | |||||||
chr4:143609072 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG01952.hp1 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.6028+2207G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609072 | |||||||
chr4:143609083 | T | C | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6028+2196A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609083 | |||||||
chr4:143609096 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6028+2183T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609096 | |||||||
chr4:143609253 | G | A | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+2026C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609253 | |||||||
chr4:143609454 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.6028+1825G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609454 | |||||||
chr4:143609480 | TAA | T | 34 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0127 others(31): Show |
35 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.6028+1797_6028+179 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609480 | |||||||
chr4:143609502 | G | A | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6028+1777C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609502 | |||||||
chr4:143609688 | G | A | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+1591C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609688 | |||||||
chr4:143609694 | AT | A | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+1584delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609694 | |||||||
chr4:143609734 | T | A | 4 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6028+1545A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609734 | |||||||
chr4:143609754 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6028+1525T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609754 | |||||||
chr4:143609846 | T | C | 2 | a0001c0001t0001g0230 a0002c0002t0001g0050 |
2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6028+1433A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143609846 | |||||||
chr4:143610050 | A | T | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6028+1229T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610050 | |||||||
chr4:143610055 | A | G | 2 | a0001c0001t0001g0230 a0002c0002t0001g0050 |
2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.6028+1224T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610055 | |||||||
chr4:143610333 | G | A | 25 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(22): Show |
26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.6028+946C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610333 | |||||||
chr4:143610582 | A | G | 3 | a0003c0003t0001g0107 a0021c0032t0004g0152 a0022c0031t0001g0145 |
3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.6028+697T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610582 | |||||||
chr4:143610778 | T | C | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6028+501A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610778 | |||||||
chr4:143610838 | A | G | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.6028+441T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143610838 | |||||||
chr4:143611009 | C | T | 1 | a0004c0004t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6028+270G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611009 | |||||||
chr4:143611056 | CAAGTA | C | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.6028+218_6028+222d others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611056 | |||||||
chr4:143611111 | T | A | 25 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(22): Show |
26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.6028+168A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 6/7 | chr4 | 143611111 | |||||||
chr4:143611540 | G | A | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-13C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611540 | |||||||
chr4:143611543 | A | G | 4 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0240 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5780-16T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611543 | |||||||
chr4:143611786 | C | T | 3 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0008c0011t0001g0003 |
4 | HG02451.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5780-259G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143611786 | |||||||
chr4:143612001 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0192 |
3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.5780-474T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612001 | |||||||
chr4:143612181 | C | G | 5 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-654G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612181 | |||||||
chr4:143612221 | C | T | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.5780-694G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612221 | |||||||
chr4:143612235 | A | G | 4 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-708T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612235 | |||||||
chr4:143612334 | G | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5780-807C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612334 | |||||||
chr4:143612483 | T | G | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-956A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612483 | |||||||
chr4:143612562 | G | C | 4 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-1035C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612562 | |||||||
chr4:143612563 | T | G | 98 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.5780-1036A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612563 | |||||||
chr4:143612658 | T | G | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.5780-1131A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612658 | |||||||
chr4:143612794 | A | T | 25 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(22): Show |
26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.5780-1267T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143612794 | |||||||
chr4:143613167 | C | T | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.5780-1640G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613167 | |||||||
chr4:143613247 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5780-1720C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613247 | |||||||
chr4:143613465 | C | A | 65 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(62): Show |
68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.5780-1938G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613465 | |||||||
chr4:143613641 | T | C | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5780-2114A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613641 | |||||||
chr4:143613866 | C | G | 1 | a0003c0003t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5780-2339G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143613866 | |||||||
chr4:143614234 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5780-2707A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614234 | |||||||
chr4:143614414 | A | G | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5780-2887T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614414 | |||||||
chr4:143614502 | C | A | 4 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0007c0030t0001g0153 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-2975G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614502 | |||||||
chr4:143614522 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.5780-2995A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614522 | |||||||
chr4:143614631 | T | C | 5 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-3104A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614631 | |||||||
chr4:143614681 | C | A | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5780-3154G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614681 | |||||||
chr4:143614824 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5780-3297G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614824 | |||||||
chr4:143614851 | G | A | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-3324C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143614851 | |||||||
chr4:143615022 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5780-3495C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615022 | |||||||
chr4:143615180 | G | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-3653C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615180 | |||||||
chr4:143615191 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5780-3664C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615191 | |||||||
chr4:143615258 | C | T | 15 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5780-3731G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615258 | |||||||
chr4:143615299 | T | G | 15 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5780-3772A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615299 | |||||||
chr4:143615540 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5780-4013A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615540 | |||||||
chr4:143615679 | G | A | 5 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5780-4152C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615679 | |||||||
chr4:143615698 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5780-4171C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615698 | |||||||
chr4:143615707 | C | CA | 74 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(71): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.5780-4181dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615707 | |||||||
chr4:143615716 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5780-4189T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615716 | |||||||
chr4:143615716 | AAC | A | 4 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5780-4191_5780-419 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615716 | |||||||
chr4:143615717 | AC | A | 11 | a0004c0004t0001g0090 a0004c0004t0001g0092 a0004c0004t0001g0093 others(8): Show |
11 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.5780-4191delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615717 | |||||||
chr4:143615718 | C | A | 11 | a0002c0009t0001g0011 a0004c0004t0001g0078 a0004c0004t0001g0079 others(8): Show |
12 | HG00558.hp2 HG01168.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.5780-4191G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615718 | |||||||
chr4:143615718 | CA | C | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5780-4192delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615718 | |||||||
chr4:143615841 | G | T | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.5780-4314C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615841 | |||||||
chr4:143615844 | TC | T | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4318delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143615844 | |||||||
chr4:143616096 | A | C | 2 | a0001c0001t0001g0166 a0003c0003t0001g0106 |
2 | NA18968.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.5780-4569T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616096 | |||||||
chr4:143616142 | G | T | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4615C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616142 | |||||||
chr4:143616187 | T | C | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5780-4660A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616187 | |||||||
chr4:143616197 | G | C | 1 | a0014c0014t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5780-4670C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616197 | |||||||
chr4:143616205 | A | G | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5780-4678T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616205 | |||||||
chr4:143616278 | G | A | 1 | a0005c0022t0001g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5780-4751C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616278 | |||||||
chr4:143616446 | G | C | 1 | a0004c0004t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5779+4591C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616446 | |||||||
chr4:143616515 | A | G | 99 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(96): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.5779+4522T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616515 | |||||||
chr4:143616543 | T | C | 15 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5779+4494A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616543 | |||||||
chr4:143616547 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0192 |
3 | HG00423.hp2 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.5779+4490C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616547 | |||||||
chr4:143616561 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5779+4476G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616561 | |||||||
chr4:143616746 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5779+4291G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616746 | |||||||
chr4:143616753 | A | C | 4 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+4284T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616753 | |||||||
chr4:143616792 | C | CAAAAA | 5 | a0005c0005t0001g0063 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5779+4240_5779+424 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | |||||||
chr4:143616792 | C | CAAAAAAA others(1): Show |
18 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(15): Show |
19 | HG00558.hp2 HG01496.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.5779+4237_5779+424 others(12): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | |||||||
chr4:143616792 | C | CAAAAAAA others(3): Show |
2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5779+4235_5779+424 others(14): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616792 | |||||||
chr4:143616804 | G | A | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.5779+4233C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616804 | |||||||
chr4:143616891 | G | T | 1 | a0019c0019t0001g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5779+4146C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616891 | |||||||
chr4:143616934 | A | G | 3 | a0004c0004t0001g0097 a0004c0004t0001g0098 a0004c0004t0001g0100 |
3 | HG01496.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5779+4103T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143616934 | |||||||
chr4:143617163 | TCTTTA | T | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5779+3869_5779+387 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617163 | |||||||
chr4:143617262 | G | C | 4 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0007c0030t0001g0153 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+3775C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617262 | |||||||
chr4:143617561 | G | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5779+3476C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617561 | |||||||
chr4:143617665 | G | GGGTTTAA others(96): Show |
1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5779+3371_5779+337 others(107): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617665 | |||||||
chr4:143617665 | G | GGGTTTAA others(97): Show |
1 | a0007c0008t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5779+3371_5779+337 others(108): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617665 | |||||||
chr4:143617704 | AGAG | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5779+3330_5779+333 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617704 | |||||||
chr4:143617855 | C | T | 4 | a0001c0001t0001g0180 a0002c0002t0001g0021 a0002c0002t0001g0027 others(1): Show |
4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.5779+3182G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617855 | |||||||
chr4:143617985 | C | A | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5779+3052G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143617985 | |||||||
chr4:143618295 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5779+2742G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618295 | |||||||
chr4:143618349 | C | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5779+2688G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618349 | |||||||
chr4:143618369 | C | G | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5779+2668G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618369 | |||||||
chr4:143618504 | C | G | 1 | a0002c0002t0001g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5779+2533G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618504 | |||||||
chr4:143618621 | T | C | 99 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(96): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.5779+2416A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618621 | |||||||
chr4:143618626 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5779+2411C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618626 | |||||||
chr4:143618682 | T | C | 99 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(96): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.5779+2355A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618682 | |||||||
chr4:143618793 | G | A | 25 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(22): Show |
26 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.5779+2244C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618793 | |||||||
chr4:143618869 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5779+2168G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618869 | |||||||
chr4:143618931 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5779+2106T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143618931 | |||||||
chr4:143619089 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5779+1948G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619089 | |||||||
chr4:143619179 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5779+1858C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619179 | |||||||
chr4:143619348 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5779+1689G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619348 | |||||||
chr4:143619433 | G | A | 69 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(66): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.5779+1604C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619433 | |||||||
chr4:143619525 | C | T | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5779+1512G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619525 | |||||||
chr4:143619562 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5779+1475A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619562 | |||||||
chr4:143619563 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5779+1474G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619563 | |||||||
chr4:143619843 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5779+1194C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143619843 | |||||||
chr4:143620204 | G | A | 1 | a0003c0003t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5779+833C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620204 | |||||||
chr4:143620426 | C | T | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5779+611G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620426 | |||||||
chr4:143620434 | G | A | 30 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(27): Show |
32 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.5779+603C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620434 | |||||||
chr4:143620436 | A | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5779+601T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620436 | |||||||
chr4:143620657 | G | C | 1 | a0006c0007t0001g0249 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5779+380C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620657 | |||||||
chr4:143620895 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.5779+142C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620895 | |||||||
chr4:143620974 | C | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5779+63G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143620974 | |||||||
chr4:143621021 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5779+16G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 5/7 | chr4 | 143621021 | |||||||
chr4:143621183 | C | G | 1 | a0002c0010t0001g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5654-21G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621183 | |||||||
chr4:143621738 | G | C | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5654-576C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621738 | |||||||
chr4:143621795 | G | A | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.5654-633C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621795 | |||||||
chr4:143621923 | A | G | 66 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.5654-761T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621923 | |||||||
chr4:143621946 | G | A | 101 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(98): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.5654-784C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143621946 | |||||||
chr4:143622078 | T | C | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5654-916A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622078 | |||||||
chr4:143622091 | C | CT | 15 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0225 others(12): Show |
16 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.5654-930dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622091 | |||||||
chr4:143622203 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5654-1041G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622203 | |||||||
chr4:143622290 | C | T | 4 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0007c0030t0001g0153 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5654-1128G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622290 | |||||||
chr4:143622313 | C | T | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5654-1151G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622313 | |||||||
chr4:143622403 | C | CT | 40 | a0001c0001t0001g0007 a0001c0001t0001g0146 a0001c0001t0001g0173 others(37): Show |
41 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.5654-1242dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | |||||||
chr4:143622403 | CT | C | 10 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0160 others(7): Show |
10 | HG00558.hp2 HG01099.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.5654-1242delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | |||||||
chr4:143622403 | CTT | C | 86 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(83): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.5654-1243_5654-124 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | |||||||
chr4:143622403 | CTTT | C | 4 | a0007c0008t0001g0144 a0007c0008t0001g0147 a0007c0030t0001g0153 others(1): Show |
5 | HG02451.hp1 HG02622.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.5654-1244_5654-124 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622403 | |||||||
chr4:143622625 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0162 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5654-1463C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622625 | |||||||
chr4:143622722 | T | C | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5653+1386A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622722 | |||||||
chr4:143622797 | A | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5653+1311T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143622797 | |||||||
chr4:143623410 | A | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | HG00438.hp2 NA18962.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.5653+698T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623410 | |||||||
chr4:143623493 | T | TC | 43 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0131 others(40): Show |
43 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.5653+614dupG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | |||||||
chr4:143623493 | T | TCC | 16 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0161 others(13): Show |
17 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.5653+613_5653+614d others(4): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | |||||||
chr4:143623493 | TC | T | 68 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0123 others(65): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.5653+614delG | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | |||||||
chr4:143623493 | TCCC | T | 19 | a0004c0004t0001g0078 a0004c0004t0001g0079 a0004c0004t0001g0090 others(16): Show |
19 | HG00558.hp2 HG01261.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.5653+612_5653+614d others(5): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623493 | |||||||
chr4:143623498 | C | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0224 |
2 | HG01168.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.5653+610G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623498 | |||||||
chr4:143623554 | C | T | 1 | a0004c0004t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5653+554G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623554 | |||||||
chr4:143623573 | A | AT | 31 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(28): Show |
33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5653+534dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623573 | |||||||
chr4:143623986 | T | G | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5653+122A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 4/7 | chr4 | 143623986 | |||||||
chr4:143624574 | G | A | 100 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(97): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5423-236C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624574 | |||||||
chr4:143624601 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5423-263C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624601 | |||||||
chr4:143624844 | C | A | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5423-506G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624844 | |||||||
chr4:143624879 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5423-541C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143624879 | |||||||
chr4:143625122 | A | G | 30 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(27): Show |
31 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.5423-784T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625122 | |||||||
chr4:143625331 | C | T | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5423-993G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625331 | |||||||
chr4:143625380 | C | T | 67 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.5423-1042G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625380 | |||||||
chr4:143625551 | A | G | 31 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(28): Show |
33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5423-1213T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625551 | |||||||
chr4:143625649 | A | C | 100 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(97): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5423-1311T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625649 | |||||||
chr4:143625696 | G | T | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5423-1358C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625696 | |||||||
chr4:143625902 | CATT | C | 6 | a0007c0008t0001g0136 a0007c0008t0001g0156 a0007c0008t0001g0238 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.5423-1567_5423-156 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625902 | |||||||
chr4:143625982 | C | CA | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5422+1631dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625982 | |||||||
chr4:143625984 | C | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5422+1630G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143625984 | |||||||
chr4:143626185 | A | G | 4 | a0007c0008t0001g0156 a0008c0011t0001g0066 a0012c0018t0001g0243 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.5422+1429T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626185 | |||||||
chr4:143626204 | T | G | 2 | a0003c0003t0001g0108 a0005c0005t0001g0062 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5422+1410A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626204 | |||||||
chr4:143626434 | A | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
7 | HG00140.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.5422+1180T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626434 | |||||||
chr4:143626455 | A | G | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5422+1159T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626455 | |||||||
chr4:143626619 | C | T | 1 | a0002c0002t0001g0025 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5422+995G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626619 | |||||||
chr4:143626680 | G | C | 31 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(28): Show |
33 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.5422+934C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626680 | |||||||
chr4:143626699 | G | T | 2 | a0007c0008t0001g0136 a0007c0008t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5422+915C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626699 | |||||||
chr4:143626870 | A | C | 2 | a0005c0005t0001g0063 a0014c0014t0001g0053 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5422+744T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626870 | |||||||
chr4:143626999 | A | G | 100 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(97): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.5422+615T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143626999 | |||||||
chr4:143627170 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01069.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.5422+444C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627170 | |||||||
chr4:143627302 | T | C | 1 | a0004c0004t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5422+312A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627302 | |||||||
chr4:143627472 | G | A | 1 | a0005c0005t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5422+142C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627472 | |||||||
chr4:143627526 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5422+88G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 3/7 | chr4 | 143627526 | |||||||
chr4:143627999 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5276-239T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143627999 | |||||||
chr4:143628057 | T | C | 1 | a0002c0002t0001g0020 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5276-297A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628057 | |||||||
chr4:143628092 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5276-332C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628092 | |||||||
chr4:143628250 | T | A | 2 | a0005c0005t0001g0062 a0014c0014t0001g0053 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5276-490A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628250 | |||||||
chr4:143628301 | A | G | 4 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(1): Show |
4 | HG00558.hp2 HG02132.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-541T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628301 | |||||||
chr4:143628357 | G | A | 3 | a0003c0003t0001g0107 a0021c0032t0004g0152 a0022c0031t0001g0145 |
3 | HG02280.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5276-597C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628357 | |||||||
chr4:143628394 | C | A | 15 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.5276-634G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628394 | |||||||
chr4:143628478 | C | T | 238 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(235): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.5276-718G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628478 | |||||||
chr4:143628507 | A | G | 15 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(12): Show |
15 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.5276-747T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628507 | |||||||
chr4:143628893 | G | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-1133C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628893 | |||||||
chr4:143628984 | A | T | 4 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-1224T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143628984 | |||||||
chr4:143629029 | A | G | 239 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(236): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.5276-1269T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629029 | |||||||
chr4:143629058 | C | T | 72 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.5276-1298G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629058 | |||||||
chr4:143629418 | T | C | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5276-1658A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629418 | |||||||
chr4:143629785 | T | G | 13 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(10): Show |
13 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.5276-2025A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629785 | |||||||
chr4:143629835 | A | T | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-2075T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629835 | |||||||
chr4:143629910 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5276-2150C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629910 | |||||||
chr4:143629987 | A | G | 19 | a0001c0001t0001g0131 a0001c0001t0001g0209 a0001c0001t0001g0210 others(16): Show |
20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.5276-2227T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143629987 | |||||||
chr4:143630143 | C | T | 1 | a0011c0012t0001g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5276-2383G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630143 | |||||||
chr4:143630280 | A | G | 72 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.5276-2520T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630280 | |||||||
chr4:143630306 | C | T | 1 | a0005c0005t0001g0064 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5276-2546G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630306 | |||||||
chr4:143630451 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5276-2691T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630451 | |||||||
chr4:143630767 | T | C | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-3007A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630767 | |||||||
chr4:143630780 | A | G | 9 | a0004c0004t0001g0090 a0004c0004t0001g0092 a0004c0004t0001g0093 others(6): Show |
9 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.5276-3020T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630780 | |||||||
chr4:143630934 | C | T | 151 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(148): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.5276-3174G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143630934 | |||||||
chr4:143631292 | G | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-3532C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631292 | |||||||
chr4:143631329 | G | GTATT | 3 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0002c0002t0001g0018 |
3 | HG01099.hp1 HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.5276-3573_5276-357 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | |||||||
chr4:143631329 | G | GTATTTAT others(5): Show |
2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-3581_5276-357 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | |||||||
chr4:143631329 | GTATT | G | 18 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(15): Show |
19 | HG00558.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.5276-3573_5276-357 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631329 | |||||||
chr4:143631355 | A | G | 5 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0212 others(2): Show |
5 | HG03492.hp1 HG03688.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-3595T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631355 | |||||||
chr4:143631378 | T | C | 72 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.5276-3618A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631378 | |||||||
chr4:143631638 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-3878T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631638 | |||||||
chr4:143631694 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-3934C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143631694 | |||||||
chr4:143632033 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5276-4273G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632033 | |||||||
chr4:143632188 | G | T | 1 | a0003c0003t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5276-4428C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632188 | |||||||
chr4:143632205 | C | CA | 72 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.5276-4446dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632205 | |||||||
chr4:143632393 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-4633T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632393 | |||||||
chr4:143632634 | T | C | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-4874A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632634 | |||||||
chr4:143632810 | T | TA | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-5051dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632810 | |||||||
chr4:143632810 | TA | T | 14 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.5276-5051delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632810 | |||||||
chr4:143632854 | C | T | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-5094G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632854 | |||||||
chr4:143632954 | T | C | 1 | a0003c0003t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5276-5194A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632954 | |||||||
chr4:143632962 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-5202G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143632962 | |||||||
chr4:143633010 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5276-5250T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633010 | |||||||
chr4:143633418 | G | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-5658C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633418 | |||||||
chr4:143633544 | G | A | 14 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(11): Show |
14 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.5276-5784C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633544 | |||||||
chr4:143633668 | T | C | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-5908A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633668 | |||||||
chr4:143633798 | C | A | 1 | a0003c0003t0001g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5276-6038G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633798 | |||||||
chr4:143633825 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.5276-6065C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633825 | |||||||
chr4:143633871 | G | A | 1 | a0002c0002t0001g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5276-6111C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633871 | |||||||
chr4:143633889 | A | G | 143 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(140): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-6129T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143633889 | |||||||
chr4:143634098 | T | G | 1 | a0004c0004t0001g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5276-6338A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634098 | |||||||
chr4:143634165 | A | G | 37 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.5276-6405T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634165 | |||||||
chr4:143634326 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5276-6566T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634326 | |||||||
chr4:143634334 | T | G | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-6574A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634334 | |||||||
chr4:143634586 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5276-6826A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634586 | |||||||
chr4:143634636 | T | A | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-6876A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634636 | |||||||
chr4:143634639 | C | G | 3 | a0004c0004t0001g0097 a0004c0004t0001g0098 a0004c0004t0001g0100 |
3 | HG01496.hp2 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5276-6879G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634639 | |||||||
chr4:143634732 | A | ACT | 242 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(239): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.5276-6974_5276-697 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634732 | |||||||
chr4:143634770 | C | T | 10 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0213 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.5276-7010G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634770 | |||||||
chr4:143634850 | A | G | 2 | a0003c0003t0001g0084 a0003c0003t0001g0085 |
2 | HG00609.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.5276-7090T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143634850 | |||||||
chr4:143635682 | C | T | 1 | a0004c0004t0001g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5276-7922G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143635682 | |||||||
chr4:143636169 | T | G | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-8409A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636169 | |||||||
chr4:143636235 | A | G | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-8475T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636235 | |||||||
chr4:143636333 | C | CA | 9 | a0001c0001t0001g0119 a0001c0001t0001g0174 a0001c0001t0001g0218 others(6): Show |
10 | HG00280.hp2 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.5276-8574dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636333 | |||||||
chr4:143636333 | CA | C | 86 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(83): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.5276-8574delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636333 | |||||||
chr4:143636591 | A | G | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5276-8831T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636591 | |||||||
chr4:143636858 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5276-9098C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636858 | |||||||
chr4:143636860 | A | G | 13 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(10): Show |
13 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.5276-9100T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143636860 | |||||||
chr4:143637251 | TA | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0119 a0001c0001t0001g0124 others(59): Show |
63 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.5276-9492delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637251 | |||||||
chr4:143637547 | C | T | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-9787G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637547 | |||||||
chr4:143637732 | G | C | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5276-9972C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637732 | |||||||
chr4:143637806 | G | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0196 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.5276-10046C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637806 | |||||||
chr4:143637806 | G | T | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-10046C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143637806 | |||||||
chr4:143638069 | T | C | 143 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(140): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-10309A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638069 | |||||||
chr4:143638138 | C | T | 4 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-10378G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638138 | |||||||
chr4:143638313 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5276-10553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638313 | |||||||
chr4:143638377 | G | A | 143 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(140): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-10617C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638377 | |||||||
chr4:143638485 | A | C | 1 | a0002c0002t0001g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5276-10725T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638485 | |||||||
chr4:143638553 | C | T | 4 | a0001c0001t0001g0180 a0002c0002t0001g0021 a0002c0002t0001g0027 others(1): Show |
4 | HG01167.hp1 HG01943.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-10793G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638553 | |||||||
chr4:143638719 | C | A | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-10959G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638719 | |||||||
chr4:143638994 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0196 a0001c0001t0001g0202 others(21): Show |
25 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.5276-11234C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143638994 | |||||||
chr4:143639163 | A | C | 4 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-11403T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639163 | |||||||
chr4:143639327 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5276-11567C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639327 | |||||||
chr4:143639395 | G | C | 1 | a0003c0003t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5276-11635C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639395 | |||||||
chr4:143639407 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-11647C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639407 | |||||||
chr4:143639499 | G | A | 94 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(91): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.5276-11739C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639499 | |||||||
chr4:143639795 | T | A | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-12035A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639795 | |||||||
chr4:143639813 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5276-12053T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143639813 | |||||||
chr4:143640162 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-12402T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640162 | |||||||
chr4:143640293 | G | T | 1 | a0002c0002t0001g0025 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5276-12533C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640293 | |||||||
chr4:143640316 | A | T | 147 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(144): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.5276-12556T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640316 | |||||||
chr4:143640394 | C | T | 95 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(92): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.5276-12634G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640394 | |||||||
chr4:143640395 | A | G | 59 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(56): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.5276-12635T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640395 | |||||||
chr4:143640775 | C | T | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5276-13015G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143640775 | |||||||
chr4:143641073 | A | G | 7 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-13313T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641073 | |||||||
chr4:143641164 | T | G | 7 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-13404A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641164 | |||||||
chr4:143641320 | TAAA | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(140): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.5276-13563_5276-13 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641320 | |||||||
chr4:143641364 | A | C | 242 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(239): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.5276-13604T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641364 | |||||||
chr4:143641778 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5276-14018G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641778 | |||||||
chr4:143641972 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0160 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.5276-14212A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143641972 | |||||||
chr4:143642300 | C | T | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-14540G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642300 | |||||||
chr4:143642604 | C | A | 15 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(12): Show |
15 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5276-14844G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642604 | |||||||
chr4:143642620 | T | G | 1 | a0004c0004t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5276-14860A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642620 | |||||||
chr4:143642705 | C | A | 1 | a0002c0002t0001g0038 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5276-14945G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642705 | |||||||
chr4:143642705 | C | G | 4 | a0001c0001t0001g0199 a0003c0003t0001g0091 a0005c0005t0001g0056 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5276-14945G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143642705 | |||||||
chr4:143643024 | T | C | 2 | a0004c0004t0001g0090 a0004c0004t0001g0092 |
2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5276-15264A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643024 | |||||||
chr4:143643266 | G | A | 58 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0125 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.5276-15506C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643266 | |||||||
chr4:143643352 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5276-15592T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643352 | |||||||
chr4:143643423 | T | TA | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5276-15664_5276-15 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643423 | |||||||
chr4:143643514 | A | C | 1 | a0002c0002t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5276-15754T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643514 | |||||||
chr4:143643662 | G | A | 13 | a0003c0003t0001g0106 a0004c0004t0001g0078 a0004c0004t0001g0079 others(10): Show |
13 | HG00558.hp2 HG01496.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.5276-15902C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643662 | |||||||
chr4:143643864 | C | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-16104G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643864 | |||||||
chr4:143643865 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0225 a0001c0001t0001g0227 |
3 | HG00673.hp1 NA18963.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.5276-16105C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143643865 | |||||||
chr4:143644056 | A | G | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-16296T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644056 | |||||||
chr4:143644096 | G | A | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-16336C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644096 | |||||||
chr4:143644177 | A | ATG | 3 | a0001c0001t0001g0143 a0008c0011t0001g0066 a0014c0014t0001g0053 |
3 | HG01192.hp1 HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5276-16419_5276-16 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644177 | |||||||
chr4:143644177 | ATG | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.5276-16419_5276-16 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644177 | |||||||
chr4:143644178 | T | G | 1 | a0005c0005t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5276-16418A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644178 | |||||||
chr4:143644401 | A | G | 1 | a0020c0026t0001g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5276-16641T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644401 | |||||||
chr4:143644420 | C | T | 3 | a0003c0003t0001g0101 a0005c0005t0001g0060 a0027c0020t0001g0054 |
3 | HG01106.hp1 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5276-16660G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644420 | |||||||
chr4:143644456 | T | C | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-16696A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644456 | |||||||
chr4:143644472 | C | T | 3 | a0003c0003t0001g0101 a0005c0005t0001g0060 a0027c0020t0001g0054 |
3 | HG01106.hp1 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5276-16712G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644472 | |||||||
chr4:143644639 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-16879A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644639 | |||||||
chr4:143644766 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5276-17006G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644766 | |||||||
chr4:143644891 | A | T | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-17131T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644891 | |||||||
chr4:143644990 | G | A | 116 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-17230C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143644990 | |||||||
chr4:143645228 | T | C | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-17468A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645228 | |||||||
chr4:143645229 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5276-17469G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645229 | |||||||
chr4:143645288 | T | C | 113 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.5276-17528A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645288 | |||||||
chr4:143645358 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5276-17598C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645358 | |||||||
chr4:143645436 | C | T | 1 | a0002c0002t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5276-17676G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645436 | |||||||
chr4:143645541 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-17781A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645541 | |||||||
chr4:143645544 | C | T | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5276-17784G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645544 | |||||||
chr4:143645844 | T | G | 1 | a0002c0002t0001g0025 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5276-18084A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143645844 | |||||||
chr4:143646001 | A | G | 113 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(110): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.5276-18241T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646001 | |||||||
chr4:143646037 | G | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-18277C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646037 | |||||||
chr4:143646184 | A | G | 188 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(185): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.5276-18424T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646184 | |||||||
chr4:143646184 | A | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-18424T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646184 | |||||||
chr4:143646189 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-18429T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646189 | |||||||
chr4:143646223 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5276-18463T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646223 | |||||||
chr4:143646339 | C | T | 3 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 |
3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-18579G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646339 | |||||||
chr4:143646530 | T | C | 2 | a0007c0030t0001g0153 a0008c0011t0001g0066 |
2 | HG01192.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.5276-18770A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646530 | |||||||
chr4:143646591 | T | C | 1 | a0007c0008t0001g0156 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5276-18831A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646591 | |||||||
chr4:143646710 | G | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-18950C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646710 | |||||||
chr4:143646766 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5276-19006C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646766 | |||||||
chr4:143646772 | T | C | 6 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 others(3): Show |
7 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.5276-19012A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646772 | |||||||
chr4:143646781 | C | T | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-19021G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646781 | |||||||
chr4:143646800 | A | T | 30 | a0001c0001t0001g0174 a0001c0001t0001g0226 a0003c0003t0001g0005 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.5276-19040T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143646800 | |||||||
chr4:143647078 | G | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19318C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647078 | |||||||
chr4:143647122 | C | T | 1 | a0004c0004t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5276-19362G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647122 | |||||||
chr4:143647249 | AT | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19490delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647249 | |||||||
chr4:143647337 | T | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19577A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647337 | |||||||
chr4:143647345 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5276-19585C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647345 | |||||||
chr4:143647382 | G | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-19622C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647382 | |||||||
chr4:143647698 | T | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-19938A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647698 | |||||||
chr4:143647737 | A | G | 1 | a0006c0007t0001g0249 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5276-19977T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647737 | |||||||
chr4:143647746 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5276-19986G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647746 | |||||||
chr4:143647753 | G | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-19993C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647753 | |||||||
chr4:143647876 | A | G | 35 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5276-20116T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647876 | |||||||
chr4:143647896 | A | G | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5276-20136T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647896 | |||||||
chr4:143647921 | A | T | 189 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.5276-20161T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647921 | |||||||
chr4:143647939 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-20179G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647939 | |||||||
chr4:143647955 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-20195G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143647955 | |||||||
chr4:143648022 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5276-20262C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648022 | |||||||
chr4:143648274 | G | C | 1 | a0001c0001t0003g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5276-20514C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648274 | |||||||
chr4:143648295 | T | C | 1 | a0001c0001t0003g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5276-20535A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648295 | |||||||
chr4:143648482 | A | C | 1 | a0001c0028t0001g0110 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5276-20722T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648482 | |||||||
chr4:143648600 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5276-20840A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648600 | |||||||
chr4:143648784 | G | A | 1 | a0002c0002t0001g0031 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5276-21024C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648784 | |||||||
chr4:143648791 | C | T | 1 | a0015c0017t0001g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5276-21031G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648791 | |||||||
chr4:143648803 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5276-21043G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648803 | |||||||
chr4:143648804 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0162 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5276-21044C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648804 | |||||||
chr4:143648824 | A | G | 189 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.5276-21064T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648824 | |||||||
chr4:143648838 | A | G | 1 | a0002c0002t0001g0036 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5276-21078T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143648838 | |||||||
chr4:143649583 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5276-21823C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649583 | |||||||
chr4:143649734 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0162 |
2 | HG00140.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.5276-21974C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649734 | |||||||
chr4:143649797 | A | G | 1 | a0002c0002t0002g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5276-22037T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649797 | |||||||
chr4:143649874 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5276-22114G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649874 | |||||||
chr4:143649892 | G | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-22132C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649892 | |||||||
chr4:143649985 | G | A | 1 | a0005c0005t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5276-22225C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143649985 | |||||||
chr4:143650347 | C | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-22587G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650347 | |||||||
chr4:143650405 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0223 |
3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5276-22645T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650405 | |||||||
chr4:143650451 | T | G | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5276-22691A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650451 | |||||||
chr4:143650483 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-22723A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143650483 | |||||||
chr4:143651389 | G | A | 244 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.5276-23629C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651389 | |||||||
chr4:143651497 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.5276-23737T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651497 | |||||||
chr4:143651550 | A | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.5276-23790T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651550 | |||||||
chr4:143651714 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5276-23954A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651714 | |||||||
chr4:143651801 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5276-24041T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143651801 | |||||||
chr4:143652115 | T | TAACTC | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-24356_5276-24 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652115 | |||||||
chr4:143652134 | TCTTTTTC others(320): Show |
T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-24701_5276-24 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652134 | |||||||
chr4:143652146 | C | CT | 6 | a0001c0001t0001g0125 a0002c0002t0001g0033 a0002c0010t0001g0016 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.5276-24387dupA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | |||||||
chr4:143652146 | C | CTT | 25 | a0001c0001t0001g0174 a0001c0001t0001g0226 a0003c0003t0001g0005 others(22): Show |
26 | HG00438.hp1 HG00558.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.5276-24388_5276-24 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | |||||||
chr4:143652146 | C | CTTT | 5 | a0003c0003t0001g0084 a0003c0003t0001g0085 a0003c0003t0001g0089 others(2): Show |
5 | HG00609.hp1 HG02055.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-24389_5276-24 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | |||||||
chr4:143652146 | CT | C | 10 | a0002c0002t0001g0001 a0002c0002t0001g0020 a0003c0003t0001g0108 others(7): Show |
10 | HG01070.hp1 HG01106.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.5276-24387delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | |||||||
chr4:143652146 | CTT | C | 35 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(32): Show |
36 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.5276-24388_5276-24 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652146 | |||||||
chr4:143652215 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.5276-24455A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652215 | |||||||
chr4:143652231 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5276-24471G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652231 | |||||||
chr4:143652281 | G | A | 1 | a0003c0003t0001g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5276-24521C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652281 | |||||||
chr4:143652307 | C | T | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5276-24547G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652307 | |||||||
chr4:143652444 | G | A | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-24684C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652444 | |||||||
chr4:143652835 | G | A | 4 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 others(1): Show |
5 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-25075C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652835 | |||||||
chr4:143652986 | G | T | 189 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.5276-25226C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143652986 | |||||||
chr4:143653013 | T | G | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-25253A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653013 | |||||||
chr4:143653169 | A | G | 1 | a0005c0005t0001g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5276-25409T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653169 | |||||||
chr4:143653179 | G | A | 2 | a0002c0002t0001g0001 a0002c0002t0001g0039 |
3 | HG01074.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5276-25419C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653179 | |||||||
chr4:143653219 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-25459G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653219 | |||||||
chr4:143653229 | G | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-25469C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653229 | |||||||
chr4:143653242 | C | T | 1 | a0001c0006t0001g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5276-25482G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653242 | |||||||
chr4:143653282 | A | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-25522T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653282 | |||||||
chr4:143653288 | A | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.5276-25528T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653288 | |||||||
chr4:143653747 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5276-25987T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653747 | |||||||
chr4:143653791 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00140.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.5276-26031C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653791 | |||||||
chr4:143653947 | G | A | 189 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.5276-26187C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653947 | |||||||
chr4:143653997 | T | A | 44 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(41): Show |
47 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.5276-26237A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143653997 | |||||||
chr4:143654107 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5276-26347T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654107 | |||||||
chr4:143654304 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5276-26544A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654304 | |||||||
chr4:143654562 | C | T | 30 | a0001c0001t0001g0174 a0001c0001t0001g0226 a0003c0003t0001g0005 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.5276-26802G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654562 | |||||||
chr4:143654588 | A | G | 1 | a0005c0005t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5276-26828T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654588 | |||||||
chr4:143654656 | A | G | 1 | a0025c0023t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5276-26896T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654656 | |||||||
chr4:143654720 | G | T | 115 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.5276-26960C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654720 | |||||||
chr4:143654823 | T | TA | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5276-27064dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143654823 | |||||||
chr4:143655021 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5276-27261T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655021 | |||||||
chr4:143655151 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5276-27391A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655151 | |||||||
chr4:143655174 | C | T | 3 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 |
3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-27414G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655174 | |||||||
chr4:143655541 | T | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(121): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.5276-27781A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655541 | |||||||
chr4:143655589 | G | A | 34 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0127 others(31): Show |
35 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.5276-27829C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655589 | |||||||
chr4:143655795 | C | T | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-28035G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655795 | |||||||
chr4:143655858 | A | G | 1 | a0003c0003t0001g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5276-28098T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655858 | |||||||
chr4:143655970 | C | T | 3 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 |
3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5276-28210G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143655970 | |||||||
chr4:143656507 | A | T | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-28747T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656507 | |||||||
chr4:143656516 | C | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5276-28756G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656516 | |||||||
chr4:143656805 | A | G | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-29045T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656805 | |||||||
chr4:143656931 | A | G | 122 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5276-29171T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143656931 | |||||||
chr4:143657021 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-29261T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657021 | |||||||
chr4:143657030 | G | GA | 27 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(24): Show |
27 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.5276-29271dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657030 | |||||||
chr4:143657322 | A | G | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5276-29562T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657322 | |||||||
chr4:143657630 | T | C | 1 | a0002c0002t0001g0040 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5276-29870A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657630 | |||||||
chr4:143657779 | T | G | 195 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(192): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5276-30019A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657779 | |||||||
chr4:143657887 | T | C | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-30127A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657887 | |||||||
chr4:143657996 | C | T | 3 | a0001c0001t0001g0198 a0003c0003t0001g0108 a0005c0005t0001g0062 |
3 | HG02965.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5276-30236G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143657996 | |||||||
chr4:143658228 | G | A | 159 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(156): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.5276-30468C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658228 | |||||||
chr4:143658540 | C | A | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5276-30780G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658540 | |||||||
chr4:143658578 | T | C | 122 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5276-30818A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658578 | |||||||
chr4:143658783 | G | A | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-31023C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658783 | |||||||
chr4:143658899 | C | T | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5276-31139G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658899 | |||||||
chr4:143658948 | C | T | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-31188G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143658948 | |||||||
chr4:143659032 | CT | C | 122 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5276-31273delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659032 | |||||||
chr4:143659089 | T | TTTA | 31 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(28): Show |
32 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.5276-31332_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | |||||||
chr4:143659089 | TTTA | T | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-31332_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | |||||||
chr4:143659089 | TTTATTA | T | 3 | a0003c0003t0001g0107 a0007c0030t0001g0153 a0008c0011t0001g0066 |
3 | HG01192.hp1 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5276-31335_5276-31 others(12): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659089 | |||||||
chr4:143659090 | T | TTATTATT others(5): Show |
1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-31331_5276-31 others(18): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659090 | |||||||
chr4:143659178 | G | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0131 a0001c0001t0001g0170 others(5): Show |
8 | HG00423.hp1 HG01515.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.5276-31418C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659178 | |||||||
chr4:143659199 | C | T | 2 | a0013c0016t0001g0073 a0013c0016t0001g0074 |
2 | HG01099.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.5276-31439G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659199 | |||||||
chr4:143659357 | C | G | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-31597G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659357 | |||||||
chr4:143659394 | C | T | 1 | a0004c0004t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5276-31634G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659394 | |||||||
chr4:143659530 | C | T | 33 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(30): Show |
35 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.5276-31770G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659530 | |||||||
chr4:143659531 | G | A | 1 | a0002c0002t0001g0021 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5276-31771C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659531 | |||||||
chr4:143659562 | A | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5276-31802T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659562 | |||||||
chr4:143659578 | T | G | 194 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(191): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.5276-31818A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659578 | |||||||
chr4:143659652 | A | G | 73 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(70): Show |
77 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.5276-31892T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659652 | |||||||
chr4:143659655 | C | A | 194 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(191): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.5276-31895G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659655 | |||||||
chr4:143659687 | CA | C | 33 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(30): Show |
35 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.5276-31928delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659687 | |||||||
chr4:143659688 | A | AGTC | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-31931_5276-31 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659688 | |||||||
chr4:143659748 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5276-31988G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659748 | |||||||
chr4:143659786 | A | C | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5276-32026T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659786 | |||||||
chr4:143659837 | G | T | 1 | a0002c0002t0001g0045 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5276-32077C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659837 | |||||||
chr4:143659967 | A | C | 1 | a0005c0005t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5276-32207T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143659967 | |||||||
chr4:143660048 | T | C | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5276-32288A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660048 | |||||||
chr4:143660079 | T | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5276-32319A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660079 | |||||||
chr4:143660114 | T | C | 27 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(24): Show |
27 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.5276-32354A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660114 | |||||||
chr4:143660160 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5276-32400C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660160 | |||||||
chr4:143660164 | A | G | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5276-32404T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660164 | |||||||
chr4:143660205 | TA | T | 40 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(37): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5276-32446delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660205 | |||||||
chr4:143660224 | A | C | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5276-32464T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660224 | |||||||
chr4:143660247 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0160 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.5276-32487T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660247 | |||||||
chr4:143660247 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5276-32487T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660247 | |||||||
chr4:143660300 | A | G | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5276-32540T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660300 | |||||||
chr4:143660380 | G | C | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5276-32620C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660380 | |||||||
chr4:143660437 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0210 |
2 | NA18612.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.5275+32676T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660437 | |||||||
chr4:143660560 | G | A | 1 | a0023c0029t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5275+32553C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660560 | |||||||
chr4:143660564 | C | T | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+32549G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660564 | |||||||
chr4:143660585 | G | A | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+32528C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660585 | |||||||
chr4:143660644 | C | G | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32469G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660644 | |||||||
chr4:143660737 | T | G | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32376A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660737 | |||||||
chr4:143660800 | G | A | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+32313C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660800 | |||||||
chr4:143660807 | G | A | 40 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(37): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+32306C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660807 | |||||||
chr4:143660835 | T | G | 1 | a0003c0003t0001g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5275+32278A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660835 | |||||||
chr4:143660897 | G | A | 1 | a0002c0002t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5275+32216C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660897 | |||||||
chr4:143660910 | T | C | 3 | a0005c0005t0001g0058 a0009c0013t0001g0008 a0009c0013t0001g0246 |
4 | HG01243.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+32203A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660910 | |||||||
chr4:143660930 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.5275+32183T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660930 | |||||||
chr4:143660935 | G | T | 121 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5275+32178C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660935 | |||||||
chr4:143660985 | T | C | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+32128A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143660985 | |||||||
chr4:143661152 | G | C | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+31961C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661152 | |||||||
chr4:143661251 | A | G | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+31862T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661251 | |||||||
chr4:143661252 | C | T | 1 | a0002c0002t0001g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5275+31861G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661252 | |||||||
chr4:143661254 | T | C | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5275+31859A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661254 | |||||||
chr4:143661263 | T | A | 1 | a0023c0029t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5275+31850A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661263 | |||||||
chr4:143661286 | A | C | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+31827T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661286 | |||||||
chr4:143661359 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5275+31754C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661359 | |||||||
chr4:143661425 | C | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31688G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661425 | |||||||
chr4:143661515 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31598C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661515 | |||||||
chr4:143661573 | G | A | 1 | a0007c0008t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5275+31540C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661573 | |||||||
chr4:143661601 | T | C | 248 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(245): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.5275+31512A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661601 | |||||||
chr4:143661712 | C | T | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+31401G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661712 | |||||||
chr4:143661746 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31367C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661746 | |||||||
chr4:143661832 | G | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31281C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661832 | |||||||
chr4:143661926 | A | G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31187T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661926 | |||||||
chr4:143661963 | A | G | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+31150T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143661963 | |||||||
chr4:143662050 | T | C | 8 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(5): Show |
9 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.5275+31063A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662050 | |||||||
chr4:143662068 | G | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+31045C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662068 | |||||||
chr4:143662128 | C | A | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30985G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662128 | |||||||
chr4:143662168 | T | C | 3 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 |
3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5275+30945A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662168 | |||||||
chr4:143662202 | T | C | 1 | a0008c0011t0001g0003 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+30911A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662202 | |||||||
chr4:143662252 | T | A | 3 | a0005c0005t0001g0056 a0005c0005t0001g0059 a0005c0022t0001g0065 |
3 | HG02630.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5275+30861A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662252 | |||||||
chr4:143662258 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30855C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662258 | |||||||
chr4:143662279 | G | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30834C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662279 | |||||||
chr4:143662314 | A | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30799T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662314 | |||||||
chr4:143662407 | T | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0170 others(1): Show |
4 | HG01099.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+30706A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662407 | |||||||
chr4:143662529 | A | AGGTGT | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30579_5275+30 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662529 | |||||||
chr4:143662549 | T | G | 1 | a0020c0026t0001g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+30564A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662549 | |||||||
chr4:143662617 | A | T | 40 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(37): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+30496T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662617 | |||||||
chr4:143662942 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30171G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143662942 | |||||||
chr4:143663007 | A | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+30106T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663007 | |||||||
chr4:143663021 | T | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30092A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663021 | |||||||
chr4:143663046 | C | G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+30067G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663046 | |||||||
chr4:143663052 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5275+30061C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663052 | |||||||
chr4:143663082 | C | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5275+30031G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663082 | |||||||
chr4:143663106 | C | G | 33 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0134 others(30): Show |
35 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.5275+30007G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663106 | |||||||
chr4:143663123 | A | G | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+29990T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663123 | |||||||
chr4:143663151 | G | C | 1 | a0014c0014t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+29962C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663151 | |||||||
chr4:143663244 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5275+29869C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663244 | |||||||
chr4:143663276 | C | T | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+29837G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663276 | |||||||
chr4:143663294 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5275+29819G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663294 | |||||||
chr4:143663403 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5275+29710T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663403 | |||||||
chr4:143663418 | C | G | 1 | a0003c0003t0001g0083 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5275+29695G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663418 | |||||||
chr4:143663452 | T | C | 194 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(191): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.5275+29661A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663452 | |||||||
chr4:143663568 | G | A | 48 | a0001c0001t0001g0125 a0001c0001t0001g0138 a0001c0001t0001g0182 others(45): Show |
51 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.5275+29545C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663568 | |||||||
chr4:143663584 | C | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+29529G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663584 | |||||||
chr4:143663598 | A | G | 1 | a0002c0002t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5275+29515T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663598 | |||||||
chr4:143663701 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5275+29412T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663701 | |||||||
chr4:143663807 | C | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG00099.hp2 HG00323.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.5275+29306G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663807 | |||||||
chr4:143663817 | C | T | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+29296G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663817 | |||||||
chr4:143663818 | G | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+29295C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663818 | |||||||
chr4:143663870 | A | G | 3 | a0007c0008t0001g0136 a0012c0018t0001g0243 a0012c0018t0001g0244 |
3 | HG01070.hp2 HG01071.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5275+29243T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663870 | |||||||
chr4:143663872 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+29241G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663872 | |||||||
chr4:143663914 | G | A | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+29199C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143663914 | |||||||
chr4:143664061 | G | A | 2 | a0007c0008t0001g0144 a0007c0008t0001g0147 |
2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5275+29052C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664061 | |||||||
chr4:143664080 | C | T | 3 | a0003c0003t0001g0080 a0003c0003t0001g0081 a0003c0003t0001g0082 |
3 | NA18957.hp2 NA19079.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.5275+29033G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664080 | |||||||
chr4:143664146 | A | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+28967T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664146 | |||||||
chr4:143664283 | T | C | 19 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0131 others(16): Show |
19 | HG00423.hp1 HG00741.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.5275+28830A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664283 | |||||||
chr4:143664293 | T | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+28820A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664293 | |||||||
chr4:143664305 | A | T | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5275+28808T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664305 | |||||||
chr4:143664451 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0223 |
3 | HG03492.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5275+28662C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664451 | |||||||
chr4:143664567 | C | T | 40 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(37): Show |
42 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.5275+28546G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664567 | |||||||
chr4:143664575 | G | C | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+28538C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664575 | |||||||
chr4:143664701 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.5275+28412G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664701 | |||||||
chr4:143664705 | G | A | 1 | a0005c0005t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5275+28408C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664705 | |||||||
chr4:143664780 | G | A | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+28333C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664780 | |||||||
chr4:143664810 | A | G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+28303T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664810 | |||||||
chr4:143664894 | G | T | 126 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.5275+28219C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664894 | |||||||
chr4:143664895 | G | T | 4 | a0006c0007t0001g0009 a0006c0007t0001g0249 a0006c0007t0001g0250 others(1): Show |
5 | HG02132.hp2 NA18943.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.5275+28218C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664895 | |||||||
chr4:143664934 | C | T | 1 | a0014c0014t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+28179G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143664934 | |||||||
chr4:143665009 | G | A | 1 | a0001c0028t0001g0110 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5275+28104C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665009 | |||||||
chr4:143665129 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5275+27984T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665129 | |||||||
chr4:143665136 | T | C | 196 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(193): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.5275+27977A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665136 | |||||||
chr4:143665169 | C | T | 1 | a0004c0004t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5275+27944G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665169 | |||||||
chr4:143665188 | G | A | 3 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 |
3 | HG01433.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5275+27925C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665188 | |||||||
chr4:143665211 | G | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+27902C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665211 | |||||||
chr4:143665264 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+27849G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665264 | |||||||
chr4:143665264 | C | T | 122 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5275+27849G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665264 | |||||||
chr4:143665358 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5275+27755A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665358 | |||||||
chr4:143665467 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+27646C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665467 | |||||||
chr4:143665524 | T | A | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.5275+27589A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665524 | |||||||
chr4:143665526 | C | A | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.5275+27587G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665526 | |||||||
chr4:143665526 | C | T | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+27587G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665526 | |||||||
chr4:143665748 | G | C | 196 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(193): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.5275+27365C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665748 | |||||||
chr4:143665903 | T | C | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+27210A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143665903 | |||||||
chr4:143666078 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+27035G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666078 | |||||||
chr4:143666203 | A | G | 6 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(3): Show |
6 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+26910T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666203 | |||||||
chr4:143666217 | C | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+26896G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666217 | |||||||
chr4:143666536 | G | A | 7 | a0003c0003t0001g0107 a0005c0005t0001g0056 a0005c0005t0001g0059 others(4): Show |
8 | HG01192.hp1 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.5275+26577C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666536 | |||||||
chr4:143666555 | A | G | 1 | a0003c0003t0001g0107 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5275+26558T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666555 | |||||||
chr4:143666698 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+26415A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666698 | |||||||
chr4:143666841 | G | A | 123 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.5275+26272C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666841 | |||||||
chr4:143666962 | G | T | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+26151C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143666962 | |||||||
chr4:143667053 | T | C | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+26060A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667053 | |||||||
chr4:143667441 | T | A | 1 | a0005c0005t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5275+25672A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667441 | |||||||
chr4:143667484 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+25629G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667484 | |||||||
chr4:143667657 | A | C | 29 | a0001c0001t0001g0174 a0003c0003t0001g0005 a0003c0003t0001g0075 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+25456T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667657 | |||||||
chr4:143667908 | A | G | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+25205T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143667908 | |||||||
chr4:143668892 | G | A | 32 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(29): Show |
33 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.5275+24221C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668892 | |||||||
chr4:143668927 | A | G | 243 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(240): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.5275+24186T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668927 | |||||||
chr4:143668972 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+24141G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143668972 | |||||||
chr4:143669056 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0133 |
2 | HG01099.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.5275+24057C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669056 | |||||||
chr4:143669217 | C | T | 1 | a0003c0003t0001g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5275+23896G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669217 | |||||||
chr4:143669332 | G | T | 18 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(15): Show |
18 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.5275+23781C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669332 | |||||||
chr4:143669422 | G | A | 1 | a0003c0003t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5275+23691C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669422 | |||||||
chr4:143669433 | C | T | 3 | a0002c0010t0001g0014 a0002c0010t0001g0015 a0002c0010t0001g0016 |
3 | HG02559.hp1 HG03710.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.5275+23680G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669433 | |||||||
chr4:143669656 | G | GA | 10 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0237 others(7): Show |
11 | HG01069.hp1 HG01106.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.5275+23456dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669656 | |||||||
chr4:143669927 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+23186G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669927 | |||||||
chr4:143669928 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5275+23185G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143669928 | |||||||
chr4:143670062 | C | T | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+23051G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670062 | |||||||
chr4:143670074 | C | A | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+23039G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670074 | |||||||
chr4:143670115 | C | CA | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+22997dupT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670115 | |||||||
chr4:143670354 | C | T | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+22759G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670354 | |||||||
chr4:143670901 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5275+22212C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143670901 | |||||||
chr4:143671120 | C | T | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+21993G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671120 | |||||||
chr4:143671301 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5275+21812G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671301 | |||||||
chr4:143671320 | C | T | 1 | a0005c0005t0001g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5275+21793G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671320 | |||||||
chr4:143671586 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5275+21527A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671586 | |||||||
chr4:143671901 | A | G | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5275+21212T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671901 | |||||||
chr4:143671992 | C | T | 1 | a0007c0008t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5275+21121G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143671992 | |||||||
chr4:143672009 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+21104T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672009 | |||||||
chr4:143672069 | C | T | 1 | a0018c0035t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5275+21044G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672069 | |||||||
chr4:143672137 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5275+20976T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672137 | |||||||
chr4:143672300 | T | C | 1 | a0003c0003t0001g0095 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5275+20813A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672300 | |||||||
chr4:143672549 | T | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01257.hp1 HG01496.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.5275+20564A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672549 | |||||||
chr4:143672680 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+20433T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672680 | |||||||
chr4:143672740 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+20373T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672740 | |||||||
chr4:143672835 | G | A | 2 | a0003c0003t0001g0106 a0004c0004t0001g0105 |
2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.5275+20278C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672835 | |||||||
chr4:143672995 | T | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+20118A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143672995 | |||||||
chr4:143673034 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5275+20079G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673034 | |||||||
chr4:143673068 | G | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+20045C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673068 | |||||||
chr4:143673138 | G | A | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+19975C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673138 | |||||||
chr4:143673158 | G | A | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
39 | HG00438.hp1 HG00609.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.5275+19955C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673158 | |||||||
chr4:143673270 | G | A | 10 | a0005c0005t0001g0056 a0005c0005t0001g0057 a0005c0005t0001g0058 others(7): Show |
10 | HG01106.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5275+19843C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673270 | |||||||
chr4:143673370 | T | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19743A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673370 | |||||||
chr4:143673384 | C | T | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+19729G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673384 | |||||||
chr4:143673428 | T | C | 2 | a0001c0001t0003g0232 a0001c0001t0003g0233 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5275+19685A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673428 | |||||||
chr4:143673475 | G | A | 1 | a0007c0030t0001g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5275+19638C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673475 | |||||||
chr4:143673499 | C | T | 1 | a0003c0003t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5275+19614G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673499 | |||||||
chr4:143673568 | G | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19545C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673568 | |||||||
chr4:143673664 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5275+19449G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673664 | |||||||
chr4:143673673 | A | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+19440T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673673 | |||||||
chr4:143673710 | C | G | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+19403G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673710 | |||||||
chr4:143673760 | G | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+19353C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673760 | |||||||
chr4:143673871 | G | C | 1 | a0002c0002t0001g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5275+19242C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673871 | |||||||
chr4:143673881 | C | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+19232G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143673881 | |||||||
chr4:143674022 | C | T | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+19091G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674022 | |||||||
chr4:143674049 | C | T | 13 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.5275+19064G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674049 | |||||||
chr4:143674074 | C | T | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+19039G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674074 | |||||||
chr4:143674138 | G | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+18975C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674138 | |||||||
chr4:143674154 | ATGCAGAA others(13): Show |
A | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+18939_5275+18 others(26): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674154 | |||||||
chr4:143674169 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18944T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674169 | |||||||
chr4:143674213 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+18900G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674213 | |||||||
chr4:143674284 | C | A | 1 | a0002c0002t0001g0045 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5275+18829G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674284 | |||||||
chr4:143674355 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18758T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674355 | |||||||
chr4:143674375 | A | G | 4 | a0001c0001t0001g0203 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG00673.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+18738T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674375 | |||||||
chr4:143674415 | C | T | 36 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(33): Show |
37 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.5275+18698G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674415 | |||||||
chr4:143674510 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02257.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5275+18603G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674510 | |||||||
chr4:143674653 | T | C | 236 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5275+18460A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674653 | |||||||
chr4:143674707 | C | A | 120 | a0001c0001t0001g0007 a0001c0001t0001g0118 a0001c0001t0001g0119 others(117): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.5275+18406G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674707 | |||||||
chr4:143674770 | C | A | 35 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+18343G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674770 | |||||||
chr4:143674789 | A | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18324T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674789 | |||||||
chr4:143674801 | C | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+18312G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674801 | |||||||
chr4:143674859 | T | A | 3 | a0003c0003t0001g0107 a0003c0003t0001g0108 a0024c0021t0001g0055 |
3 | HG03041.hp2 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5275+18254A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674859 | |||||||
chr4:143674886 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0208 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.5275+18227T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143674886 | |||||||
chr4:143675248 | G | A | 1 | a0005c0005t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5275+17865C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675248 | |||||||
chr4:143675304 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5275+17809C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675304 | |||||||
chr4:143675306 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5275+17807T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675306 | |||||||
chr4:143675312 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17801T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675312 | |||||||
chr4:143675321 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17792T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675321 | |||||||
chr4:143675343 | G | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17770C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675343 | |||||||
chr4:143675354 | C | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+17759G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675354 | |||||||
chr4:143675384 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5275+17729A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675384 | |||||||
chr4:143675533 | C | T | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+17580G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675533 | |||||||
chr4:143675593 | G | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17520C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675593 | |||||||
chr4:143675647 | G | A | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+17466C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675647 | |||||||
chr4:143675704 | G | A | 2 | a0005c0005t0001g0061 a0005c0005t0001g0062 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5275+17409C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675704 | |||||||
chr4:143675707 | A | C | 1 | a0002c0002t0001g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5275+17406T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675707 | |||||||
chr4:143675788 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17325A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675788 | |||||||
chr4:143675811 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17302G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675811 | |||||||
chr4:143675816 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+17297C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675816 | |||||||
chr4:143675861 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5275+17252A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675861 | |||||||
chr4:143675866 | C | A | 2 | a0003c0003t0001g0107 a0003c0003t0001g0108 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+17247G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675866 | |||||||
chr4:143675876 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5275+17237G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675876 | |||||||
chr4:143675884 | C | T | 236 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5275+17229G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143675884 | |||||||
chr4:143676018 | T | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+17095A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676018 | |||||||
chr4:143676070 | C | T | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+17043G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676070 | |||||||
chr4:143676126 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG02257.hp2 HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5275+16987C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676126 | |||||||
chr4:143676159 | T | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+16954A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676159 | |||||||
chr4:143676200 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+16913T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676200 | |||||||
chr4:143676255 | T | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5275+16858A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676255 | |||||||
chr4:143676323 | C | T | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+16790G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676323 | |||||||
chr4:143676331 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16782T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676331 | |||||||
chr4:143676343 | C | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01257.hp1 HG01496.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.5275+16770G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676343 | |||||||
chr4:143676386 | G | T | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+16727C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676386 | |||||||
chr4:143676421 | T | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16692A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676421 | |||||||
chr4:143676499 | T | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16614A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676499 | |||||||
chr4:143676560 | T | C | 39 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(36): Show |
41 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.5275+16553A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676560 | |||||||
chr4:143676784 | T | C | 2 | a0003c0003t0001g0107 a0003c0003t0001g0108 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+16329A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676784 | |||||||
chr4:143676809 | A | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16304T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676809 | |||||||
chr4:143676819 | A | G | 239 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.5275+16294T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676819 | |||||||
chr4:143676844 | A | C | 235 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(232): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.5275+16269T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676844 | |||||||
chr4:143676868 | AACC | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+16242_5275+16 others(9): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676868 | |||||||
chr4:143676923 | G | C | 1 | a0020c0026t0001g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16190C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676923 | |||||||
chr4:143676929 | A | G | 1 | a0020c0026t0001g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16184T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676929 | |||||||
chr4:143676930 | A | G | 1 | a0020c0026t0001g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5275+16183T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676930 | |||||||
chr4:143676999 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+16114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143676999 | |||||||
chr4:143677213 | G | T | 17 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0120 others(14): Show |
17 | HG00099.hp2 HG00323.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.5275+15900C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677213 | |||||||
chr4:143677411 | T | G | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15702A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677411 | |||||||
chr4:143677461 | A | C | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+15652T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677461 | |||||||
chr4:143677571 | G | C | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15542C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677571 | |||||||
chr4:143677590 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5275+15523C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677590 | |||||||
chr4:143677617 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+15496A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677617 | |||||||
chr4:143677627 | A | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+15486T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677627 | |||||||
chr4:143677652 | A | G | 13 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG00423.hp1 HG00609.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.5275+15461T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677652 | |||||||
chr4:143677700 | A | T | 1 | a0015c0017t0001g0207 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5275+15413T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677700 | |||||||
chr4:143677740 | G | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+15373C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677740 | |||||||
chr4:143677901 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+15212T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677901 | |||||||
chr4:143677922 | A | G | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+15191T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677922 | |||||||
chr4:143677942 | G | A | 1 | a0007c0008t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5275+15171C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143677942 | |||||||
chr4:143678128 | T | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14985A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678128 | |||||||
chr4:143678233 | C | G | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+14880G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678233 | |||||||
chr4:143678308 | G | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14805C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678308 | |||||||
chr4:143678443 | T | G | 1 | a0015c0017t0001g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5275+14670A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678443 | |||||||
chr4:143678543 | A | AAT | 5 | a0005c0005t0001g0056 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+14568_5275+14 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678543 | |||||||
chr4:143678545 | T | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14568A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678545 | |||||||
chr4:143678575 | C | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+14538G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678575 | |||||||
chr4:143678761 | T | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14352A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678761 | |||||||
chr4:143678851 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+14262T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678851 | |||||||
chr4:143678882 | A | ATATGT | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+14230_5275+14 others(11): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143678882 | |||||||
chr4:143679071 | C | T | 1 | a0006c0007t0001g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5275+14042G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679071 | |||||||
chr4:143679158 | C | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+13955G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679158 | |||||||
chr4:143679161 | A | C | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+13952T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679161 | |||||||
chr4:143679244 | A | G | 5 | a0004c0004t0001g0096 a0004c0004t0001g0097 a0004c0004t0001g0098 others(2): Show |
5 | HG01496.hp2 HG02055.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5275+13869T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679244 | |||||||
chr4:143679246 | G | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG00438.hp2 NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.5275+13867C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679246 | |||||||
chr4:143679313 | G | A | 13 | a0005c0005t0001g0056 a0005c0005t0001g0057 a0005c0005t0001g0058 others(10): Show |
14 | HG01106.hp1 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5275+13800C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679313 | |||||||
chr4:143679425 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5275+13688C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679425 | |||||||
chr4:143679476 | A | G | 2 | a0003c0003t0001g0107 a0003c0003t0001g0108 |
2 | HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5275+13637T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679476 | |||||||
chr4:143679506 | T | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0155 others(3): Show |
6 | HG01261.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+13607A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679506 | |||||||
chr4:143679525 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+13588G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679525 | |||||||
chr4:143679715 | A | T | 35 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+13398T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679715 | |||||||
chr4:143679999 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+13114T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143679999 | |||||||
chr4:143680038 | T | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+13075A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680038 | |||||||
chr4:143680118 | A | G | 43 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(40): Show |
46 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.5275+12995T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680118 | |||||||
chr4:143680140 | T | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+12973A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680140 | |||||||
chr4:143680150 | T | G | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12963A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680150 | |||||||
chr4:143680216 | CTA | C | 35 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+12895_5275+12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680216 | |||||||
chr4:143680250 | A | G | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12863T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680250 | |||||||
chr4:143680256 | C | CAT | 41 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(38): Show |
43 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.5275+12855_5275+12 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680256 | |||||||
chr4:143680323 | T | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0194 |
2 | NA18953.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.5275+12790A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680323 | |||||||
chr4:143680430 | A | G | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12683T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680430 | |||||||
chr4:143680484 | G | C | 3 | a0003c0003t0001g0107 a0003c0003t0001g0108 a0024c0021t0001g0055 |
3 | HG03041.hp2 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5275+12629C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680484 | |||||||
chr4:143680625 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5275+12488T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680625 | |||||||
chr4:143680677 | C | A | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+12436G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680677 | |||||||
chr4:143680691 | G | T | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12422C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680691 | |||||||
chr4:143680693 | G | A | 53 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(50): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.5275+12420C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680693 | |||||||
chr4:143680732 | T | C | 48 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.5275+12381A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680732 | |||||||
chr4:143680788 | T | C | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+12325A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680788 | |||||||
chr4:143680836 | A | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+12277T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143680836 | |||||||
chr4:143681293 | T | C | 1 | a0002c0002t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5275+11820A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681293 | |||||||
chr4:143681847 | A | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+11266T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681847 | |||||||
chr4:143681975 | G | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+11138C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143681975 | |||||||
chr4:143682050 | C | A | 43 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(40): Show |
46 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.5275+11063G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682050 | |||||||
chr4:143682151 | A | G | 1 | a0004c0004t0001g0090 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5275+10962T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682151 | |||||||
chr4:143682167 | A | C | 1 | a0002c0002t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5275+10946T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682167 | |||||||
chr4:143682342 | A | G | 6 | a0003c0003t0001g0091 a0003c0003t0001g0095 a0004c0004t0001g0090 others(3): Show |
6 | HG02486.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+10771T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682342 | |||||||
chr4:143682402 | G | A | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+10711C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682402 | |||||||
chr4:143682426 | C | T | 18 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(15): Show |
19 | HG00280.hp1 HG01167.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.5275+10687G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682426 | |||||||
chr4:143682541 | T | C | 48 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.5275+10572A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682541 | |||||||
chr4:143682602 | G | A | 1 | a0014c0014t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5275+10511C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682602 | |||||||
chr4:143682614 | A | G | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+10499T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682614 | |||||||
chr4:143682744 | A | G | 1 | a0014c0014t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5275+10369T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682744 | |||||||
chr4:143682753 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5275+10360C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682753 | |||||||
chr4:143682990 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+10123T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143682990 | |||||||
chr4:143683066 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5275+10047G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683066 | |||||||
chr4:143683131 | T | C | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+9982A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683131 | |||||||
chr4:143683229 | T | C | 4 | a0001c0001t0001g0203 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG00673.hp1 NA18963.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+9884A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683229 | |||||||
chr4:143683335 | C | A | 5 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+9778G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683335 | |||||||
chr4:143683450 | A | G | 2 | a0002c0002t0001g0020 a0002c0002t0001g0025 |
2 | HG00639.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.5275+9663T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683450 | |||||||
chr4:143683855 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+9258G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683855 | |||||||
chr4:143683884 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+9229G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683884 | |||||||
chr4:143683985 | A | G | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+9128T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143683985 | |||||||
chr4:143684069 | C | A | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5275+9044G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684069 | |||||||
chr4:143684392 | T | C | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8721A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684392 | |||||||
chr4:143684509 | C | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+8604G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684509 | |||||||
chr4:143684721 | C | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8392G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684721 | |||||||
chr4:143684948 | A | AACAAAG | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+8164_5275+816 others(10): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684948 | |||||||
chr4:143684950 | G | C | 236 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(233): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.5275+8163C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143684950 | |||||||
chr4:143685113 | G | A | 2 | a0008c0011t0001g0003 a0025c0023t0001g0067 |
3 | HG03453.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5275+8000C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685113 | |||||||
chr4:143685211 | C | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+7902G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685211 | |||||||
chr4:143685371 | G | T | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+7742C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685371 | |||||||
chr4:143685478 | T | G | 35 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+7635A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685478 | |||||||
chr4:143685727 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5275+7386T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685727 | |||||||
chr4:143685862 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+7251T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685862 | |||||||
chr4:143685957 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5275+7156G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143685957 | |||||||
chr4:143686508 | C | T | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+6605G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686508 | |||||||
chr4:143686789 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+6324T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686789 | |||||||
chr4:143686811 | G | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+6302C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686811 | |||||||
chr4:143686927 | C | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+6186G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686927 | |||||||
chr4:143686997 | C | T | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+6116G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143686997 | |||||||
chr4:143687190 | C | T | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+5923G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687190 | |||||||
chr4:143687209 | G | A | 3 | a0008c0011t0001g0003 a0008c0011t0001g0066 a0025c0023t0001g0067 |
4 | HG01192.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+5904C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687209 | |||||||
chr4:143687213 | C | T | 42 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(39): Show |
44 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.5275+5900G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687213 | |||||||
chr4:143687214 | G | A | 24 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(21): Show |
25 | HG00140.hp1 HG00738.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.5275+5899C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687214 | |||||||
chr4:143687229 | C | T | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+5884G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687229 | |||||||
chr4:143687283 | C | T | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+5830G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687283 | |||||||
chr4:143687314 | G | T | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+5799C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687314 | |||||||
chr4:143687348 | G | GTAA | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+5764_5275+576 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687348 | |||||||
chr4:143687860 | C | T | 1 | a0002c0010t0001g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5275+5253G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687860 | |||||||
chr4:143687886 | ACAAACCC others(5): Show |
A | 1 | a0002c0010t0001g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5275+5215_5275+522 others(16): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687886 | |||||||
chr4:143687990 | A | C | 1 | a0002c0002t0001g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5275+5123T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143687990 | |||||||
chr4:143688029 | G | A | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+5084C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688029 | |||||||
chr4:143688180 | G | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5275+4933C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688180 | |||||||
chr4:143688197 | G | A | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+4916C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688197 | |||||||
chr4:143688357 | A | G | 38 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.5275+4756T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688357 | |||||||
chr4:143688715 | G | A | 61 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(58): Show |
65 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.5275+4398C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688715 | |||||||
chr4:143688917 | A | G | 1 | a0007c0008t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5275+4196T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688917 | |||||||
chr4:143688946 | C | G | 35 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5275+4167G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688946 | |||||||
chr4:143688997 | A | G | 1 | a0002c0002t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5275+4116T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143688997 | |||||||
chr4:143689187 | A | C | 1 | a0008c0011t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5275+3926T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689187 | |||||||
chr4:143689372 | A | T | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+3741T>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689372 | |||||||
chr4:143689583 | C | T | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+3530G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689583 | |||||||
chr4:143689669 | G | GAT | 5 | a0002c0002t0001g0023 a0011c0012t0001g0004 a0011c0012t0001g0068 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.5275+3442_5275+344 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143689669 | |||||||
chr4:143690017 | TA | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.5275+3095delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | |||||||
chr4:143690017 | TAA | T | 21 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(18): Show |
21 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.5275+3094_5275+309 others(6): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | |||||||
chr4:143690017 | TAAA | T | 37 | a0001c0001t0001g0122 a0001c0001t0001g0205 a0003c0003t0001g0005 others(34): Show |
38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.5275+3093_5275+309 others(7): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | |||||||
chr4:143690017 | TAAAA | T | 6 | a0003c0003t0001g0075 a0009c0013t0001g0008 a0009c0013t0001g0246 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.5275+3092_5275+309 others(8): Show |
FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690017 | |||||||
chr4:143690104 | G | A | 239 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.5275+3009C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690104 | |||||||
chr4:143690106 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5275+3007A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690106 | |||||||
chr4:143690420 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5275+2693G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690420 | |||||||
chr4:143690436 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5275+2677G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690436 | |||||||
chr4:143690470 | G | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+2643C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690470 | |||||||
chr4:143690753 | A | G | 1 | a0011c0012t0001g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5275+2360T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690753 | |||||||
chr4:143690784 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5275+2329T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690784 | |||||||
chr4:143690903 | C | T | 3 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 |
3 | HG01433.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5275+2210G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690903 | |||||||
chr4:143690951 | T | C | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+2162A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690951 | |||||||
chr4:143690953 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5275+2160C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143690953 | |||||||
chr4:143691099 | G | A | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5275+2014C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691099 | |||||||
chr4:143691127 | G | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5275+1986C>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691127 | |||||||
chr4:143691172 | C | G | 1 | a0018c0035t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5275+1941G>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691172 | |||||||
chr4:143691323 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(135): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.5275+1790C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691323 | |||||||
chr4:143691384 | C | T | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1729G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691384 | |||||||
chr4:143691418 | TA | T | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1694delT | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691418 | |||||||
chr4:143691501 | G | A | 30 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0173 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.5275+1612C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691501 | |||||||
chr4:143691504 | A | G | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+1609T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691504 | |||||||
chr4:143691519 | G | A | 64 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(61): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.5275+1594C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691519 | |||||||
chr4:143691585 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5275+1528T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691585 | |||||||
chr4:143691717 | G | A | 1 | a0003c0003t0001g0005 | 2 | NA18969.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.5275+1396C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691717 | |||||||
chr4:143691747 | T | A | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1366A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691747 | |||||||
chr4:143691776 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5275+1337T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691776 | |||||||
chr4:143691825 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5275+1288C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691825 | |||||||
chr4:143691870 | AT | A | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5275+1242delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691870 | |||||||
chr4:143691920 | T | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+1193A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691920 | |||||||
chr4:143691943 | T | A | 5 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0012c0018t0001g0243 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.5275+1170A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691943 | |||||||
chr4:143691952 | T | G | 2 | a0009c0013t0001g0008 a0009c0013t0001g0246 |
3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5275+1161A>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143691952 | |||||||
chr4:143692103 | T | A | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5275+1010A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692103 | |||||||
chr4:143692663 | C | T | 247 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0117 others(244): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.5275+450G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692663 | |||||||
chr4:143692709 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+404C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692709 | |||||||
chr4:143692752 | T | A | 3 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0018c0035t0001g0245 |
4 | HG01243.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5275+361A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692752 | |||||||
chr4:143692897 | G | T | 1 | a0017c0025t0001g0070 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5275+216C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143692897 | |||||||
chr4:143693019 | C | A | 4 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0014c0014t0001g0052 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5275+94G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 2/7 | chr4 | 143693019 | |||||||
chr4:143693290 | G | T | 13 | a0005c0005t0001g0056 a0005c0005t0001g0057 a0005c0005t0001g0058 others(10): Show |
14 | HG01106.hp1 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5186-88C>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693290 | |||||||
chr4:143693377 | T | A | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5186-175A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693377 | |||||||
chr4:143693430 | T | A | 5 | a0009c0013t0001g0008 a0009c0013t0001g0246 a0012c0018t0001g0243 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.5186-228A>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693430 | |||||||
chr4:143693496 | G | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0202 a0001c0001t0001g0203 others(29): Show |
33 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.5186-294C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693496 | |||||||
chr4:143693518 | A | G | 69 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(66): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.5186-316T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693518 | |||||||
chr4:143693954 | C | A | 3 | a0011c0012t0001g0004 a0011c0012t0001g0068 a0016c0024t0001g0069 |
4 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.5186-752G>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693954 | |||||||
chr4:143693955 | A | C | 1 | a0024c0021t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5186-753T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143693955 | |||||||
chr4:143694268 | T | C | 37 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(34): Show |
38 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.5186-1066A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694268 | |||||||
chr4:143694302 | G | A | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5186-1100C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694302 | |||||||
chr4:143694363 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5185+1128T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694363 | |||||||
chr4:143694369 | G | A | 3 | a0001c0001t0003g0232 a0001c0001t0003g0233 a0023c0029t0001g0231 |
3 | HG02559.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5185+1122C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694369 | |||||||
chr4:143694452 | AT | A | 14 | a0001c0001t0001g0234 a0005c0005t0001g0056 a0005c0005t0001g0057 others(11): Show |
15 | HG01106.hp1 HG01192.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.5185+1038delA | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694452 | |||||||
chr4:143694565 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.5185+926C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694565 | |||||||
chr4:143694595 | A | C | 1 | a0027c0020t0001g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5185+896T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694595 | |||||||
chr4:143694611 | A | G | 2 | a0012c0018t0001g0243 a0012c0018t0001g0244 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5185+880T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694611 | |||||||
chr4:143694683 | C | T | 18 | a0003c0003t0001g0005 a0003c0003t0001g0075 a0003c0003t0001g0077 others(15): Show |
19 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.5185+808G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694683 | |||||||
chr4:143694940 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5185+551G>A | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143694940 | |||||||
chr4:143695008 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5185+483A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695008 | |||||||
chr4:143695022 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5185+469C>T | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695022 | |||||||
chr4:143695167 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00673.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.5185+324T>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695167 | |||||||
chr4:143695213 | A | G | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5185+278T>C | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695213 | |||||||
chr4:143695248 | T | C | 50 | a0001c0006t0001g0006 a0001c0006t0001g0111 a0001c0006t0001g0112 others(47): Show |
53 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.5185+243A>G | FREM3 | ENSG00000183090.5 | transcript | ENST00000329798.5 | protein_coding | 1/7 | chr4 | 143695248 |